Responsible for site management oversight, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. Collaborates with cross-functional teams to manage study milestones, risk mitigation, and clinical project team performance.
The CRA I performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for verifying clinical data accuracy, managing site-level activities, and ensuring patient safety and data integrity throughout the study lifecycle.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with clinical practices and regulatory requirements. Collaborate with cross-functional teams and investigators to manage study operations, documentation, and site progress.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. Collaborate with cross-functional teams and investigators to manage study progress, documentation, and site operations.
The Clinical Research Associate is responsible for the full lifecycle of clinical studies, including site qualification, initiation, monitoring, and close-out visits. They ensure protocol compliance, data integrity, and regulatory adherence while managing site-level activities and communication.
The CRA II/Sr CRA I is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, maintain essential study documentation, and support subject recruitment and retention strategies.
The Clinical Trials Technician provides regulatory support by managing submission documentation, tracking timelines, and maintaining internal databases. They also coordinate site report verification and handle translation requests to ensure project compliance.
The Senior CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and provide guidance to site staff to ensure project objectives and timelines are met.
The Medical Scientist serves as a Clinical Data Reviewer, identifying data errors and performing ongoing reviews of clinical study participant data. They collaborate with cross-functional teams to ensure data quality, manage clinical data queries, and support audit readiness throughout the study lifecycle.
The Director of Clinical Development Operations leads the technical strategy for the FSP Enablement Team and manages clinical operations to ensure quality and efficiency standards are met. They are responsible for line management, process optimization, and ensuring compliance with GCP and ICH guidelines across the business unit.
The Global Study Manager oversees interdisciplinary clinical research programs, ensuring compliance with regulatory requirements and GCP standards. They are responsible for managing project timelines, budgets, and deliverables while acting as the primary liaison between the company and the customer.
The Senior Biostatistician will review statistical analysis plans, develop analysis datasets, and provide statistical support for clinical pharmacology and Phase I studies. They are responsible for validating statistical outputs and ensuring all documentation complies with regulatory and CDISC standards.
Perform ongoing clinical data review to ensure data quality, consistency, and completeness while identifying and resolving discrepancies in EDC systems. Collaborate with cross-functional teams to support data cleaning activities and ensure compliance with GCP and study protocols.
The Senior Statistical Programmer develops custom programming code to generate summary tables, listings, and datasets while ensuring compliance with statistical analysis plans. They also act as a lead programmer, directing team activities and mentoring junior personnel to ensure high-quality deliverables.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, data integrity, and communication to meet project objectives and timelines.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. Collaborate with cross-functional teams and investigators to manage study operations and ensure accurate documentation of monitoring activities.
The Senior Statistical Programmer develops custom code to generate summary tables, listings, and datasets while ensuring quality standards and regulatory compliance. They also act as a lead programmer, directing activities, mentoring personnel, and representing the programming team in sponsor meetings.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure compliance with regulatory standards and study protocols. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the trial lifecycle.
The Clinical Trial Supplies Manager will lead and support clinical supply forecasting and planning systems while optimizing models for clinical studies. They will also manage system configurations, integrations, and cross-functional partnerships to ensure efficient supply execution.
Manage and execute clinical trial-related payments in accordance with contracts, regulatory requirements, and internal procedures. Collaborate with cross-functional teams and study sites to ensure efficient financial operations and timely payment execution.
The Principal Statistical Programmer acts as a lead for a compound or group of studies, maintaining timelines, programming standards, and datasets. They also mentor junior programmers and provide expert solutions to complex technical problems.
The manager oversees data management and pharmacovigilance operations, including line management of staff and ensuring data quality and compliance. They are responsible for project coordination, budget management, and representing the safety department in client and project meetings.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for verifying clinical data accuracy, managing site-level activities, and ensuring subject safety and data integrity.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, maintain clinical data integrity, and provide mentorship to junior staff.
Responsible for site management oversight, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. Collaborates with functional leaders to meet study milestones and manages clinical project team performance and risk mitigation.
The Clinical Data Reviewer performs specialized clinical data reviews ahead of significant project milestones to ensure data readiness and validity. They work as an extension of the clinical scientist to identify inconsistencies, highlight errors, and manage queries across large, multi-faceted data sets.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for verifying clinical data accuracy, managing site-level activities, and ensuring subject safety and data integrity.
The Clinical Research Associate (CRA) is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, maintain accurate clinical data, and act as a primary liaison between the sponsor and study sites.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation.
The Contracts Coordinator will manage project files, study information, and essential document processes while assisting in contract and budget negotiations. They will also provide administrative support to project leads and ensure all study documentation is archived according to company policy.
Perform site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. Manage site-level activities, maintain accurate clinical data, and ensure subject safety throughout the study lifecycle.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out activities to ensure protocol and regulatory compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation.
The CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for managing site-level activities, verifying clinical data accuracy, and maintaining essential study documentation.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation while ensuring patient safety.
The Senior CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The nurse will coordinate and conduct clinical trial visits, ensuring all procedures and assessments are completed according to protocol and SOPs. They are also responsible for accurate data documentation, reporting adverse events, and facilitating the safe handling and administration of trial medication.
The Site Activation Specialist is responsible for managing site activation processes, including regulatory submissions and site selection support at the country level. They also handle contract and budget negotiations while ensuring compliance with project requirements and company SOPs.
The Adult Research Nurse will manage daily trial operations, including protocol adherence, data documentation, and patient assessments. They will also coordinate trial visits, administer medication, and ensure accurate reporting of adverse events while maintaining effective communication with the research team.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the project lifecycle.
The CRA performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Project Data Manager is responsible for overseeing all data management services for assigned projects, ensuring compliance with contractual agreements and sponsor expectations. They act as the functional lead, coordinating team activities, managing project finances, and ensuring all milestones are met according to SOPs and regulations.
The role involves maintaining regulatory compliance for medical documents and representing the editorial group within study teams. It also includes managing project timelines, budgets, and providing technical mentorship to the medical writing staff.
The CRA II/Senior CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject safety and data integrity throughout the study lifecycle.
The role involves negotiating and managing site-specific clinical trial contracts and investigator budgets while ensuring compliance with sponsor requirements. The specialist will also act as a liaison between internal teams, legal departments, and clinical sites to facilitate study start-up and resolve operational issues.
The Customer Contract Manager oversees complex contracts and change order processes while proactively managing budgets and project risks. They serve as the primary customer contact to ensure timely execution of documents and drive revenue targets through effective workload management.
The role involves providing expert guidance on Risk-Based Quality Management (RBQM) and central monitoring activities to ensure clinical trial compliance and data integrity. You will collaborate with cross-functional teams to identify risks, define quality tolerance limits, and oversee the resolution of issues identified through data analytics.
The Research Nurse will conduct clinical trial visits at patient homes and clinical sites, ensuring all procedures follow trial protocols and SOPs. They are responsible for accurate data documentation, administration of trial medication, and reporting adverse events to the project management team.
Design and execute real-world evidence studies using EMR and claims data to support clinical development, HEOR, and regulatory strategy. Collaborate cross-functionally to translate complex analytical results into actionable insights for decision-making.
The Clinical Programmer II designs, writes, validates, and maintains software using tools like SAS, Oracle RDC, and Medidata Rave to meet clinical study specifications. They also lead programming activities, coordinate project deliverables, and provide technical guidance to team members.
The Clinical Trial Supplies Manager leads end-to-end clinical trial supply planning, logistics, and inventory management for assigned studies. They also represent the clinical supply chain on study teams, manage vendor performance, and ensure compliance with regulatory requirements.
The Principal Statistical Programmer will lead programming activities, including the development of SDTM, ADaM, and TLF outputs while ensuring compliance with regulatory standards. They will also mentor junior staff, manage project timelines, and serve as a technical subject matter expert for CDISC requirements.
The Medical Scientist is responsible for ensuring the integrity and quality of clinical data through rigorous safety surveillance and protocol-defined study monitoring. They will assist the lead clinician with data interpretation, safety narrative preparation, and the management of clinical study documentation.
The Clinical Research Associate is responsible for performing site qualification, initiation, monitoring, and close-out activities to ensure protocol and regulatory compliance. They also manage site-level communication, verify clinical data accuracy, and support patient recruitment and retention strategies.
The Project Manager oversees interdisciplinary clinical research studies, ensuring compliance with regulatory standards and contractual agreements. They lead project teams to manage quality, timelines, and budgets while acting as the primary liaison between the company and the customer.
Develop and maintain programs to create analysis datasets, tables, and figures while ensuring accuracy and compliance with statistical standards. Provide comprehensive statistical programming support and collaborate with stakeholders to deliver high-quality outputs.
The Patient Engagement Lead manages global clinical trial recruitment and retention strategies by collaborating with functional leads and solution partners. They are responsible for overseeing project budgets, vendor performance, and ensuring high-quality delivery of patient engagement plans.
The Site Activation Specialist is responsible for managing site activation activities, including regulatory submissions, site selection, and feasibility support. They also oversee contract and budget negotiations while ensuring compliance with project timelines and company SOPs.
The Principal Biostatistician leads biomarker-related statistical activities across clinical studies, serving as the primary contact for sponsors. They are responsible for developing biomarker evaluation plans, conducting advanced data analysis, and mentoring junior staff to ensure high-quality deliverables.
The Senior Medical Writer leads the preparation of complex clinical documents, ensuring scientific accuracy and adherence to regulatory standards. They also coordinate cross-departmental activities, mentor junior staff, and manage client relationships to ensure deliverables are completed on time and within budget.
The role involves managing site activation activities, including regulatory submissions, contract negotiations, and budget management at the country level. It also requires ensuring compliance with SOPs, maintaining Trial Master File documentation, and providing subject matter expertise for clinical trial regulatory processes.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure compliance with regulatory standards and study protocols. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation to support project objectives.
The Principal Biostatistician leads statistical activities across multiple studies, serving as the primary sponsor contact and providing expert consultancy on study design and protocol development. They also oversee project deliverables, mentor junior staff, and ensure compliance with regulatory standards throughout the clinical trial lifecycle.
The Regulatory Consultant will manage and track regulatory submissions while maintaining content plans within Veeva Vault RIM. They will also translate project timelines and coordinate communication between internal teams and regulatory publishing departments.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential documentation while supporting subject safety and data integrity.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The CRA II is responsible for conducting on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. They also contribute to the development of monitoring tools, SOPs, and collaborate with cross-functional teams to support clinical trial operations.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Contract Manager will negotiate and manage clinical trial agreements and site budgets while collaborating with internal stakeholders. They will also track negotiation activities and ensure accurate documentation within sponsor systems.
The Principal Statistical Programmer leads programming activities, develops custom code for clinical trial outputs, and ensures compliance with regulatory standards. They also mentor junior staff, manage project timelines, and serve as a technical subject matter expert for CDISC and regulatory submissions.
The Principal Statistical Programmer leads programming activities, develops custom code for clinical trial outputs, and ensures compliance with regulatory standards like CDISC. They also mentor junior staff, manage project timelines, and serve as a technical subject matter expert for biostatistics teams.
The Clinical Site Support Specialist will manage multi-factor authentication enrollment and troubleshoot technical access issues for clinical trial sites. They will also conduct training sessions and maintain documentation to ensure consistent support quality across various clinical systems.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential trial documentation throughout the study lifecycle.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, maintain accurate clinical data, and ensure subject safety and data integrity throughout the study lifecycle.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Principal Statistical Programmer will lead programming activities for clinical trials, including the development of ADaM datasets, tables, listings, and figures. They will also provide technical expertise, mentor junior staff, and ensure compliance with regulatory standards and project timelines.
The eCOA Project Manager will lead the end-to-end delivery of electronic Clinical Outcome Assessment solutions, serving as the primary liaison between sponsors, internal teams, and vendors. Responsibilities include managing study-specific project plans, overseeing system builds and UAT, and ensuring compliance with regulatory expectations throughout the clinical trial lifecycle.
The Regulatory Associate will build and institutionalize regulatory project management frameworks while providing oversight for GRA-AP portfolios. They will facilitate communication between stakeholders and regulatory teams to ensure project deliverables are met on time.
The Senior CRA will conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. They will also mentor junior staff, develop monitoring tools, and collaborate with cross-functional teams to ensure successful trial execution.
The Senior CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and provide mentorship to junior staff.
The Project Manager provides guidance and daily oversight for the management of international clinical trials, ensuring adherence to budgets and timelines. They also manage CRO interactions, oversee study conduct from start-up to close-out, and coordinate data review processes.
The Central Risk Manager provides subject matter expertise for monitoring strategies and collaborates with cross-functional teams to identify and mitigate project risks. They ensure data quality and integrity through remote data review and statistical monitoring while maintaining compliance with regulatory standards.
The Principal Statistical Programmer develops custom code to generate summary tables, listings, and datasets while ensuring quality standards and regulatory compliance. They also act as a lead, directing programming activities, mentoring personnel, and providing technical expertise on CDISC standards.
The Project Manager will collaborate with cross-functional teams to navigate complex drug development and commercialization processes. They are responsible for understanding customer needs and delivering innovative solutions to ensure project success.
The Site Activation Specialist is responsible for managing site start-up activities, including regulatory submissions, essential document collection, and site contract negotiations. They ensure project timelines are met, monitor financial aspects, and maintain compliance with SOPs and local regulatory requirements.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The Clinical/Medical Scientist will develop medical plans and perform regular medical data reviews to identify risks and trends in clinical study data. They will serve as a primary interface between internal teams and customers to ensure project milestones and data integrity are maintained.
The Senior Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and ensure patient safety and data integrity throughout the study.
The Site Contracts Specialist II manages the end-to-end contract process, including negotiating budgets and agreements for clinical trials. They also provide functional guidance to team members, ensure compliance with SOPs, and collaborate with internal and external stakeholders to facilitate contract execution.
The Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol compliance and data integrity throughout the study lifecycle. They coordinate with cross-functional teams to meet study milestones, manage risks, and oversee the performance of clinical research associates and central monitors.
The Site Payment Specialist manages project files, study information, and financial reporting, including investigator payments and site invoices. They also facilitate internal and external meetings, track key performance indicators, and provide support for audits and quality assurance activities.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The Project Manager II supports the clinical trial operational team by managing CROs and ancillary vendors to ensure study alignment. They are responsible for developing clinical trial documents, including study manuals and Master ICF templates, while overseeing study timelines.
The Medical Scientist will collaborate with cross-functional teams to provide deep expertise and drug development insights to support customer goals. They are responsible for navigating complex drug development processes and delivering innovative solutions within a competitive environment.
The Clinical Project Manager II supports late-phase Hematology and Immunology portfolios by managing operational tasks and liaising with CROs and vendors. They are responsible for developing clinical trial documents, maintaining project team communication, and ensuring study timelines are met.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure compliance with regulatory standards and study protocols. They manage site-level activities, verify clinical data accuracy, and act as a primary liaison between the study site and the project team.
The Site Contracts Lead manages the end-to-end contract process, including drafting, negotiating, and executing clinical trial agreements and budgets. They also provide functional guidance to team members, ensure compliance with SOPs, and act as a liaison between internal departments and external sites.
The Regulatory Labeling Manager will support labeling negotiations with health authorities and interpret safety data to inform labeling updates. They are responsible for preparing labeling components for eCTD submissions and utilizing structured content authoring tools.
The Senior Clinical Project Manager will oversee the development of clinical trial documentation, including protocols and regulatory reports, while managing trial timelines and budgets. They are responsible for site selection, vendor coordination, and implementing risk mitigation and recruitment plans.
The Regulatory Strategist will lead and coordinate regulatory submissions and life-cycle management procedures for Latin American markets. They will act as a local regulatory expert, providing guidance to cross-functional teams and ensuring compliance with regional health authority requirements.
The Site Care Partner performs site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They manage site-level activities, verify clinical data accuracy, and maintain investigator site files throughout the study lifecycle.
The Regulatory Consultant will manage and track regulatory submissions while maintaining content plans within Veeva Vault RIM. They will also coordinate submission activities and translate project timelines into actionable plans using Smartsheet and Microsoft Project.
The Regulatory Labeling Manager is responsible for the development, maintenance, and oversight of labeling content for mature pharmaceutical products. This includes authoring labeling documents, ensuring regulatory compliance, and collaborating with cross-functional teams to align on labeling changes.
The Senior Manager will lead cross-functional regulatory project management activities for global submissions, ensuring compliance with FDA, EMA, and ICH guidelines. They are responsible for managing multiple marketing applications and lifecycle management submissions from initial filing through to final approval.
The Sr Project Specialist manages study documentation, including TMF, regulatory files, and financial reports, while ensuring compliance with clinical research standards. They also facilitate internal and external meetings, track KPIs, and provide support for audits and quality assurance activities.
The Clinical Operations Specialist assists clinical monitoring staff with site management activities and ensures compliance with study protocols and regulatory guidelines. They are also responsible for maintaining the Trial Master File, tracking clinical documentation, and coordinating site supplies.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and act as a primary liaison to ensure project objectives and timelines are met.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The Project Manager II oversees interdisciplinary clinical research studies, ensuring compliance with regulatory requirements and GCP standards. They are responsible for managing project timelines, budgets, and deliverables while acting as the primary liaison between the company and the customer.
The Clinical/Medical Scientist will develop medical plans and perform regular medical data reviews to identify risks and trends in infectious disease studies. They will also serve as a primary interface between internal teams, customers, and vendors to ensure project milestones and quality deliverables are met.
The Executive Director of Strategic Business Development drives enterprise-level sales growth by managing global account strategies and securing high-impact partnerships. They collaborate cross-functionally to develop client-centric solutions and navigate complex procurement environments within the biopharmaceutical sector.
The Director of Business Development is responsible for driving sales growth across a geographic territory by balancing new client acquisition with the expansion of existing accounts. This role involves orchestrating multi-functional solution development and maintaining strong relationships with key stakeholders in the biopharmaceutical industry.
The Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol compliance and data integrity throughout the trial lifecycle. They coordinate with functional teams to meet study milestones, manage risks, and serve as an escalation point for investigator sites.
The Site Monitoring Lead is responsible for overseeing clinical monitoring, site management, and central monitoring deliverables to ensure patient safety and regulatory compliance. They manage study risks, coordinate with functional teams, and provide leadership to CRAs and Central Monitors to meet study milestones.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, oversee data integrity, and provide mentorship to junior staff.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Principal Global Feasibility Lead independently manages complex RFP and feasibility objectives across all therapeutic areas while collaborating with internal and external stakeholders. They are responsible for delivering high-quality site-level feasibility assessments, mentoring junior staff, and developing departmental metrics and processes.
The Senior Clinical Research Associate II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and act as a primary liaison to ensure project objectives and timelines are met.
The Medical Scientist works with the Medical Director to develop medical plans and perform regular medical data reviews to identify risks and trends. They also serve as the primary interface between internal teams, customers, and vendors to ensure project milestones and quality deliverables are met.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The CRA II is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and act as a primary liaison with study site personnel.
The specialist administers contract management processes, including negotiating budgets and agreements for clinical trials at a project level. They also collaborate with internal and external stakeholders to ensure compliance with timelines, quality standards, and regulatory requirements.
The Site Contracts Specialist II manages the end-to-end contract process for clinical trials, including drafting, negotiating, and executing site-specific agreements and budgets. They also provide functional guidance to internal teams, mentor junior staff, and ensure compliance with SOPs and project timelines.
Develop and validate SDTM/ADaM datasets and TLFs while supporting safety and efficacy analyses for clinical trials. Lead cross-functional teams and contribute to e-submissions ensuring full CDISC compliance.
The medical scientist will collaborate with cross-functional teams to shape solutions that meet customer needs throughout the drug development and commercialization continuum. They are expected to take initiative and challenge the status quo to drive patient progress and customer success.
The Project Manager is responsible for overseeing trial master file management, coordinating study deliverables across departments, and managing vendor relationships. They also handle financial reporting, risk mitigation strategies, and facilitate team training to ensure project milestones are met.
The Project Manager II oversees interdisciplinary clinical research studies, ensuring compliance with regulatory standards and contractual agreements. They are responsible for managing project timelines, budgets, and deliverables while acting as the primary liaison between the company and the customer.
The role involves overseeing the site activation process, managing regulatory submissions, and ensuring quality deliverables at the country level. It also includes supporting site selection, contract negotiation, and maintaining regulatory intelligence in compliance with SOPs.
The role involves leading the preparation of complex regulatory medical writing deliverables while ensuring scientific accuracy and adherence to regulatory standards. The writer will coordinate cross-functional activities, mentor junior staff, and manage client relationships throughout the document development process.
The Research Nurse will coordinate and conduct clinical trial visits, ensuring all procedures and assessments are completed according to protocol and SOPs. They are responsible for maintaining accurate documentation, managing trial medication, and reporting adverse events to the project team.
The Principal Statistician serves as a department resource, mentoring biostatisticians and overseeing the development of statistical analysis plans and project deliverables. They act as a lead biostatistician on clinical trials, ensuring high-quality output and compliance with regulatory standards throughout the project lifecycle.
The Site Activation Specialist is responsible for managing site start-up activities, including regulatory submissions, contract negotiations, and budget management at the country level. They ensure compliance with SOPs and project requirements while tracking milestones and providing contingency plans for potential delays.
The Project Data Manager will collaborate with cross-functional teams to deliver clinical solutions and support drug development processes. They are responsible for managing project data while ensuring compliance with industry standards and customer requirements.
The Research Nurse will manage day-to-day trial activities, including protocol compliance, data documentation, and patient assessments. They are also responsible for administering trial medication, processing samples, and reporting adverse events to the project team.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for managing site activities, verifying clinical data accuracy, and maintaining essential study documentation.
Provides medical oversight for clinical studies, serving as the primary medical contact and ensuring subject safety. Contributes to protocol development, pharmacovigilance, and the analysis of clinical data to mitigate study risks.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and ensure the safety and confidentiality of study subjects.
The Project Manager oversees interdisciplinary clinical research studies, ensuring compliance with regulatory requirements and GCP standards. They are responsible for managing project timelines, budgets, and deliverables while acting as the primary liaison between the company and the customer.
The specialist manages the end-to-end contract process for clinical trials, including drafting, negotiating budgets, and coordinating with legal and clinical teams. They also provide mentorship to junior staff and ensure compliance with departmental SOPs and project timelines.
The Senior Central Risk Manager provides subject matter expertise for monitoring strategies and collaborates with cross-functional teams to identify and mitigate project risks. They ensure compliance with protocols, ICH/GCP standards, and regulatory requirements while managing study deliverables and budget expectations.
The specialist is responsible for processing and triaging Individual Case Safety Reports (ICSRs) while ensuring data accuracy and regulatory compliance. They also perform medical coding, literature screening, and maintain safety tracking systems in accordance with global regulations.
Responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety and regulatory compliance. Collaborates with functional leaders to coordinate study milestones and ensures the clinical team adheres to protocol and risk mitigation strategies.
The specialist manages resource solutions for specific roles, ensuring data integrity within global resourcing tools and trackers. They analyze capacity and skillsets to support assignment recommendations and facilitate communication between internal stakeholders and business units.
The Senior Data Analyst will conduct longitudinal cohort studies and perform complex data analyses using SAS or R. They are responsible for assessing data quality, reviewing protocols, and ensuring adherence to data standards.
Administers contract management processes including negotiating budgets and contracts for clinical trials while ensuring compliance with protocols and legal standards. Collaborates with internal and external stakeholders to facilitate contract execution and provides functional guidance to team members.
The Regulatory Manager will lead regulatory activities, including the preparation of technical submissions and management of project timelines and budgets. They will act as a subject matter expert, providing strategic guidance and oversight to team members while ensuring compliance with global regulatory requirements.
The Principal Medical Writer leads the development of complex medical writing deliverables and manages documentation strategy across clinical studies. They also mentor junior staff, ensure compliance with regulatory standards, and collaborate with cross-functional teams to meet client objectives.
The Principal Medical Writer leads the development of complex clinical and regulatory documents while ensuring scientific accuracy and adherence to regulatory standards. They also manage document strategy, mentor junior staff, and collaborate with cross-functional teams to meet client objectives.
The Associate Director will oversee central monitoring activities to ensure clinical trial success and operational excellence. They will collaborate with cross-functional teams to shape solutions that meet customer needs and drive patient progress.
The CRA II is responsible for conducting on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. They also contribute to the development of monitoring tools, SOPs, and collaborate with cross-functional teams to support clinical trial operations.
The Senior Clinical Trial Operations Specialist will manage project files, regulatory documentation, and study information while ensuring effective communication across the project team. They will also provide administrative support to project leads and assist with quality assurance activities, including audit preparation and documentation.
The Project Data Manager acts as the functional lead for data management, coordinating team activities and ensuring project milestones are met according to SOPs and regulations. They are also responsible for financial management, resource planning, and maintaining project documentation to support internal and external audits.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the clinical trial lifecycle.
The Global Trials Optimization Specialist manages program feasibility, recruitment, and retention planning to ensure successful clinical trial enrollment. They partner with cross-functional teams to identify enrollment challenges, monitor performance, and implement mitigation strategies throughout the trial lifecycle.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and maintain investigator site files while ensuring subject safety and data integrity.
The Clinical Trial Lead manages interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while overseeing project timelines and budgets. They act as the primary liaison between the company and the customer to facilitate successful study launch, conduct, and closeout.
The Site Contracts Lead oversees the negotiation of clinical study agreements and investigator budgets while serving as a subject matter expert for internal and sponsor stakeholders. They are responsible for establishing contract execution strategies, managing escalations, and mentoring team members to ensure compliance with organizational standards.
The Clinical Trial Leader is responsible for the end-to-end set-up, execution, and delivery of assigned clinical trials while ensuring compliance with GCP and regulatory standards. They lead interdisciplinary teams, manage project budgets, and act as the primary liaison between the company and the customer.
The Site Contracts Specialist manages the negotiation and preparation of contracts and budgets for clinical trials, ensuring alignment with sponsor requirements. They also coordinate with internal and external stakeholders to streamline contract processes and maintain compliance with departmental SOPs.
The specialist will process and triage Individual Case Safety Reports (ICSRs) while ensuring data accuracy and regulatory compliance within safety databases. They will also perform literature screening, MedDRA coding, and maintain documentation for clinical trials and post-marketing programs.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the project lifecycle.
The Project Manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while managing project timelines and budgets. They act as the primary liaison between the company and the customer to facilitate study launch, conduct, and closeout.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure compliance with regulatory standards and study protocols. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the trial lifecycle.
Administer all contract management processes, including negotiating and preparing contracts, budgets, and related documents for clinical trials. Collaborate with internal and external legal, finance, and clinical operations departments to ensure compliance and timely execution of agreements.
The Clinical Trial Lead provides leadership and management for global clinical trials, ensuring quality execution and compliance with GCP and regulatory standards. They act as the primary liaison between the company and the customer while managing project budgets, timelines, and interdisciplinary teams.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Senior Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol compliance and data integrity. They lead clinical project teams, manage study risks, and coordinate with functional leaders to meet study milestones and deliverables.
Provide leadership to clinical operations within the APAC region to ensure the overall delivery and performance of clinical trials. Collaborate with cross-functional teams to navigate drug development complexities and meet customer goals.
The Senior Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The biostatistician will design and execute real-world evidence studies using EMR and claims data to support clinical development, HEOR, and regulatory strategy. They will apply robust statistical methodologies and collaborate cross-functionally to translate complex analytical results into actionable insights.
The Site Contracts Manager will negotiate and manage clinical trial budgets and agreements with academic institutions and clinical sites. They will also lead contracting projects, ensure compliance with GCP, and proactively manage risks to maintain study timelines.
The Senior Site Contracts Specialist manages the site identification process, including negotiating confidentiality agreements and site information forms. They also monitor site performance metrics and serve as the primary point of contact for investigative sites to ensure project compliance.
Leads the clear and accurate completion of medical writing deliverables while coordinating activities across departments. Manages document reviews, ensures adherence to regulatory standards, and mentors less experienced writers on complex projects.
The lead statistical programmer develops custom code for clinical trial outputs and ensures compliance with regulatory standards like CDISC. They also mentor junior staff, manage project timelines, and act as a technical subject matter expert for statistical programming activities.
The Principal Medical Writer leads the preparation of complex regulatory medical writing deliverables while ensuring scientific accuracy and adherence to regulatory standards. They also coordinate cross-functional reviews, mentor junior staff, and maintain strong relationships with clients and internal departments.
The manager provides leadership for the operational and financial aspects of clinical trial supplies throughout the project life cycle. They are responsible for vendor management, inventory planning, and ensuring compliance with regulatory standards and study requirements.
The Clinical Operations Specialist is responsible for ensuring site compliance with clinical protocols and maintaining accurate trial documentation. They also assist clinical monitoring staff with site management activities and coordinate essential project supplies and team meetings.
The Senior Project Manager oversees interdisciplinary clinical research programs, ensuring compliance with regulatory requirements and GCP standards. They act as the primary liaison between the company and customers to manage project deliverables, timelines, and budgets.
The Clinical Project Manager will lead the end-to-end execution of complex Phase 2b inflammation studies, managing timelines, deliverables, and cross-functional teams. They are responsible for vendor oversight, risk mitigation, and ensuring all study documentation and operational milestones are met from start-up through closeout.
The project manager will lead the execution of oncology and cell & gene therapy trials from startup through closeout while serving as the primary point of contact for sponsors. They are responsible for managing study timelines, budgets, regulatory compliance, and cross-functional team coordination to ensure inspection readiness.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and provide mentorship to junior staff while maintaining study timelines and budgets.
The Senior/Principal Medical Editor manages complex medical writing projects while ensuring documents meet regulatory standards and internal quality requirements. They also provide technical expertise, mentor staff, and contribute to process improvement initiatives.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and data integrity. They manage site-level activities, verify informed consent, and ensure accurate clinical data capture while maintaining regulatory standards.
The Research Nurse will manage daily trial operations, including protocol adherence, data documentation, and subject visits. They are responsible for administering trial medication, processing samples, and reporting adverse events to the project management team.
The Project Financial Analyst II supports the Business Unit Controller by managing revenue recognition, project budgets, and financial forecasting within Oracle. They are responsible for drafting variance analysis reports, conducting project close-out reconciliations, and monitoring the overall financial health of assigned projects.
The Principal Statistician oversees biostatistics personnel, develops training plans, and ensures the timely delivery of high-quality statistical outputs for clinical trials. They act as a lead biostatistician, collaborating with sponsors and regulatory agencies while ensuring compliance with SOPs and ICH guidelines.
The statistician provides support across the project lifecycle, from protocol development to clinical study reports, while coordinating biostatistics and programming activities. They serve as a biostatistics representative on project teams, ensuring high-quality deliverables and adherence to regulatory standards.
The Medical Writer II performs end-to-end scientific writing, including managing publication plans and ensuring documents are MLR-ready for submission. They also mentor less experienced writers and collaborate across departments to ensure document accuracy and regulatory compliance.
The Medical Writer II manages end-to-end scientific writing workflows, including publication planning and Veeva Vault document management. They also mentor less experienced writers and ensure all deliverables meet regulatory and client standards.
The Project Financial Analyst II is responsible for preparing, reconciling, and analyzing business unit revenue, contracts, and project metrics. They support the Business Unit Controller by drafting financial forecasts, variance analyses, and ensuring accurate reporting within established timelines.
The Principal Medical Writer leads the development of complex clinical documents and manages medical writing activities across various studies. They also provide expert peer reviews, mentor junior staff, and ensure all deliverables meet regulatory and client standards.
The Clinical Research Associate (CRA) will perform site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They are responsible for managing site activities, verifying clinical data accuracy, and maintaining essential study documentation.
The role involves copyediting and performing quality reviews on complex medical documents to ensure compliance with regulatory standards. Additionally, the editor will lead project deliverables, mentor staff, and provide technical expertise to cross-departmental study teams.
The Clinical Scientist collaborates with the Medical Director to develop medical plans and perform rigorous medical data reviews to identify risks and trends. They serve as the primary interface between internal teams and customers to ensure project milestones and quality deliverables are met.
The project manager oversees medical writing deliverables, manages cross-functional teams, and ensures high-quality work products. They also supervise staff, handle performance reviews, and support business development activities such as proposal and budget preparation.
The Senior Medical Writer leads the preparation of complex clinical documents while ensuring scientific accuracy and adherence to regulatory standards. They coordinate cross-functional activities, mentor junior staff, and manage client relationships to ensure deliverables are completed on time and within budget.
The Principal Research Scientist is responsible for developing, validating, and optimizing bioanalytical methods while coordinating laboratory activities. They also supervise and mentor scientific staff to ensure compliance with corporate policies and operational objectives.
The role involves administering contract management processes and negotiating budgets and agreements for industry-sponsored clinical trials. It also requires coordinating with legal and clinical operations teams to ensure the accurate execution and archival of Clinical Trial Agreements.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves managing project milestones, budgets, and ensuring protocol and GCP compliance while leading clinical team members.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves managing clinical project teams, tracking study progress against milestones, and ensuring regulatory compliance and data integrity.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves tracking study progress against milestones, managing resource allocation for CRAs, and ensuring regulatory compliance and data integrity.
Leads the creation and accurate completion of medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinates with cross-functional teams and clients to ensure scientific clarity and adherence to regulatory standards.
Leads the creation and completion of high-quality medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinates with cross-functional teams and clients to ensure scientific accuracy and adherence to regulatory standards.
The role is responsible for overseeing site management, clinical monitoring, and regulatory compliance to ensure patient safety and data integrity. It involves coordinating with functional leaders to meet study milestones and managing the performance of CRAs and Central Monitors.
Lead the migration to SAS Viya and provide high-level technical expertise in statistical programming to generate summary tables, listings, and datasets. Mentor team members and ensure all deliverables comply with industry standards and regulatory requirements.
The role involves developing custom SAS code to generate summary tables, listings, and datasets according to statistical analysis plans. As a lead programmer, the candidate will direct programming activities, ensure quality standards, and mentor junior personnel.
The role involves creating and updating payment trackers and processing invoices and payments within the GMS system. Additionally, the specialist manages patient reimbursement costs and provides mentoring to junior payment CTAs.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File and Trial Master File.
The CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.
Lead pre-award strategy and commercial leadership for Real World Late Phase (RWLP) accounts, including RFP strategy and budget structures. Serve as the strategic account leader post-award to maintain portfolio performance and sustain senior-level sponsor relationships.
The role involves executing global regulatory CMC strategies and preparing documentation for small molecule products. It also provides regulatory guidance to cross-functional teams to ensure compliance with global requirements.
Provides medical oversight and monitoring for clinical studies in immunology and rheumatology, including protocol design and drug safety input. Leads medical responses for proposals and mentors staff on therapeutic research principles.
The role focuses exclusively on processing and reviewing safety documents within the Trial Master File (TMF) system. Responsibilities include ensuring document completeness, indexing accuracy, and collaborating with study owners to resolve discrepancies.
The Regulatory Device CMC Manager supports strategies for marketed and development products by preparing and submitting regulatory CMC documentation for combination devices. The role provides guidance to cross-functional teams to ensure global regulatory requirements are integrated into development and commercial programs.
The role involves serving as a statistical resource to mentor biostatisticians and oversee the preparation of Statistical Analysis Plans and clinical study reports. Additionally, the position focuses on maintaining R-based computing environments and developing Rshiny applications for data visualization.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and maintain the Investigator Site File and Trial Master File.
The role involves coordinating clinical trial visits and administering trial medications while ensuring accurate data collection in Case Report Forms. The nurse will also manage sample dispatch and report adverse events in compliance with SOPs and GCP guidelines.
Develop custom programming code using SAS to generate summary tables, listings, and datasets according to statistical analysis plans. Act as the lead statistical programmer by directing personnel, reviewing project documentation, and ensuring quality standards are met.
Provide statistical support to the Medical Affairs group focusing on exploratory analysis, observational studies, and real-world evidence. Manage the statistical lifecycle of projects from protocol development to the final clinical study report.
Oversee site management, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. Coordinate with functional leaders to meet study milestones and manage the clinical project team's contractual obligations.
Administers all contract management processes for clinical trials, including negotiating budgets and preparing agreements for investigators and vendors. Collaborates with legal and finance departments to ensure compliance with timelines and quality standards.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain essential study documentation.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.
Lead the operational and financial delivery of global clinical projects from proposal to final deliverables. Act as the primary liaison between the company and customers while managing interdisciplinary teams and ensuring regulatory compliance.
Manage quality assurance and regulatory compliance within the clinical solutions team to accelerate drug development. Collaborate with cross-functional teams to ensure customer success and adherence to healthcare regulations.
The role involves coordinating and completing clinical trial visits both on-site and off-site while ensuring strict adherence to protocols and SOPs. Responsibilities include administering trial medication, processing samples, and accurately reporting adverse events.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, data integrity, and subject safety for Real World Late Phase studies.
Provides medical oversight and monitoring for assigned clinical studies, serving as the primary medical contact for customers. Responsible for protocol design, drug safety oversight, and delivering therapeutic training to project teams.
Develop custom SAS programming code to generate summary tables, listings, and datasets according to statistical analysis plans. Act as a lead statistical programmer by directing activities, reviewing project documentation, and ensuring CDISC compliance.
The role is responsible for preparing SR&ED tax incentive claims and leading income and indirect tax audits. It also involves managing monthly, quarterly, and year-end closes while ensuring compliance with US and Canadian GAAP and Sarbanes-Oxley controls.
The Regulatory CMC Manager supports global regulatory CMC strategies for cell and gene therapy products during development and commercialization. This includes preparing regulatory documentation and providing guidance to cross-functional teams on compliance and GMP investigations.
The role involves performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires managing site-level activities, verifying clinical data integrity, and overseeing investigational product inventory.
Lead and manage Site Start-Up (SSU) deliverables globally or regionally to ensure study sites are activation-ready on time and within budget. Oversee the entire lifecycle from site selection and regulatory submissions to the collection of essential documents.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for verifying clinical data integrity, managing investigational products, and maintaining the Trial Master File.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.
The CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.
The CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and provide guidance to site staff and junior CRAs.
The Employee Wellness Specialist focuses on enhancing employee well-being within a global life sciences services organization. The role involves collaborating with diverse teams to support a healthy and inclusive corporate culture.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory requirements. Develop quality monitoring tools and collaborate with cross-functional teams to support smooth clinical trial operations.
Lead the scientific oversight of eCOA implementation and manage the licensing, translation, and integrity of clinical outcome assessment scales. Design and deliver rater training programs to ensure standardized endpoint data collection across clinical sites.
Responsible for hiring, managing, and developing biostatisticians while ensuring projects meet timelines, budgets, and quality standards. The role involves overseeing staff performance, mentoring associates, and managing client relationships to ensure successful project execution.
The role involves leading statistical activities across the clinical trial lifecycle, from protocol development to the final clinical study report. Responsibilities include mentoring biostatisticians, overseeing SAP preparation, and managing regulatory submission requirements.
The role involves coordinating and completing subject trial visits both on- and off-site while ensuring adherence to trial protocols and SOPs. Responsibilities include administering trial medication, processing samples, and accurately reporting adverse events.
Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manage project scope and deliverables while interfacing between internal teams, customers, and vendors to ensure data integrity and subject safety.
Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manage project scope and serve as the primary interface between internal teams, customers, and vendors regarding eligibility and data review.
Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manage project scope and deliverables while interfacing between internal teams, customers, and vendors to ensure data integrity and subject safety.
Collaborates with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manages project scope and serves as the primary interface between internal teams, customers, and vendors regarding eligibility and data review.
Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manage project scope and deliverables while interfacing between internal teams, customers, and vendors to ensure data integrity and subject safety.
Develop programs and provide statistical support for epidemiologists to source, organize, and interpret complex real-world data sets. Create analysis datasets, tables, and figures while ensuring outputs meet quality standards and protocol requirements.
Manage interdisciplinary clinical research studies ensuring compliance with GCP, SOPs, and regulatory requirements. Act as the primary liaison between the company and customers to oversee study launch, conduct, closeout, and financial performance.
Manage interdisciplinary clinical research studies ensuring compliance with GCP, SOPs, and regulatory requirements. Act as the primary liaison between the company and customers to oversee study launch, conduct, closeout, and financial performance.
The Study Manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while managing timelines and budgets. They act as the primary liaison between the company and the customer to ensure successful study launch, conduct, and closeout.
The Study Manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while managing timelines and budgets. They act as the primary liaison between the company and the customer to ensure successful study launch, conduct, and closeout.
Manage interdisciplinary clinical research studies in oncology, ensuring compliance with GCP and regulatory requirements. Act as the primary liaison between the company and customers to oversee study launch, conduct, and financial performance.
Manage interdisciplinary clinical research studies ensuring compliance with GCP and regulatory requirements while acting as the primary liaison for customers. Lead project teams to oversee quality, timelines, budget management, and the completeness of the Trial Master File.
Support the setup and maintenance of CTMS and TMF while managing study budgets and external service provider coordination. Perform central monitoring and data oversight to ensure the consistency and correctness of clinical study data.
Lead the negotiation and preparation of contracts and budgets for industry-sponsored clinical trials. Coordinate with legal, finance, and clinical operations to ensure accurate execution and archival of site-specific agreements.
The Director of Business Development is responsible for driving sales growth in a specific geographic territory through a mix of new client acquisition and existing account expansion. This involves developing tailored engagement plans and collaborating with cross-functional teams to deliver integrated life sciences solutions.
The Director of Business Development will lead initiatives to accelerate customer success in drug development and commercialization. This role involves collaborating with various teams to navigate complexities and drive impactful solutions for healthcare.
Lead business development efforts across the West Coast region to accelerate customer success in the life sciences sector. Partner with innovators to navigate the drug development and commercialization continuum.
The Clinical Assessment Scientist will act as a COA Lead, collaborating with cross-functional teams to deliver clinical solutions for drug development projects. They will apply therapeutic expertise to understand customer needs and drive progress across the drug development continuum.
The Senior Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for verifying clinical data accuracy, managing site staff performance, and ensuring the safety and integrity of clinical trial data.
The Director serves as a scientific subject matter expert in immunology, providing oversight for clinical trials and leading the development of global business opportunities. They coordinate with project managers to ensure study quality, manage budgets, and facilitate scientific advisory boards while producing technical reports and manuscripts.
The Director serves as a scientific subject matter expert in virology, providing oversight for clinical trials and leading the development of project proposals and bid defenses. They coordinate with project managers to ensure study quality, timelines, and budgets while facilitating scientific advisory boards and authoring industry publications.
The role serves as a scientific subject matter expert in oncology clinical trials, providing oversight for project proposals, study start-up, and ongoing management. It involves collaborating with business development to win global opportunities and leading the development of scientific reports, manuscripts, and study documentation.
Responsible for site management oversight, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. Collaborates with cross-functional teams to manage study milestones, risk mitigation, and clinical trial documentation.
The Clinical Trial Manager oversees site management, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. They also manage study risks, coordinate with functional teams, and ensure adherence to contractual obligations and study timelines.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site performance, verify clinical data accuracy, and ensure patient safety and data integrity throughout the study.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory guidelines. Collaborate with cross-functional teams and investigators to support clinical trial operations and maintain accurate documentation.
The role involves using SAS or other software to develop custom programming code for generating summary tables, data listings, graphs, and derived datasets according to the statistical analysis plan and specifications. Responsibilities also include performing validation programming, ensuring outputs meet quality standards, and managing project timelines while acting as the lead statistical programmer.
The role involves performing site qualification, initiation, monitoring, management, and close-out visits while ensuring compliance with regulatory standards like ICH-GCP and protocol requirements. Key duties include evaluating site performance, managing data integrity via Source Document Review and query resolution, and maintaining essential study documentation.
The role involves performing all stages of site monitoring, including qualification, initiation, interim monitoring, management, and close-out visits, ensuring strict adherence to regulatory guidelines like ICH-GCP and protocol compliance. Key duties include evaluating site performance, verifying data accuracy via Source Document Review, managing query resolution, and ensuring proper handling and documentation of the Investigational Product.
The role involves performing site qualification, initiation, monitoring, management, and close-out visits, ensuring compliance with regulatory standards like ICH-GCP and protocol requirements. Responsibilities also include evaluating site performance, managing data integrity through source document review and query resolution, and maintaining essential study documentation.
The CRA II performs site qualification, initiation, monitoring, management, and close-out visits ensuring compliance with regulatory standards like ICH-GCP and protocol requirements. Responsibilities also include evaluating site performance, verifying informed consent, assessing patient safety and data integrity, and managing essential study documentation.
The job description focuses heavily on the company's mission, culture, and commitment to accelerating therapy delivery rather than listing specific IMS Specialist I tasks. The role is situated within a fully integrated biopharmaceutical solutions organization focused on clinical, medical affairs, and commercial insights.
The Clinical Research Associate (CRA) will perform site qualification, initiation, monitoring, and close-out visits, ensuring compliance with regulatory and protocol standards. They will assess site performance, manage site-level activities, and support patient recruitment and retention strategies.
The Principal Biostatistician serves as a resource for the statistical department, mentoring biostatisticians and overseeing training plans. They provide support across all statistical tasks during the project lifecycle and ensure high-quality work is completed on time.
The Sr CRA is responsible for site qualification, initiation, monitoring, and close-out visits, ensuring compliance with regulatory and protocol standards. They will assess site performance, manage site-level activities, and support patient recruitment and retention strategies.
The CRA II is responsible for performing site qualification, initiation, monitoring, and close-out visits, ensuring compliance with regulatory and protocol standards. They will also assess site performance and communicate any serious issues to the project team while supporting patient recruitment and retention strategies.
