Latest Pharmaceuticals Jobs

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Head of RTSM (Randomization and Trial Supply Management)

This role involves leading the RTSM function, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, ensuring on-time randomization and supply availability, and improving RTSM processes and governance.

GSK Stevenage, United Kingdom

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes specialized monitoring, regulatory support, and engaging with external stakeholders to drive strategic insights.

Pfizer United States

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of internal medicine assets, working with cross-functional teams to design and execute clinical trials. Key responsibilities include creating clinical development plans, ensuring regulatory compliance, and collaborating with external partners to advance Pfizer's clinical programs.

Pfizer

On-site Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for oncology clinical programs, working closely with cross-functional teams to design robust clinical trials and drive methodological innovation. You will mentor colleagues and contribute to regulatory strategy, using advanced statistical methods and simulations to inform trial design and risk assessment.

GSK

Hybrid Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategy. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK

Hybrid Permanent

Research Pipeline Project Manager

The Research Pipeline Project Manager will lead and coordinate cross-functional pre-clinical research projects, partnering with scientists and clinical teams to advance scientific priorities. Responsibilities include end-to-end planning, risk management, and driving improvements in project delivery processes, with a focus on patient impact and team collaboration.

GSK

Hybrid Permanent

Principal Programmer / Analyst

This role involves leading programming activities for complex clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, while fostering quality assurance and innovation.

GSK

Hybrid Permanent

Principal Medical Writer

The Principal Medical Writer will author and deliver high-quality clinical regulatory documents, lead cross-functional teams in developing clinical dossier documents for global regulatory submissions, and manage complex writing projects. They will interpret complex clinical and statistical information, ensuring compliance with GSK standards and regulatory requirements.

GSK

Hybrid 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. Key responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the quality strategy and risk management.

GSK United Kingdom

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