Latest regulatory affairs Jobs

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the strategic development of GSK's oncology portfolio.

GSK

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for GSK's oncology portfolio, focusing on hematological malignancies. Key responsibilities include collaborating with multidisciplinary teams, ensuring patient safety, and contributing to regulatory submissions and publications.

GSK

Hybrid Permanent

Global Program Clinical Head (Neuroscience)

As a Global Program Clinical Head, you will lead end-to-end clinical development programs in Neuroscience, driving strategy, execution, and regulatory compliance. You will collaborate with global teams, influence key decisions, and ensure patient-centric clinical trials.

Novartis London, United Kingdom

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

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

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves creating clinical development plans, providing expert input on trial design and execution, and engaging with external stakeholders to drive strategic insights and support regulatory submissions.

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, 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 providing expert input on trial design, regulatory activities, and engaging with external stakeholders to drive strategic insights.

Pfizer US$214,900 – US$358,100 pa

On-site Permanent

Associate Strategy Director (Associate Consultant) - Clinical Development

This role involves shaping AI and digital health strategies to accelerate clinical development within a collaborative, innovation-driven team. You'll work across project design, protocol development, and digital solution implementation, supporting pharmaceutical partners and AstraZeneca R&D. The position emphasizes strategic consulting, technical evaluation of digital tools, and driving value through scalable, patient-centric innovations in clinical trials.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Scientist in Translational Pathology, Oncology

This role involves working in a lab-based GCP environment, supporting translational pathology and biomarker programs. Responsibilities include maintaining quality standards, managing clinical and research specimens, performing laboratory assays, and collaborating with cross-functional teams to ensure laboratory activities align with project needs.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

The Laboratory Technician will support the Immunoassay group by executing experimental work, maintaining the lab, and ensuring high-quality data for clinical trials. The role involves hands-on lab work, preparing reagents, conducting assays, and maintaining compliance with safety and regulatory guidelines.

Moderna

On-site Contract

Senior Project Specialist, Clinical Supplies

This role involves managing end-to-end clinical supply operations for Moderna’s mRNA-based therapies, ensuring investigational products are labeled, packaged, and distributed efficiently and in compliance with regulatory standards. The specialist coordinates with CROs, vendors, and internal teams to maintain supply chain continuity, troubleshoot logistics, and support digital innovation in supply systems, including AI-enabled tools and IRT platforms.

Moderna

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

This role leads the global development of a respiratory medicine from clinical proof of concept through to approval, serving as the strategic and operational leader of a cross-functional matrix team. The VP Medicine Development Leader defines the asset’s vision, drives evidence-based decision-making, and ensures alignment across R&D, manufacturing, regulatory, and commercial functions to deliver differentiated medicines for patients. The position involves shaping development plans, managing budgets, engaging with regulators, and supporting lifecycle strategies while representing the asset to senior leadership and external stakeholders.

GSK Stevenage, United Kingdom US$309,750 – US$516,250 pa

Hybrid Permanent

Small Molecule CMC Leader - Senior Director

Leads Chemistry, Manufacturing and Controls (CMC) strategy and execution for small molecule, biopharm, or cell and gene therapy medicines from late-stage development through commercialisation. Oversees process development, regulatory filings, supply chain, and lifecycle management across global teams and external partners, ensuring readiness for approval and launch. Role involves high-level governance engagement, risk management, and transition to commercial supply.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent