Latest Managed Services Jobs

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and ensuring compliance with ICH/GCP guidelines. The role emphasizes innovation, risk management, and stakeholder communication.

GSK

Hybrid Permanent

Clinical Sciences Project Manager

This role involves managing and refining processes for investigator-sponsored research studies, supporting the Global Collaborative Studies Group in evidence generation, and leading the Request for Proposal study process. The candidate will work cross-functionally with various teams to ensure timely and compliant delivery of studies and contribute to the mission of advancing HIV research and treatment.

GSK United Kingdom

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, ensuring data integrity, and supporting site selection and training.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, ensuring data integrity, and supporting site selection and training.

Pfizer

On-site Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Lead clinical operations strategy for Hepatology, Renal, and Cardiovascular disease portfolios within GSK's R&D engine. Drive end-to-end delivery of global clinical assets, manage high-performing teams, and ensure operational excellence across phases I–IV. Champion data-driven decision-making, inspection readiness, and innovation while aligning with enterprise goals and shaping future development operations.

GSK United Kingdom US$242,550 – US$404,250 pa

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

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to protocol development, and providing medical oversight and support. You will work closely with internal and external stakeholders to ensure the successful execution and interpretation of clinical studies, with a focus on advancing HIV treatments and prevention.

GSK United Kingdom

On-site Permanent

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to the design and medical governance of studies, and providing medical expertise and support throughout the trial process. The role is crucial in advancing HIV treatments and working closely with internal and external stakeholders to ensure the success of clinical studies.

GSK

On-site Permanent

Senior Global Medical Director Oncology

This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing global medical teams, managing external partnerships, and ensuring scientific quality and compliance.

GSK US$241,500 – US$402,500 pa

On-site Permanent

Senior Global Medical Director Oncology

This role involves leading the global medical strategy for a lung cancer asset, working with cross-functional teams to translate scientific insights into practical patient impact. Responsibilities include chairing a global medical team, managing external partnerships, and ensuring scientific quality and compliance.

GSK US$241,500 – US$402,500 pa

Remote Permanent

Clinical Programmer/Analyst

The Clinical Programmer/Analyst designs, builds, and reviews programming solutions to transform clinical and real-world data into reliable results for analysis and reporting. Working closely with statisticians and cross-functional teams, the role involves developing validated datasets, tables, listings, and figures in compliance with regulatory standards such as SDTM, ADaM, and TFL. The position supports agile delivery within a hybrid work environment and emphasizes code quality, regulatory adherence, and innovation in data programming practices.

GSK United Kingdom

Hybrid Permanent

Director, CMC Regulatory Affairs

Leads global CMC regulatory strategy for small molecule medicines, working across R&D, supply, quality, and commercial functions to ensure regulatory compliance and uninterrupted patient supply. Provides strategic direction on regulatory submissions, mentors regulatory staff, and engages with global authorities. Focuses on solving complex regulatory challenges while aligning with business objectives and patient impact.

GSK

Hybrid Permanent

Assistant General Counsel - R&D

Lead legal support for GSK’s R&D discovery and translational platforms, advising on collaborations, data governance, regulatory compliance, and risk management. Partner with scientific and business leaders to enable technology-driven drug discovery and development, draft complex agreements, and provide strategic legal guidance in a global, science-led environment.

GSK United Kingdom

Hybrid Permanent

Assistant General Counsel - R&D

Lead legal support for GSK’s R&D Technologies and Translational Sciences teams, advising on collaborations, data governance, and regulatory compliance in drug discovery and development. Provide strategic legal guidance on academic partnerships, data licensing, and sample management while working cross-functionally to mitigate risks and accelerate R&D. Matrix-manage legal colleagues and contribute to policy responses and training to strengthen legal awareness across science teams.

GSK

Hybrid Permanent