Latest Drug Discovery Jobs

Head of Global Regulatory Affairs and Strategy

This senior leadership role involves defining and optimizing global regulatory strategies for drug development programs, building a regulatory team and systems, and implementing quality, pharmacovigilance, and medical writing frameworks. The role leverages AI to streamline regulatory workflows and ensure rapid global approval of products.

Isomorphic Labs Cambridge, United Kingdom

On-site Permanent

PKPD Modelling Lead, London

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs London, United Kingdom

Director, Clinical Pharmacology

This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs. Responsibilities include designing clinical studies, authoring regulatory documents, and collaborating with cross-functional teams to expedite drug development.

Recursion North Tyneside, NE29 8EP, United Kingdom US$212,900 – US$297,000 pa

Hybrid Permanent

Interested in an ?

This role is not currently available, but the company is collecting resumes for future internships. Recursion is a clinical-stage TechBio company using AI and automation to advance drug discovery and development across various therapeutic areas.

Recursion United Kingdom

Remote Internship Part-time

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for hematological malignancies, collaborating with a multidisciplinary team to ensure patient safety, scientific integrity, and regulatory compliance. This role involves medical monitoring, data review, and strategic partnerships with thought leaders in the oncology field.

GSK United States

Hybrid Permanent

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 end-to-end development of oncology drugs.

GSK

Hybrid Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regulatory leads, partnering on global strategies, leading resource planning, and representing the function in senior interactions and health authority meetings.

AstraZeneca United States

On-site Permanent

Medical Director, Senior Patient Safety Physician

This role involves leading the clinical safety strategy for drug projects and products, ensuring the safety and risk management of AstraZeneca's pharmaceuticals. You will work on evaluating adverse events, communicating safety data, and contributing to regulatory submissions, all while collaborating with a global team of experts.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent Flexible

Head, Global Medical Affairs Oncology

This role involves leading the global medical affairs strategy for oncology, shaping early portfolio decisions, and ensuring evidence plans meet stakeholder needs. Responsibilities include developing medical plans, generating innovative evidence, and building partnerships with healthcare professionals and scientific leaders.

Novartis London, United Kingdom

Hybrid 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

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.

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. 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.

Pfizer United States

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

(Fixed Term) Manufacturing Associate I

The Manufacturing Associate I will operate production equipment for mRNA vaccines, ensuring compliance with cGMP and safety regulations. They will work in a highly technological environment, collaborating with QA teams, troubleshooting issues, and participating in continuous improvement projects.

Moderna

On-site Temporary