Latest Outsourcing Jobs

Associate Director, Biostatistics

The role involves leading statistical strategy and execution across clinical development programs, including study design, data analysis, and regulatory submissions. The individual will provide expert statistical input, manage internal or outsourced programming teams, and represent biostatistics in interactions with global regulatory agencies. Emphasis is placed on innovation, cross-functional collaboration, and delivery of high-quality statistical outputs for clinical trials and submissions.

CSL

Hybrid Permanent

Associate Director, Biostatistics

This role leads the statistical strategy and execution for clinical development programs within a therapeutic area, ensuring robust study design, data analysis, and regulatory compliance. The Associate Director collaborates with cross-functional teams, represents biostatistics in regulatory interactions, and oversees internal or outsourced programming efforts. They also drive innovation in statistical methodologies and contribute to clinical trial interpretation and reporting.

CSL

Hybrid Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

This role leads clinical operations strategy and delivery for GSK's Hepatology, Renal, and Cardiovascular disease portfolio, overseeing end-to-end development from early phase through post-marketing. The leader will manage a matrix team, drive operational excellence, embed data-driven decision-making, and align with enterprise goals to ensure high-quality, efficient clinical delivery across global programs.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Leads clinical operations strategy and delivery for GSK's Hepatology, Renal, and Cardiovascular disease portfolio, overseeing end-to-end development from early phase through phase IV. Responsible for shaping operational direction, managing cross-functional teams, driving data-led decision-making, and ensuring alignment with enterprise goals. Focuses on innovation, risk management, and talent development within a global R&D environment.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Vendor Start-Up Manager - eCOA & Translations

The Vendor Start-Up Manager for eCOA and Translations ensures vendors are aligned and ready to deliver, protecting study timelines, quality, and patient experience. Key responsibilities include technical expertise, risk assessment, continuous improvement, and vendor oversight.

Novartis

Hybrid Permanent

Trial Vendor Associate Director

This role involves managing all clinical vendor-related aspects of global clinical trials, including vendor service delivery, contract negotiations, cost control, and user-acceptance testing for eCOA and IRT systems. You will collaborate closely with the study team and ensure vendor service excellence throughout the trial lifecycle.

Novartis United Kingdom

Remote Permanent

Connectivity Specialist

Evolve are partnering with a driven medical device manufacturer who are seeking a Connectivity Specialist to help shape the future of connected healthcare. This is an exciting opportunity to combine technical expertise, customer engagement, and project leadership to deliver innovative...

Evolve Selection Watford, Hertfordshire, United Kingdom

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for global R&D trials, translating protocols into operational supply strategies, and ensuring on-time delivery of investigational products. The Clinical Trial Supply Manager acts as the key link between clinical teams and supply operations, overseeing demand planning, depot management, and compliance across Phase I–IV studies, including investigator-sponsored and compassionate use trials.

GSK Stevenage, United Kingdom €48,375 – €116,000 pa

On-site Permanent

Director, Oncology Translational Medicine Project Manager

This role leads the planning and execution of translational medicine strategies for GSK's antibody-drug conjugate (ADC) oncology portfolio. The Director drives cross-functional coordination across biomarkers, diagnostics, and clinical development, ensuring integrated project plans, governance readiness, and operational excellence. They provide strategic project management leadership, risk oversight, and insight-driven reporting to support R&D decision-making across the global oncology pipeline.

GSK Stevenage, United Kingdom

Hybrid Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK’s global R&D studies, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The manager will coordinate across depots, logistics partners, and clinical teams to maintain supply continuity, minimise waste, and support study milestones across phases I–IV. It requires strong planning, risk management, and GxP compliance in a patient-focused, global trial environment.

GSK Belgium €69,600 – €116,000 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the clinical trial supply chain for GSK's global R&D studies, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The manager coordinates across depots, logistics partners, and internal teams to maintain compliance, minimise waste, and support study milestones across all phases of clinical development.

GSK €48,375 – €116,000 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK's global R&D trials, translating protocols into supply strategies, and ensuring timely delivery of investigational products. The manager will lead supply planning, coordinate with depots and logistics partners, and act as the primary link between clinical teams and supply operations across Phase I–IV studies. Emphasis is placed on risk-adjusted, patient-focused planning and continuous improvement in compliance with GxP and regulatory standards.

GSK £48,375 – £116,000 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK's global R&D trials, from protocol review to study close-out. The Clinical Trial Supply Manager ensures timely, compliant delivery of investigational products by translating protocols into supply strategies, managing inventory and distribution, and acting as the key link between clinical teams and supply operations across Phase I–IV studies.

GSK €48,375 – €80,625 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for global trials from protocol review to study close-out, ensuring timely delivery of investigational products while minimizing waste. The Clinical Trial Supply Manager acts as the key link between supply chain and clinical teams, developing risk-adjusted supply strategies, overseeing depot operations, and ensuring compliance with GxP and regulatory standards across Phase I–IV studies.

GSK €48,375 – €116,000 pa

On-site Permanent

Director, Oncology Translational Medicine Project Manager

This role leads project management for GSK’s antibody-drug conjugate (ADC) translational medicine programs, integrating biomarker and diagnostic strategies across clinical development. The Director ensures cross-functional coordination, governance readiness, and operational execution across internal teams and external partners, driving strategic planning and compliance for key oncology R&D milestones.

GSK United States

Hybrid Permanent