Latest Pharmaceutical Scientist Jobs

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology antibody drug conjugate (ADC) portfolio, focusing on advancing the development of clinical trials from early to late stages. Key responsibilities include protocol development, medical monitoring, safety data review, and collaboration with a multi-disciplinary team of experts to ensure the scientific integrity and timely delivery of clinical trials.

GSK

Hybrid 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

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL

Director Biostatistics - Hematology

The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and...

CSL

Executive Director, Strategy, Oncology R&D

This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership on complex strategic topics, optimize investment decisions, and collaborate across functions to deliver impactful patient outcomes.

AstraZeneca

On-site Permanent

Regulatory Affairs Intelligence Director

This role involves translating regulatory intelligence into strategic decisions that accelerate drug development and improve patient outcomes. You will work closely with senior leaders to anticipate regulatory shifts, shape external policy, and convert complex data into actionable insights.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s full clinical portfolio, from early-stage studies to pivotal trials and submission support. The VP will build scalable operating models, manage global trials, and ensure operational excellence in a data-driven, patient-centered, and technology-enabled environment.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent

Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s development portfolio, from study planning to study closeout. You will build and mentor a high-performing team, manage global trials, and ensure operational excellence in an AI-native TechBio company.

Recursion United Kingdom

On-site Permanent

(Fixed-Term) Manufacturing Associate, Drug Substance - Shift Position

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...

Moderna

(Fixed-Term) Manufacturing Associate II - Shift Position

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization...

Moderna

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer will be responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer United Kingdom

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director will lead the development and maintenance of Quality Plans, ensure inspection and audit readiness, and provide quality oversight of process deviations and investigations. This role involves interpreting and applying regulatory requirements, identifying and mitigating compliance gaps, and driving continuous improvement in pan-regulatory processes and data quality.

Pfizer London, SW7 2AP, United Kingdom

On-site Permanent

Mechanical Design Engineer - Pharmaceutical

Position: Mechanical Design EngineerLocation: LiverpoolSalary: Competitive / negotiable dependent on experience (Likely £40k-£50k)Mechanical Design Engineer required for a pharmaceutical manufacturer based in Liverpool. The successful candidate will be designing and developing mechanical engineering aspects of complex machinery to a project...

Bennett & Game Recruitment Halewood, Merseyside, United Kingdom £40,000 – £50,000 pa

QA/ Validation Supervisor, Pharmaceutical

This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, managing QA documentation, participating in audits, and driving continuous improvement initiatives.

NMS Recruit Ltd t/a Russell Taylor Group Worsley, Manchester, M28 2GE, United Kingdom £40,000 – £45,000 pa

On-site Permanent

Validation/ Quality Assurance Specialist, Pharmaceutical

The Validation/Quality Assurance Specialist will plan and execute validation activities, author and maintain validation protocols, and collaborate with cross-functional teams to ensure compliance with GMP standards. The role involves maintaining validated status, supporting regulatory inspections, and contributing to the Site Validation Master Plan.

NMS Recruit Ltd t/a Russell Taylor Group Swadlincote, Derbyshire, DE11 0AG, United Kingdom £30,000 – £34,000 pa

On-site Permanent