Latest Pharmaceutical Scientist Jobs

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leveraging medical platforms, and aligning medical affairs processes across the EU and International regions. Key responsibilities include supporting transversal business prioritization, improving communication with local operating companies, and assisting with data generation processes and real-world evidence studies.

GSK

On-site Permanent

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leading the implementation of Medical Affairs processes, and supporting transversal business prioritization. You will work closely with Local Operating Companies to ensure effective communication, conduct impact assessments, and support data generation processes, including Investigator-Sponsored Studies and Real World Evidence initiatives.

GSK

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (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 approvals and global market access. The role also includes specialized monitoring, regulatory submissions, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine, working closely with cross-functional teams to design, execute, and interpret clinical studies. Key responsibilities include creating clinical development plans, regulatory submissions, and providing expert input on trial design and execution, while ensuring compliance and strategic insight generation.

Pfizer

On-site Permanent

Risk Surveillance Lead

The Risk Surveillance Lead drives the adoption of RBQM practices in clinical trials, overseeing risk assessment, documentation, and continuous improvement. They work closely with cross-functional teams to ensure quality risk management and compliance with regulatory standards.

Novartis London, United Kingdom

Hybrid Permanent

Principal Statistical Programmer

The Principal Statistical Programmer leads statistical programming activities for large or pivotal clinical studies, ensuring high-quality and timely deliverables. They collaborate with cross-functional teams, mentor other programmers, and maintain compliance with industry standards.

Novartis London, United Kingdom

On-site Permanent

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

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 United Kingdom

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 strategies. The position also focuses on methodological innovation and mentoring colleagues to build statistical capabilities.

GSK

Hybrid Permanent

Commercial Head, Lung Europe

This role involves defining and leading the European commercial strategy for GSK’s lung oncology portfolio, ensuring alignment with global strategies and driving successful product launches across multiple European markets. Key responsibilities include performance management, cross-functional collaboration, and ensuring patient access to GSK medicines.

GSK

On-site Permanent

Regional EM Engineering Lead

This role involves ensuring strong engineering performance at Contract Manufacturing Organization (CMO) sites, focusing on Large Molecule Drug Substance. Responsibilities include site assessments, capital project management, and engineering support for new product introductions and existing GSK products.

GSK United States

On-site Permanent

Regional EM Engineering Lead

This role involves ensuring strong engineering performance at Contract Manufacturing Organization (CMO) sites, supporting new product introductions, and managing engineering programs for Large Molecule Drug Substance. The position requires expertise in engineering aspects of large molecule drug substance and involves site assessments, capital management, and troubleshooting.

GSK

On-site Permanent

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

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

GSK Irvine, Alba / Scotland, KA12 8EL, United Kingdom

Hybrid Permanent

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

Hybrid Permanent

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

Hybrid Permanent