Latest regulatory affairs Jobs

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, focusing on advancing the development of antibody drug conjugates (ADCs) for solid tumors. Key responsibilities include collaborating with multidisciplinary teams to design and execute clinical trials, ensuring high-quality protocol development, and engaging with key external experts to drive data generation and regulatory approvals.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the clinical research activities for GSK’s oncology portfolio, including developing and executing phase 1-3 clinical trials. They will collaborate with various stakeholders to ensure high-quality protocol development, medical monitoring, and data interpretation, while also engaging with key external experts and thought leaders.

GSK

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 and executing clinical trials, creating development plans, and ensuring regulatory compliance. The role also includes collaborating with cross-functional teams, providing expert input on clinical data, and engaging with external stakeholders to drive strategic insights.

Pfizer

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 assigned assets in Internal Medicine. This involves designing and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes providing expert input on trial design, regulatory activities, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

Quality Engineer

The Quality Engineer is responsible for developing, implementing, and maintaining quality plans, metrics, processes, and systems to ensure Azenta Life Science products consistently meet the highest standards of reliability, performance, and regulatory compliance.This role serves as a technical quality leader,...

Azenta Life Sciences Partington, Manchester, United Kingdom

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development and strategic oversight of a medicine for cardiovascular and renal conditions. Responsibilities include managing the Clinical Development Team, ensuring high clinical and scientific standards, and authoring key study documents and regulatory submissions.

CSL

On-site Permanent

Senior Systems Engineer, GXP Systems

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna Oxford, United Kingdom

On-site Permanent

Fixed Term Manufacturing Associate II

This role involves operating production equipment for mRNA vaccines, adhering to cGMP and safety regulations, and participating in continuous improvement initiatives. The candidate will work closely with QA, troubleshoot equipment issues, and maintain meticulous documentation in a fast-paced, team-oriented environment.

Moderna

On-site Temporary

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic area opportunities, from Phase 2 through marketed drugs. Responsibilities include engaging with Key Opinion Leaders, driving due diligence, and shaping the portfolio through high-impact partnerships.

CSL United States £263,000 – £328,000 pa

Hybrid Permanent

Director – Process Design and Optimisation in Chemical Development

This role involves leading a team in the design and optimisation of chemical processes for drug development. Responsibilities include technical direction, project delivery, regulatory submissions, and mentoring scientists. The position leverages innovative technologies and AI to enhance process efficiency and ensure robust commercial processes.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Medical Director, Patient Safety Physician

This role involves leading the clinical safety strategy for drug projects and products, evaluating safety data, and managing risk to patients. You will work closely with regulatory agencies, contribute to global submissions, and ensure the safety and efficacy of AstraZeneca's products throughout their lifecycle.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent

Head of DMPK

The Head of DMPK will lead the strategic direction of drug metabolism and pharmacokinetics, ensuring robust scientific excellence and predictive modeling. Key responsibilities include defining DMPK strategies, collaborating with data science teams, and leading a high-performing team.

Recursion London, United Kingdom £166,500 – £208,100 pa

Hybrid Permanent

Head of DMPK

The Head of DMPK will lead the DMPK strategy, ensuring scientific excellence and robust human dose projections. You will collaborate with data science and ML teams to refine predictive ADME models, support external partnerships, and develop a high-performing team.

Recursion United Kingdom

Hybrid Permanent

Field Service Engineer - Stoke-on-Trent to Wrexham

As a Field Service Engineer, you will provide essential technical support for Roche’s medical diagnostic systems, ensuring seamless operation and maximum uptime. Your responsibilities include troubleshooting complex faults, performing preventive maintenance, and delivering technical training to customers. You will work closely with key stakeholders to align service and sales objectives, maintaining rigorous compliance and administrative documentation.

Roche United Kingdom

On-site Permanent

Field Service Engineer - Stoke-on-Trent to Wrexham

As a Field Service Engineer, you will provide essential technical support for Roche’s medical diagnostic systems, ensuring seamless operation and maximum uptime. Your responsibilities include troubleshooting complex electro-mechanical faults, performing preventive maintenance, and training customers to use Roche’s diagnostic systems effectively.

Roche

On-site Permanent