The Senior Clinical Trial Manager will lead clinical site management activities and oversee clinical monitoring throughout the full study lifecycle. They will act as a primary sponsor-facing contact to ensure high-quality study execution, budget adherence, and effective cross-functional collaboration.
The Executive Director is responsible for managing Account Directors and representing the company to key accounts to establish long-term partnerships. They must develop sales territories, account plans, and strategies to drive growth while collaborating with internal operations teams.
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 Clinical Trials Associate provides administrative and project tracking support to the clinical project team to ensure tasks are completed accurately and on time. Key duties include maintaining project documentation, managing system access, and performing quality audits on project portals.
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 Litigation & Employment Paralegal will manage employment litigation, e-discovery, and legal holds while supporting global employment law functions. They will also assist with M&A integration, policy implementation, and provide operational support to the People Strategy & Culture organization.
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 ensure data quality, manage site documentation, and provide guidance to less experienced staff.
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 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 Global Organizational Learning & Development Coordinator manages the operational execution of training logistics, including scheduling, learner communications, and attendance tracking. This role serves as a central point of coordination for enterprise learning programs to ensure consistent delivery and a high-quality learner experience.
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.
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.
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.
The Senior Manager leads enterprise learning operations, compliance training governance, and talent enablement strategies to strengthen workforce capability. They partner with cross-functional stakeholders to align learning systems, audit readiness, and performance management practices with enterprise priorities.
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 PRN Data Coordinator ensures accurate transcription of clinical trial source data into Case Report Forms in compliance with Good Clinical Practice guidelines. They also manage study records, track source documents, and report potential issues to the Senior Manager of Study Conduct.
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 reporting throughout the study lifecycle.
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.
The Site Activation Manager serves as the primary point of accountability for study start-up and maintenance activities on assigned projects. They oversee functional groups to ensure site activation tasks are completed on time and within budget while maintaining clear communication with sponsors and project teams.
The Senior Project Manager is responsible for the overall 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 customer expectations for time, quality, and cost.
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 Payments Associate manages administrative tasks, processes payment-related queries, and maintains accurate records within internal systems. They also support study reconciliation and system migration activities by organizing documentation and tracking project progress.
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 Senior Clinical Research Associate is responsible for site qualification, initiation, monitoring, and study close-out visits to ensure clinical programs are executed with quality. They also provide mentoring to less experienced staff and ensure site compliance with protocols and data integrity.
The Senior Clinical Trials Associate provides administrative and project tracking support to the clinical project team to ensure tasks are completed accurately. They are responsible for maintaining project documentation, managing system access, and coordinating meeting minutes.
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 Clinical Trials Associate provides administrative and project tracking support to the clinical project team. They are responsible for maintaining project documentation, managing system access, and ensuring quality control for trial-related tasks.
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 are responsible for ensuring regulatory compliance, managing site contracts and budgets, and conducting study initiation visits.
The Associate Project Manager is responsible for the end-to-end coordination and management of clinical trials from startup through closeout. They ensure project deliverables meet quality, time, and cost expectations while managing resources and serving as a key client contact.
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 maintenance. They ensure compliance with regulatory requirements and safety protocols while conducting study initiation visits.
Lead and enhance global recruitment strategies while coaching and developing a team of recruiters to ensure high performance. Partner with business leaders to provide market insights and manage the full hiring lifecycle for senior and critical positions.
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 Associate Regional Partner will collaborate with People Business Partners to develop and implement regional strategies for employee attraction, engagement, and performance. They will also serve as local experts on employment practices, ensuring compliance and advising leaders on talent management and organizational change.
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 Senior Specialist is responsible for developing, reviewing, and negotiating site agreements and investigator grants for clinical trials. They act as a subject matter expert, ensuring compliance with regulatory requirements and managing the contract lifecycle from drafting to execution.
The Manager of Talent Acquisition leads the global recruitment strategy, overseeing the attraction, sourcing, and selection processes for high-caliber candidates. They manage a team of recruiters, analyze performance metrics, and collaborate with HR business partners to ensure recruitment needs are met effectively.
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 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 ensure all site-related documentation is accurately filed in the Trial Master File.
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 Manager of Clinical Operations Site Management is responsible for overseeing assigned Clinical Research Associates to ensure performance, quality, and effective utilization. They handle recruitment, training, performance appraisals, and act as a point of escalation for project-related issues.
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 Director will partner with the EVP of Global Quality to develop and execute global quality and compliance strategies across clinical research services. They will lead quality transformation initiatives, oversee regulatory inspections, and manage a team of quality leads to ensure operational excellence and inspection readiness.
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 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 oversee the collection of data and safety reporting throughout the study lifecycle.
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 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 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 Clinical Trial Manager is responsible for leading clinical study site management activities and ensuring compliance with study protocols and SOPs across a geographic region. They will oversee site monitoring, manage project deliverables, and provide leadership to clinical staff to ensure high-quality data and timely study execution.
The Clinical Trial Liaison manages strategic relationships with clinical investigators and site staff to ensure successful trial execution and high-quality endpoints. They provide scientific and operational guidance to project teams while proactively managing site performance and protocol compliance.
The Clinical Research Associate is responsible for overseeing clinical trial activities to ensure quality and adherence to protocols. They work collaboratively with global teams to support the mission of improving patient lives through innovative research.
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 Associate eCOA Manager provides project management oversight for eCOA studies, ensuring deliverables meet SOP standards and timelines. They serve as the primary escalation point for study-related issues and manage financial reviews, budget tracking, and vendor coordination.
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 Senior Clinical Trial Liaison manages strategic relationships with clinical investigators and site staff to ensure successful trial execution and quality endpoints. They provide operational guidance to project teams, monitor site performance, and proactively manage issues related to protocol adherence and patient enrollment.
The Senior Clinical Trial Manager provides leadership and direction to clinical site management teams while overseeing regional CTMs and coordinating study activities. They are responsible for developing monitoring strategies, managing budgets, and ensuring compliance with clinical protocols and regulatory requirements.
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 manager oversees and coordinates all business development activities within the Biometrics and Pharmacovigilance department, including bids, proposals, and change orders. They are responsible for triaging proposals, developing budgets, and ensuring consistency in departmental documentation and strategy.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and regulatory compliance. They are responsible for overseeing site performance throughout the study lifecycle and ensuring adherence to safety and protocol requirements.
The Director of Proposals serves as a subject matter expert for Functional Service Provider (FSP) solutions, leading the full-cycle development of complex proposals and budgets. They collaborate with cross-functional teams to define strategy, manage client deliverables, and ensure the successful submission of proposals.
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 global investigator payments, including setup, deployment, and reconciliation of study payment solutions. They act as a liaison between investigative sites and clinical 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 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 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 Clinical Payments Specialist manages end-to-end investigator payments, ensuring alignment with clinical trial agreements and budgets. They act as a primary point of contact for payment-related queries and perform regular reconciliations and financial reporting.
The Clinical Payments Associate manages administrative tasks, processes payment queries, and maintains accurate financial records within clinical trial systems. They also support system migrations and study reconciliation activities by organizing documentation and tracking project progress.
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 RTSM Specialist provides project management oversight for RTSM study lifecycles, ensuring deliverables meet quality standards and timelines. They serve as the primary escalation point for project issues and manage study budgets, vendor work orders, and system design specifications.
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.
Implement, configure, and maintain pricing tools and automated systems to support commercial solutions and modernization initiatives. Collaborate with cross-functional teams to define technical requirements, perform code reviews, and ensure data integrity across pricing platforms.
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 Category Vendor Manager oversees clinical vendor performance to ensure supply security, safety, and compliance with SLAs and quality standards. They manage vendor relationships, monitor performance metrics, and lead continuous improvement initiatives across the organization.
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 Project Manager is responsible for the overall coordination and management of clinical trials from startup through closeout. They lead core project teams and manage technical, financial, and operational aspects to ensure deliverables meet time, quality, and cost expectations.
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.
The Senior Associate will manage complex TMF activities, oversee quality control processes, and ensure compliance with regulatory standards. They will also act as a subject matter expert, collaborating with project teams and sponsors to maintain essential clinical trial records.
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 Medical Director serves as the Global Lead Medical Monitor for clinical trials, providing therapeutic expertise and protocol-specific training to project teams. They also contribute medical input to clinical development programs and support business development activities through proposal generation and sponsor meetings.
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 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 is responsible for managing research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements, manage informed consent processes, and oversee safety-related event reporting.
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 specialist will analyze PSC workflows to identify inefficiencies and implement automation solutions to improve operational performance. They will also translate complex data into actionable insights and KPIs to support leadership decision-making.
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 Senior Clinical Trial Manager oversees clinical study site management activities and leads a team of clinical staff on complex global studies. They are responsible for ensuring site qualification, initiation, monitoring, and close-out activities while maintaining data quality and project timelines.
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 Director will oversee the delivery of clinical projects within cost, time, and quality requirements while providing direct supervision and mentoring to project managers. They will also collaborate with the Business Development team on proposals and contribute to the continuous improvement of business processes.
The Site Identification and Relationship Manager will lead post-award site identification strategies, including feasibility assessments and outreach coordination. They are also responsible for training assigned resources and overseeing Site Activation Specialist support activities.
The Site Identification and Relationship Manager will lead post-award site identification strategies, including feasibility management and outreach coordination. They are also responsible for training assigned resources and overseeing Site Activation Specialist support activities.
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.
The Senior Legal Contract Manager is responsible for independently reviewing, redlining, and negotiating sponsor-facing legal and commercial contracts. They will manage the full contract lifecycle while collaborating with internal stakeholders to ensure alignment on business, legal, and operational requirements.
The Associate will process, review, and resolve Trial Master File (TMF) documents while ensuring compliance with SOPs and industry regulations. They will also provide administrative support to the RMC Lead, including maintaining quality control checklists and tracking study documentation.
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.
Lead the writing, coordination, and presentation of robust proposals for assigned projects. Collaborate with Account Directors and subject matter experts to manage the proposal development process and ensure accurate service offerings.
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.
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.
The Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer time, quality, and cost expectations.
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.
The Senior Project Manager coordinates clinical trials from start-up through closeout, managing technical, financial, and operational aspects. They collaborate with functional leads to ensure all project deliverables meet customer time, quality, and cost expectations.
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.
Accountable for directing multiple clinical projects simultaneously to ensure delivery within cost, time, and quality requirements. Acts as a liaison for business development and collaborates across functional areas to improve business processes.
The Senior Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer expectations for time, quality, and cost.
Oversee operational activities for Clinical Assessment Technologies (CAT) projects, including resource management and vendor oversight. Lead departmental initiatives, manage study deliverables from launch to close-out, and support business development activities.
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 specialist will plan, implement, and monitor the overall study supply chain strategy to maximize efficiency and minimize costs. This includes managing inventories of study drugs and collaborating with project management and vendors to optimize delivery processes.
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 informed consent and safety reporting requirements.
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-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 identification, start-up, maintenance, and close-out phases. 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.
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 Architect serves as the enterprise owner and strategic leader for the Workday Adaptive Planning platform, overseeing the product vision and roadmap. They partner with Finance and HR leadership to design secure, high-performing models and integrations aligned with business strategy.
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 Director of Business Development is responsible for achieving revenue objectives by identifying new business leads and managing client relationships within the clinical research industry. They will lead proposal development, conduct bid defense meetings, and coordinate strategic efforts with internal teams to secure new contracts.
The Senior Director of Business Development is responsible for driving revenue growth by identifying new business opportunities and managing client relationships within the clinical research industry. They lead proposal development, conduct bid defense meetings, and coordinate strategic interactions between sponsors and internal project teams.
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.
The Associate II is responsible for the collection, processing, evaluation, and reporting of Serious Adverse Event data in accordance with regulatory guidelines and SOPs. They also serve as the Lead PV Associate for studies, authoring safety management plans and performing quality control on safety information.
The specialist will track study-specific site regulatory documents, follow up on necessary actions, and support the development and review of country/site-specific informed consent forms. Responsibilities also include maintaining communication with sites for timely start-up activities and collecting/reviewing essential regulatory documents.
