The Senior Clinical Research Associate manages the full site monitoring lifecycle, ensuring compliance with GCP, protocols, and regulatory requirements. They also act as a Lead CRA to coordinate global studies, mentor junior staff, and partner with project teams to ensure study milestones are met.
Provide high-level administrative support to C-suite executives, including complex calendar management and international travel coordination. Facilitate seamless day-to-day operations by managing business correspondence, organizing events, and maintaining strong relationships with global stakeholders.
Lead the full contract lifecycle, including negotiation of sponsor agreements, change orders, and amendments. Collaborate with cross-functional teams to ensure alignment on project scope, budgets, and financial requirements.
Lead and oversee study start-up and site activation activities while serving as the primary point of accountability for assigned projects. Drive cross-functional collaboration to ensure milestones are met on time and within budget while managing site activation metrics and risks.
Lead pharmacovigilance teams and oversee global clinical trial projects, ensuring regulatory compliance and delivery within agreed timelines, quality expectations, and scope. Develop staff, resolve operational and study issues, support project planning and sponsor audits, and contribute to training and departmental initiatives.
Lead pharmacovigilance projects and teams, ensuring compliant safety activities and delivery against quality, timeline, budget, and scope expectations. Develop team members, advise on safety regulations and best practices, and contribute to audits, proposals, SOPs, and operational improvement initiatives.
Lead global pharmacovigilance projects and teams, ensuring compliant, high-quality delivery while overseeing performance, risks, complex safety reporting, and sponsor requirements. Improve departmental processes and technology, develop staff, support proposals and business development, and represent the function in audits and client engagements.
The Clinical Trials Associate provides administrative and project-tracking support to clinical project teams to ensure documentation and activities are accurate and timely. Responsibilities include managing system access, maintaining project portals, and coordinating training for team members.
The In-House Clinical Research Associate I supports site management activities throughout the study lifecycle, ensuring compliance with Good Clinical Practice and regulatory requirements. They collaborate with cross-functional teams to manage study documentation, support remote monitoring, and facilitate site engagement.
Support site management activities throughout the clinical study lifecycle, including study initiation, remote monitoring, and close-out. Collaborate with clinical trial managers and field CRAs to ensure site documentation, data quality, and study deliverables remain on schedule.
Manage clinical research activities at investigative sites from site selection and study start-up through monitoring and closeout, including conducting PSSVs, SIVs, IMVs, and COVs. Train and support site personnel while ensuring protocol adherence, regulatory compliance, participant safety, data quality, and effective site performance.
The Sales Development Account Manager will drive customer acquisition by generating new business opportunities through inbound lead qualification and outbound prospecting. They will collaborate with Business Development and Marketing teams to build a strong pipeline and advance prospects through the early stages of the sales cycle.
The manager will oversee post-award site identification activities, including feasibility strategies, site outreach, and recommendation processes. They are also responsible for training assigned resources and providing oversight to Site Activation Specialists.
The Senior Project Manager is responsible for the end-to-end coordination and management of clinical trials from start-up through closeout. They direct the technical, financial, and operational aspects of projects to ensure deliverables meet quality, time, and cost expectations.
Manage research activities at investigative sites throughout the full study lifecycle, including start-up, maintenance, and close-out. Ensure site compliance with regulatory requirements, informed consent, and accurate data collection while maintaining effective communication with study teams.
Manage clinical research activities at investigative sites from site selection and study start-up through monitoring and closeout. Train and support site personnel, oversee compliance and safety reporting, and collaborate with sites and study teams to ensure data quality and successful study delivery.
Set the enterprise clinical innovation strategy and roadmap, prioritizing automation, AI, analytics, and workflow initiatives and leading experiments from opportunity definition through evidence-based scale decisions. Develop business cases and value measures, support implementation and adoption, establish responsible innovation governance, and build reusable methods across clinical development.
The Site Activation Manager is responsible for coordinating and overseeing site identification, essential document collection, and contract status for clinical trials. They serve as the primary point of contact for study start-up activities, ensuring projects are delivered on-time and within budget while maintaining regulatory compliance.
Medically manage assigned clinical trials, including global or pan-regional studies, and provide medical review and support for serious adverse events. Contribute medical and scientific expertise to training, study and protocol design, feasibility and business development, study documentation, regulatory compliance, and mentoring.
The Senior Legal Contract Manager will lead the review, negotiation, and management of complex commercial contracts, including Master Services Agreements and Confidential Disclosure Agreements. They will collaborate with cross-functional teams to identify risks, ensure alignment with business objectives, and manage the full contract lifecycle from intake to execution.
The Payroll Accountant will manage global payroll-related financial information, including journal entries, reconciliations, and month-end reporting. They will also investigate discrepancies, support year-end audits, and contribute to process improvement initiatives.
The Associate Manager will lead and oversee Risk-Based Quality Management (RBQM) activities and develop Central Monitoring Plans for clinical trials. They will collaborate with cross-functional teams to identify risks, analyze data trends, and ensure study execution meets regulatory and quality standards.
The Clinical Trials Associate provides administrative and project coordination support to global teams to ensure study activities remain on track. Responsibilities include managing project documentation, maintaining portals, and coordinating team training and meeting logistics.
The Feasibility Specialist will analyze data to develop site identification strategies and manage feasibility outreach activities. They will also collaborate with cross-functional teams to ensure high-quality study planning and process improvement.
You will lead vendor performance oversight, risk management, and continuous improvement initiatives to ensure high-quality clinical trial delivery. This involves collaborating with cross-functional teams to monitor vendor compliance, resolve performance issues, and implement effective governance strategies.
The Site Activation Manager leads study start-up and site activation activities by coordinating cross-functional teams to ensure milestones are met on time and within budget. They serve as the primary point of contact for stakeholders, managing documentation, risk assessments, and performance metrics to ensure clinical sites are ready for patient enrollment.
The In-House Clinical Research Associate supports clinical study delivery by ensuring compliance with GCP and regulatory requirements. They manage site documentation, conduct remote monitoring activities, and coordinate communication between sites and project teams.
The Senior Clinical Trial Associate supports clinical study delivery by managing documentation, tracking project activities, and ensuring compliance with regulatory standards. They collaborate with cross-functional teams to maintain project portals, prepare site files, and facilitate effective communication across study operations.
Manage research activities at investigative sites throughout the clinical study lifecycle, including start-up, maintenance, and closeout. Ensure study compliance with regulatory requirements, informed consent, and safety reporting while collaborating with study teams.
The Senior Project Manager leads cross-functional teams to deliver Phase I-IV clinical trials from start-up through closeout. They are responsible for managing project timelines, budgets, and quality while serving as the primary point of contact for clients.
The Regional Finance Manager will ensure financial governance, compliance, and operational excellence across multiple countries in the region. They will partner with leadership to provide financial insights, manage outsourced service providers, and drive process improvements.
Lead the end-to-end delivery of Phase I-IV clinical trials, ensuring projects meet quality, budget, and timeline objectives. Coordinate cross-functional teams, clients, and external partners while managing project risks and operational challenges.
Manage clinical research activities at investigative sites, including site selection, study start-up, and conducting various monitoring visits. Ensure protocol adherence, regulatory compliance, and high-quality data collection while providing leadership and support to site personnel.
Manage clinical research activities at investigative sites, including site selection, study start-up, and conducting various monitoring visits. Ensure protocol adherence, regulatory compliance, and high-quality data collection throughout the clinical trial lifecycle.
Lead the coordination, preparation, and delivery of complex proposals, RFIs, and pricing analyses for clinical research programs. Collaborate with cross-functional teams to ensure high-quality submissions while providing mentorship and process improvement support.
Lead and coordinate clinical site management activities from study startup through closeout while ensuring quality, compliance, and operational excellence. Partner with project management and cross-functional teams to drive study performance, mitigate risks, and support site recruitment strategies.
The Specialist will lead regulatory compliance activities and manage essential study documentation to ensure quality standards are met before site activation. They will collaborate with cross-functional teams to drive consistency and efficiency throughout the clinical research study start-up process.
The Project Analyst manages the financial health of projects by tracking actuals, forecasting revenue, and ensuring profitability. They act as the financial expert for client interactions and collaborate with project teams to maintain accurate financial data.
The Associate Manager will lead and oversee Risk-Based Quality Management (RBQM) activities, including the development of central monitoring plans and the tracking of key risk indicators. They will collaborate with cross-functional teams to identify and mitigate study risks while ensuring compliance with ICH GCP guidelines.
Manage clinical research activities at investigative sites, including site selection, study start-up, and various monitoring visits. Ensure protocol adherence, regulatory compliance, and high-quality data collection throughout the clinical trial lifecycle.
The Senior CRA manages clinical research activities at investigative sites, ensuring high standards of quality, patient safety, and regulatory compliance. They conduct various monitoring visits, train site personnel, and drive data quality throughout the clinical trial lifecycle.
The Senior Clinical Research Associate is responsible for managing research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety protocols while conducting study initiation visits and managing site activities remotely.
The Senior Associate will lead pharmacovigilance activities for clinical studies, including the collection, evaluation, and reporting of serious adverse event data. They will also author safety management plans and ensure all activities comply with regulatory requirements and internal SOPs.
The Clinical Data Associate II performs data cleaning, query review, and database quality assessments to ensure the integrity of clinical trial data. They also conduct user acceptance testing on EDC systems and manage study documentation for the Trial Master File.
The Manager will lead clinical data management teams and oversee study portfolios to ensure high-quality project execution and budget adherence. They will also serve as a key escalation point for stakeholders and drive departmental process improvements.
The Clinical Data Manager oversees data management activities across complex global studies from start-up through database lock. They are responsible for ensuring data integrity, managing vendor reconciliation, and driving process improvements to meet project timelines and quality standards.
The specialist will lead the end-to-end planning and execution of U.S. Open Enrollment programs and manage benefits integration for acquisitions and divestitures. They will also serve as a subject matter expert, collaborating with cross-functional teams to ensure accurate administration and employee support.
The Senior CRA is responsible for managing clinical research activities at investigative sites, including site selection, initiation, monitoring, and closeout. They ensure protocol adherence, regulatory compliance, and high-quality data collection throughout the clinical trial lifecycle.
The Manager will lead and develop a team of Clinical Database Programmers to ensure the efficient and accurate delivery of EDC solutions. They will oversee database configuration, validation, and maintenance while partnering with stakeholders to drive operational excellence.
The Specialist will lead the preparation, negotiation, and execution of clinical site agreements while ensuring compliance with regulatory and contractual requirements. They will collaborate with sponsors, legal teams, and clinical sites to manage budgets and resolve contractual risks throughout the study startup process.
The Medical Director provides medical oversight and serves as a Medical Monitor for clinical research studies to ensure participant safety and high-quality execution. They collaborate with cross-functional teams to support protocol development, safety reviews, and strategic client interactions.
Lead data management activities across complex global clinical trials from study start-up through database lock. Coordinate resources and collaborate with cross-functional teams to ensure high-quality data delivery within timelines and budget.
The Associate General Counsel will provide strategic legal guidance on complex regulatory, commercial, and compliance matters across a global clinical research environment. They will lead key legal subject-matter areas, oversee complex sponsor-facing agreements, and mentor legal professionals to drive operational excellence.
The Associate Director will provide strategic Quality Assurance oversight across clinical research programs to ensure regulatory compliance and quality excellence. They will partner with operational teams to identify quality risks, manage CAPAs, and facilitate inspection readiness.
Lead cross-functional project teams to deliver Phase I-IV clinical trials from start-up through closeout while managing project timelines, quality, and budgets. Serve as the primary client contact and drive collaboration across internal stakeholders, external partners, and vendors.
Develop AI-powered tools to automate financial close activities, variance commentary, and financial planning processes. Partner with finance stakeholders to build governed, data-driven solutions that improve financial analysis and decision-making efficiency.
The CRA II is responsible for ensuring the quality, integrity, and success of clinical research studies through site monitoring and management. They will conduct site visits, verify data accuracy, and ensure compliance with study protocols and regulatory standards.
The Senior Specialist will lead the preparation, negotiation, and finalization of clinical trial agreements and investigator budgets. They will also act as a subject matter expert, resolving negotiation issues and collaborating with internal and external stakeholders to ensure process accuracy.
The role involves acting as a subject matter expert to prepare, negotiate, and finalize clinical trial site contracts and budgets. You will also collaborate with internal and external stakeholders to resolve negotiation issues and ensure compliance with regulatory requirements.
The Director of Project Management provides functional leadership and oversight for large, multi-national clinical projects while managing project teams and resources. They are responsible for ensuring project deliverables meet cost, time, and quality standards while maintaining strong client relationships and driving process improvements.
The Grants Payments Data Analyst will develop and maintain forecasting models to support clinical site payments and ensure accurate financial insights. They will collaborate with cross-functional teams to analyze enrollment data, manage budget variances, and ensure compliance with revenue recognition standards.
You will lead global recruitment strategies and manage a team of recruiting professionals to meet evolving business needs. Additionally, you will partner with HR and business leaders to drive proactive hiring solutions and enhance the overall candidate experience.
The Director will develop and implement an enterprise-wide resource optimization strategy to improve workforce productivity, operational efficiency, and financial performance. They will lead cross-functional initiatives, manage financial models for labor efficiency, and drive the adoption of scalable methodologies across the organization.
The Senior Director will oversee the successful conduct of assigned clinical projects and manage personnel recruitment, training, and performance. They are also responsible for developing business strategies, maintaining client relationships, and managing alliance partnerships.
The Regulatory Affairs Specialist will plan, compile, and submit regulatory documentation while ensuring compliance with evolving regulations and ICH GCP standards. They will also act as a key contact for regulatory authorities and provide strategic advice to project teams regarding legislative requirements.
The Senior Security Engineer will own and mature Microsoft and Azure security capabilities, including identity, endpoint, cloud, and network environments. They will partner with internal teams to engineer security services, develop detection and automation, and maintain security baselines.
The Senior Clinical Research Associate is responsible for site qualification, initiation, monitoring, and close-out visits in accordance with GCP and regulatory standards. They also act as a Lead CRA for global studies, coordinating monitoring activities and ensuring data quality and site compliance.
Develop patient- and site-focused insights and support strategies for clinical studies, identifying participation barriers and addressing recruitment, retention, and site needs. Partner with internal teams, clients, advocacy groups, and vendors to incorporate patient perspectives into study planning, operational delivery, regulatory initiatives, and performance measurement.
Coordinate regulatory submissions, site start-up, activation, and maintenance for assigned studies in Mexico, serving as the country-level contact for sites and internal teams. Collect and review essential documents, track progress and risks, advise on local regulatory requirements, and communicate status and mitigation plans.
Manage research activities at clinical trial sites throughout the study lifecycle, including site identification, start-up, training, maintenance, and closeout. Conduct study initiation visits and ensure sites follow informed consent, safety reporting, and regulatory requirements, primarily through remote site management.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring regulatory compliance, managing informed consent, and overseeing safety-related event reporting.
The Senior Manager leads enterprise digital adoption and systems enablement strategy across various corporate and clinical platforms. They manage a team of learning advisors to ensure effective system usage through role-based training, performance support, and continuous improvement metrics.
Provide leadership and direction to clinical site management team members from study start through to closure. Serve as the primary point of contact for clinical monitoring and site activities while managing deliverables to meet study budgets.
The manager will oversee regulatory and ethics committee submissions across EMEA, Asia Pacific, and Latin America while ensuring compliance with global standards. They will also support business development activities, mentor junior staff, and provide strategic regulatory guidance for clinical trials.
The Clinical Scientist is responsible for the review, interpretation, and assessment of oncology clinical data, specifically solid tumor data. They collaborate with cross-functional teams to ensure high-quality data, maintain database integrity, and communicate clinical trends to clients and study teams.
The Operations Manager oversees rater selection, certification, training content, and scale acquisition for clinical trials. They ensure all project operations comply with SOPs, ICH/GCP, and regulatory guidelines while managing study timelines and budgets.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring regulatory compliance, managing site contracts and budgets, and conducting study initiation visits.
Provide leadership and direction to clinical site management team members from study start through to closure. Serve as the primary point of contact for clinical monitoring and site activities while managing deliverables to meet study budgets.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and ongoing maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety protocols while conducting study initiation visits.
The Specialist, Site Contracts is responsible for the preparation, negotiation, and finalization of clinical site agreements and associated budgets. They also manage contract amendments, ensure regulatory compliance, and liaise with internal teams, sponsors, and clinical sites.
The In-house Clinical Research Associate II manages site-related tasks, ensures compliance with GCP and SOPs, and supports clinical trial managers and field CRAs. They are responsible for TMF maintenance, EDC query resolution, and providing operational support for clinical trials.
The Clinical Payments Specialist manages end-to-end investigator payments, including setup, deployment, and reconciliation for assigned clinical studies. They act as a liaison between investigative sites and internal teams while ensuring payments align with clinical trial agreements and budgetary forecasts.
The Senior LMS Administrator manages the global Learning Management System, including creating training modules, maintaining assignments, and resolving user queries. They also provide support for audits, maintain system documentation, and mentor team members to ensure consistent system operation.
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team to ensure tasks are completed accurately and on time. Responsibilities include maintaining project documentation, managing system access, and coordinating trial-related communications.
The role involves drafting, reviewing, and negotiating clinical research site contracts and budgets with investigators and sponsors. You will also liaise with legal and regulatory teams to ensure compliance and facilitate the execution of agreements.
The Senior CRA is responsible for site qualification, initiation, monitoring, and close-out visits in accordance with GCP and regulatory standards. They also provide mentoring to less experienced staff, coordinate global study activities, and ensure the quality and timely submission of clinical data.
The Vendor Contracts Manager is responsible for the full life cycle of vendor contracts, including drafting, negotiating, and executing agreements. They also focus on process improvement and risk mitigation to ensure efficient and compliant business operations.
The Clinical Research Associate is responsible for site qualification, initiation, monitoring, and study close-out visits to ensure protocol adherence and data integrity. They also provide guidance to site staff, manage site documentation, and verify source documents for patient safety and compliance.
The Senior Clinical Research Associate is responsible for site qualification, initiation, monitoring, and study close-out visits to ensure protocol adherence. They also provide mentoring to less experienced staff and manage study documentation, including data verification and safety reporting.
The Senior Clinical Trial Manager oversees clinical study site management activities, leading a team of clinical staff to ensure protocol compliance and data quality. They are responsible for monitoring study progress, managing site relationships, and coordinating global monitoring strategies throughout the study lifecycle.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements, informed consent, and safety reporting while managing site activities remotely.
The Senior Specialist is responsible for drafting, reviewing, and negotiating clinical research site contracts and budgets. They also facilitate the signature process and maintain tracking tools to ensure all project-related documentation is accurately managed.
The Senior Clinical Research Associate is responsible for site qualification, initiation, monitoring, and close-out visits in accordance with GCPs and regulatory standards. They also provide mentoring to less experienced staff, manage study deliverables, and ensure the quality and timely submission of clinical data.
The Senior Salesforce Architect serves as the enterprise design authority, owning the technical roadmap and development standards for the Salesforce and Certinia ecosystem. This role leads the integration of AI-driven capabilities and manages a team of administrators and developers to support commercial business outcomes.
The Director leads the evolution of the finance technology stack and data architecture to integrate AI and intelligent automation across global finance functions. They are responsible for managing the multi-year transformation roadmap, overseeing cross-functional projects, and ensuring alignment with business objectives.
The RTSM Specialist manages the implementation and decommissioning of RTSM systems, ensuring deliverables meet client requirements and company standards. They serve as the primary escalation point for project issues and oversee study design, budget, and vendor work orders.
The associate manages the full spectrum of vendor and client invoice processing, including accounts receivable and accounts payable functions. Responsibilities include reconciling accounts, preparing financial reports, ensuring compliance with internal policies, and assisting with audits and tax filings.
The Senior Site Activation Manager oversees site activation project management, including site identification, regulatory document collection, and contract status monitoring. They serve as the primary point of accountability for study start-up activities, ensuring all tasks are completed on time and within budget.
The specialist serves as the primary point of contact for regulatory submissions, site activation, and maintenance activities for assigned clinical projects. They are responsible for planning, tracking essential documents, and ensuring compliance with ICH GCP and local regulatory requirements.
The Organizational Learning Advisor designs, delivers, and maintains global systems training for critical clinical and enterprise technology platforms like Medidata and Certinia. They partner with cross-functional stakeholders to translate complex workflows and compliance requirements into effective role-based learning experiences.
The Organizational Learning Advisor will build and lead the commercial learning and enablement strategy from the ground up to support revenue growth and client satisfaction. This role involves designing curricula, facilitating training, and partnering with commercial leaders to identify capability gaps and drive behavioral transformation.
The Proposal Manager leads the development of high-quality FSP proposals across various functional service lines including Biometrics and Clinical Operations. They are responsible for coordinating internal strategy meetings, managing proposal timelines, and collaborating with Business Development and Finance to ensure accurate pricing and deliverables.
The Associate is responsible for preparing and rendering client invoices, managing pass-through cost reimbursements, and reconciling billing reports. They also assist with expense claim reviews, process gap identification, and support annual corporate audits and tax filings.
The Clinical Scientist is responsible for the review, interpretation, and assessment of clinical data to ensure high-quality reporting and study integrity. They collaborate with cross-functional teams to manage protocol-defined variables, track safety events, and present key findings to clients and medical monitors.
The Executive Director of Project Management oversees the direction of the project management team, including financial performance, resource management, and strategic business acquisition. They are responsible for maintaining effective client relationships, leading sub-therapeutic groups, and ensuring project deliverables meet sponsor expectations.
The Senior Clinical Research Associate manages research activities at sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while overseeing observational and non-interventional studies.
The Clinical Payments Specialist manages end-to-end global investigator payments, including setup, deployment, and reconciliation for assigned studies. They act as a liaison between clinical research teams and sites while ensuring payments align with contract terms and budgets.
The role involves processing, reviewing, and resolving Trial Master File (TMF) documents while ensuring adherence to regulatory standards and industry best practices. You will perform periodic quality control checks and collaborate with project teams to maintain essential clinical research documentation.
The Associate Director will oversee the clinical data management team to ensure compliance with SOPs, project budgets, and quality standards. They are responsible for providing strategic leadership, managing departmental deliverables, and implementing process improvement initiatives.
The Clinical Payments Specialist manages end-to-end investigator payments, including setup, deployment, and reconciliation for assigned studies. They act as a liaison between investigative sites and internal teams while ensuring payments align with clinical trial agreements and budgetary forecasts.
The Senior Statistician manages statistical project support and provides expert consultancy across clinical trial programs. Responsibilities include developing SAS programs, writing statistical analysis plans, and ensuring compliance with regulatory standards.
The Site Activation Specialist tracks regulatory documents and manages communication with clinical research sites to ensure timely study start-up. They also support site identification activities, including the negotiation of agreements and the review of site feasibility questionnaires.
The Principal Biostatistician assists in designing clinical studies, preparing statistical analysis plans, and interpreting data from pharmacokinetic and clinical trials. They also provide scientific leadership, supervise personnel, and collaborate with interdisciplinary teams to ensure high-quality documentation.
The Senior Director of Project Management is responsible for the overall direction and financial performance of the project management team within a therapeutic group. They oversee project plans, manage client relationships, and lead the recruitment and development of personnel.
The Associate Director of Project Management oversees large, multi-national clinical projects and provides functional leadership, training, and mentoring to Project Managers. They are responsible for ensuring project deliverables meet cost, time, and quality requirements while serving as a key liaison for clients and internal stakeholders.
The Salesforce Administrator will lead the ongoing development, configuration, and maintenance of the Salesforce platform to optimize business processes. They will collaborate with cross-functional teams to design, test, and deploy enhancements while ensuring data integrity and providing user support.
The Clinical Research Associate is responsible for site qualification, initiation, monitoring, and close-out visits to ensure protocol adherence and data integrity. They also provide mentorship to site staff and manage study documentation within the Trial Master File.
Provide leadership and direction to the clinical site management team from study start through to closure. Serve as the primary point of contact for clinical monitoring and site activities while managing deliverables to meet study budgets.
The role involves managing safety management plans, reviewing SAE data for accuracy, and performing data entry into safety databases. Additionally, the associate will generate regulatory reports and ensure compliance with safety regulations throughout the clinical drug development lifecycle.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
The Medical Writer II is responsible for preparing and leading the medical writing team on Phase I-IV study documents, including protocols, clinical trial reports, and investigator brochures. They must ensure all documentation meets regulatory, scientific, and ethical standards while coordinating review cycles with sponsors.
Provide leadership and direction to the clinical site management team from study start through to closure. Serve as the primary point of contact for clinical monitoring and site activities while managing deliverables to meet study budgets.
Provide leadership and direction to clinical site management team members from study start through to closure. Serve as the primary point of contact for clinical monitoring and site activities while managing deliverables to meet study budgets.
The Grants Payable Specialist is responsible for processing site and investigator payments while managing accounting functions like reconciliations and month-end closing. They also handle tax reporting, vendor master data maintenance, and address payment-related queries.
The Regulatory Affairs Specialist will plan, compile, and submit regulatory documentation while ensuring compliance with evolving global regulations. They will also act as a key point of contact for regulatory authorities and provide strategic guidance to project teams.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring regulatory compliance, managing informed consent, and overseeing safety-related event reporting throughout the study lifecycle.
Develop, test, and execute SAS programs to produce CDISC SDTM and ADaM datasets, tables, figures, and listings. Serve as a programming project lead for medium complexity studies while ensuring data quality and regulatory standards are met.
The Clinical Trial Manager is responsible for leading clinical study site management activities and coordinating a team of clinical staff within a geographic region. They ensure site qualification, initiation, monitoring, and close-out activities are conducted in compliance with study protocols and standard operating procedures.
The Site Activation Manager is responsible for coordinating and overseeing site identification, essential document collection, and contract status for clinical trials. They ensure all start-up activities are completed on time and within budget while maintaining compliance with GCP and local regulations.
The Project Manager is responsible for the end-to-end coordination and management of clinical trials from startup through closeout. They lead cross-functional teams to ensure project deliverables meet time, quality, and cost expectations while implementing rescue strategies when necessary.
The Project Manager is responsible for the end-to-end coordination and management of clinical trials from startup through closeout. They lead cross-functional teams to ensure project deliverables meet time, quality, and cost expectations while implementing contingency plans as needed.
The Project Manager is responsible for the end-to-end coordination and management of clinical trials from start-up through closeout. They direct the technical, financial, and operational aspects of projects to ensure deliverables meet quality, time, and cost expectations.
The specialist will manage, compile, and submit regulatory documentation while ensuring compliance with ICH GCP and local requirements. They will also act as a liaison for translation reviews and maintain country-specific patient information and labeling.
The Principal Statistician will design clinical trials, write Statistical Analysis Plans, and provide statistical leadership across various therapeutic areas. They will also develop and validate SAS programs for statistical analysis while ensuring compliance with regulatory standards and sponsor requirements.
The Manager, Regulatory Affairs provides expert regulatory guidance throughout the drug development cycle and oversees the compilation and submission of regulatory dossiers. They are also responsible for mentoring junior staff, managing departmental work practices, and ensuring compliance with international regulations.
The Contract Manager is responsible for the full life cycle of sponsor contracts and change orders, including drafting, budget preparation, and negotiation. They collaborate with internal departments such as Legal, Finance, and Operations to ensure compliance and accurate project scope definition.
The role involves processing, reviewing, and maintaining Trial Master File (TMF) documents in accordance with SOPs and regulatory standards. You will perform quality control reviews and collaborate with project teams to ensure document accuracy and compliance.
The Clinical Research Associate is responsible for site qualification, initiation, monitoring, and study close-out visits to ensure protocol adherence and data integrity. They also provide mentoring to less experienced staff and maintain accurate documentation for the Trial Master File.
The Vice President of Corporate Development will lead the company's global inorganic growth strategy, including mergers, acquisitions, and strategic partnerships. They will manage end-to-end deal execution and coordinate cross-functional teams to ensure successful post-merger integration and value creation.
The role involves processing, reviewing, and maintaining essential clinical trial documents in accordance with SOPs and regulatory standards. You will perform quality control reviews and collaborate with project teams to ensure document accuracy and compliance.
The Regulatory Affairs Specialist will plan, compile, and submit regulatory documentation while ensuring compliance with evolving global regulations. They will also act as a key point of contact for regulatory intelligence and provide strategic advice to project teams regarding submission processes.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure regulatory compliance and data integrity while overseeing site performance throughout the study lifecycle.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with informed consent and regulatory requirements.
The CRA is responsible for managing the full lifecycle of study sites, including qualification, initiation, monitoring, and close-out. They ensure protocol adherence, verify source documents for data veracity, and provide guidance to site staff and junior CRAs.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with informed consent and safety reporting requirements.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Independently manage statistical project support and provide expert consultancy for clinical trial designs and analysis plans. Develop and run SAS programs for data reporting while ensuring compliance with regulatory standards like FDA and ICH.
The Medical Director provides medical management and professional support for clinical research projects as a Medical Monitor. Responsibilities include managing clinical trials, processing Serious Adverse Events, and contributing medical input to study protocols and development programs.
Manage research activities at clinical sites, including site identification, start-up, and close-out. Ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up activities, and study maintenance. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
The CRA is responsible for managing the full lifecycle of clinical sites, including qualification, initiation, monitoring, and close-out visits. They ensure protocol adherence, verify source documents for data veracity, and manage site documentation within the Trial Master File.
Manage research activities at clinical sites, including site identification, start-up activities, and study maintenance. Conduct site initiation visits and ensure compliance with regulatory requirements and safety reporting.
Responsible for the full lifecycle of site management, including qualification, initiation, monitoring, and close-out visits. The role involves ensuring protocol adherence, verifying source documents, and mentoring less experienced CRAs.
Manage complex studies or sponsor portfolios by performing RMC Lead activities and providing subject matter expertise on TMF needs. Oversee quality control processes, develop TMF quality management documents, and present KPI trends to project teams and sponsors.
The Oncology Therapeutic Strategy Lead serves as a therapeutic consultant, supporting the Business Development organization and Therapeutic Area Leads. This role involves creating effective delivery strategies for clinical trials and collaborating with various internal teams to achieve new business targets.
Manage research activities at clinical sites, including site identification, start-up, and close-down processes. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-out. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up activities, and regulatory document collection. Conduct study initiation visits and ensure compliance with informed consent and safety reporting throughout the study lifecycle.
The role focuses on sourcing new sales opportunities through inbound lead qualification and outbound prospecting to drive revenue growth. The manager will engage prospects, set appointments for Business Development partners, and manage sales territories using Salesforce.
Manage and track regulatory submissions for clinical trials in Poland, ensuring compliance with EU-CTR and local regulations. Liaise with project teams to provide strategic guidance on documentation, labeling, and patient consent forms.
Manage research activities at clinical sites, including site identification, start-up, and close-out. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including identification, start-up, maintenance, and close-out phases. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Lead the operational strategy and growth objectives for global regulatory affairs, overseeing the delivery of regulatory activities and supporting roles. Drive business development efforts by contributing to proposals, bid defense meetings, and regulatory costing for site activation strategies.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Lead the architecture, engineering, and operational delivery of enterprise Identity and Access Management (IAM) capabilities. Design and implement scalable identity solutions and automate lifecycle processes across a global, regulated environment.
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team. Key duties include maintaining project portals, managing trial master files, and coordinating project-specific training.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Ensure compliance with regulatory requirements, informed consent, and safety reporting through remote and on-site monitoring.
Liaise with colleagues to organize and submit high-quality regulatory submissions on a timely basis. Maintain country-specific patient information, consent forms, and drug labeling to ensure compliance with ICH GCP and local requirements.
The Risk and Central Monitoring Manager coordinates cross-functional risk management and central monitoring activities for clinical trials in accordance with ICH GCP guidelines. They are responsible for developing monitoring strategies, overseeing risk-based quality management activities, and ensuring inspection readiness throughout the study lifecycle.
The Clinical Scientist leads the review and assessment of clinical oncology data to ensure quality, integrity, and regulatory compliance. They collaborate with cross-functional teams to interpret clinical findings, monitor safety events, and support the development of key regulatory deliverables.
The Senior Project Manager is responsible for the end-to-end coordination and management of clinical trials from start-up to closeout. They oversee the technical, financial, and operational aspects of projects to ensure deliverables meet quality, time, and cost expectations.
The Senior Clinical Research Associate is responsible for managing research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while overseeing observational and non-interventional studies.
