Latest IT Recruitment Jobs

Associate Medical Director, Safety Evaluation and Risk Management (SERM)

This role involves leading safety evaluation and risk management for GSK’s clinical and post-marketing assets, providing medical expertise in pharmacovigilance and safety strategy. The Associate Medical Director will lead cross-functional teams, contribute to regulatory submissions, and ensure robust safety governance. It requires strong scientific judgment, leadership in a matrix environment, and a focus on patient safety across global development programs.

GSK Manchester, M4 6AL, United Kingdom €87,000 – €145,000 pa

Hybrid Permanent

Associate Medical Director, Safety Evaluation and Risk Management (SERM)

This role involves leading the safety evaluation and risk management of GSK’s clinical and post-marketing pharmaceutical assets. The Associate Medical Director will provide medical oversight for signal detection, risk assessment, and regulatory reporting, ensuring patient safety is prioritized across global development programs. Working within a cross-functional, matrixed environment, the role shapes safety strategy, influences governance decisions, and contributes to high-impact regulatory submissions.

GSK €87,000 – €145,000 pa

Hybrid Permanent

Associate Medical Director, Safety Evaluation and Risk Management (SERM)

This role involves providing medical and scientific leadership in safety evaluation and risk management for GSK’s clinical and post-marketing assets. The Associate Medical Director will lead signal detection, risk assessment, and pharmacovigilance strategy, working across global cross-functional teams to ensure patient safety and regulatory compliance. Key responsibilities include safety oversight, regulatory reporting, and contributing to clinical development with a focus on evidence-based decision-making and risk mitigation.

GSK €87,000 – €145,000 pa

Hybrid Permanent

SERM Medical Director

The SERM Medical Director role at GSK involves providing in-depth medical and scientific expertise in safety evaluation and risk management for key GSK assets. Responsibilities include leading pharmacovigilance, developing safety strategies, and ensuring compliance with regulatory standards. The role also involves cross-functional team leadership, communication of safety issues, and contributing to the continuous improvement of safety processes.

GSK United Kingdom

On-site Permanent

Clinical Sciences Manager, Global Collaborative Studies – ViiV Healthcare 10 month maternity cover

This role involves leading and managing ViiV Healthcare's supported studies, including investigator-sponsored and collaborative studies. Responsibilities include reviewing study proposals, ensuring compliance with policies, and maintaining strong relationships with external investigators and internal stakeholders.

GSK United Kingdom

On-site Temporary

Clinical Sciences Manager, Global Collaborative Studies – ViiV Healthcare 10 month maternity cover

This role involves leading and managing ViiV Healthcare's supported studies, including investigator-sponsored and collaborative studies. Responsibilities include managing study proposals, ensuring compliance, and building relationships with external investigators and internal stakeholders. The role is crucial for generating evidence to inform HIV treatment and advancing ViiV's mission.

GSK

On-site Temporary

VIDRU Business Programs Strategy Director

The VIDRU Business Programs Strategy Director role involves translating the vision and priorities of the Vaccines and Infectious Diseases Research Unit into coherent, enterprise-wide programs. Key responsibilities include strategic planning, cross-functional collaboration, and ensuring the delivery of measurable business value through data-driven insights and effective governance.

GSK United States

Hybrid Permanent

VIDRU Business Programs Strategy Director

The VIDRU Business Programs Strategy Director role involves translating the vision and priorities of the Vaccines and Infectious Diseases Research Unit into coherent, enterprise-wide programs. Key responsibilities include strategic planning, cross-functional collaboration, data-driven decision-making, and leading matrix teams to deliver measurable business value and support GSK's goals for innovation, trust, and performance.

GSK

Hybrid Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning, designing, and executing real-world evidence studies to support the commercial success and market positioning of GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and payer requirements.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the commercial success of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure that evidence is aligned with regulatory and payer requirements, and will be responsible for managing timelines, budgets, and deliverables.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the launch and market positioning of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure the generation of high-quality evidence that meets regulatory and payer requirements, driving successful patient access and commercial outcomes.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the launch and commercial success of GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and market requirements.

GSK

On-site Permanent

Head of RII or Oncology Programming

This role involves leading the clinical data programming for GSK's Respiratory, Immunology & Inflammation or Oncology Research Unit. Responsibilities include setting high standards for data quality, driving innovation with technologies like Generative AI, and collaborating with cross-functional teams to accelerate the development and submission of new medicines and vaccines.

GSK United Kingdom

On-site Permanent

Head of RII or Oncology Programming

This role involves leading the clinical data programming for GSK's Respiratory, Immunology & Inflammation or Oncology Research Unit. Responsibilities include setting high standards for data quality, driving innovation with technologies like Generative AI, and collaborating with cross-functional teams to accelerate the development and submission of medicines and vaccines.

GSK

On-site Permanent

Head of RII or Oncology Programming

This senior leadership role involves overseeing the transformation of clinical data into regulatory-ready evidence for GSK's Respiratory, Immunology & Inflammation, or Oncology Research Units. The Head of Programming will lead a global team, drive strategic initiatives, and champion innovation in clinical programming, ensuring high standards of quality and compliance.

GSK

On-site Permanent