Latest Healthcare Jobs

Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents, leading cross-functional teams, and managing complex writing projects. The Principal Medical Writer will interpret clinical and statistical data, ensure compliance with regulatory requirements, and contribute to global regulatory submissions.

GSK Stevenage, United Kingdom

Hybrid Permanent

Manager, Global Regulatory Strategy, Oncology

This role involves developing and delivering robust regulatory strategies for drug development and approval, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation within the regulatory framework.

GSK United Kingdom

Hybrid Permanent

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA submissions, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna Poland

On-site Permanent

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA activities, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna

On-site Permanent

Team Lead, Therapeutic Area Quality

The Team Lead, Therapeutic Area Quality, leads a team of Quality Business Partners, ensuring quality is integrated into R&D programs and projects. Responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the global audit plan. The role also involves talent development and maintaining expertise in international regulations.

GSK

On-site Permanent

Team Lead, Therapeutic Area Quality

This role involves leading a team of Quality Business Partners to ensure quality is integrated into R&D programs and projects. Responsibilities include evaluating quality strategies, driving continuous improvements, and supporting health authority inspections. The role also focuses on talent development and maintaining expertise in international regulations.

GSK

On-site Permanent

Team Lead, Therapeutic Area Quality

This role involves leading a team of Quality Business Partners to ensure quality is integrated into R&D programs and projects. Responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the quality strategy and risk management. The role requires a deep understanding of regulatory requirements and the ability to lead a global quality team.

GSK

On-site Permanent

SERM Scientific Director

The SERM Scientific Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. This role involves driving pharmacovigilance activities, evaluating safety data, and collaborating with cross-functional teams to ensure robust benefit-risk profiles and patient safety. The position requires significant experience in pharmacovigilance and a strong understanding of global regulations.

GSK

On-site Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with internal and external teams to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and supplies.

GSK Stevenage, United Kingdom

Hybrid Permanent

Analytical Chemistry - Platform Modalities Leader

This role involves leading the strategic expansion and modernization of analytical chemistry platforms for complex therapeutic modalities, including small molecules, drug conjugates, and oligonucleotides. The Platform Modalities Leader will drive the adoption of new technologies, ensure robust and scalable analytical capabilities, and provide hands-on technical leadership while influencing cross-functional teams.

GSK Stevenage, United Kingdom

On-site Permanent

Director Medical Writing Process Management

The Director Medical Writing Process Management will lead the optimization of end-to-end business processes within Medical Writing, ensuring compliance, efficiency, and continuous improvement. They will collaborate with cross-functional teams to implement best practices, monitor process health, and align with GSK’s strategic goals.

GSK Stevenage, United Kingdom

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 (RII) or Oncology Research Unit. The Head of RII or Oncology Programming will lead a global team, drive strategic initiatives, and champion innovation in clinical programming, ensuring high standards of quality, compliance, and timely delivery of medicines and vaccines.

GSK Stevenage, United Kingdom

On-site Permanent

MSAT Drug Product Lead (Parenteral Products)

This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading New Product Introduction (NPI), technology transfers, process verification, and regulatory submissions. The position requires strong technical expertise, collaboration across functions, and a focus on quality and compliance.

GSK East Hertfordshire, United Kingdom

On-site Permanent

MSAT Drug Product Lead (Parenteral Products)

This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading New Product Introduction (NPI), technology transfers, process verification, and regulatory compliance. The position requires strong technical expertise, collaboration across functions, and a focus on quality and patient safety.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Product Director, Molecule Design Products

The Onyx Research Data Tech organization represents a major investment by GSK R&D and Digital & Tech, designed to deliver a step-change in our ability to leverage data, knowledge, and prediction to find new medicines. We are a full-stack shop...

GSK Stevenage, United Kingdom