Latest Research Scientist Jobs

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities to advance GSK’s oncology portfolio. Key responsibilities include developing and executing phase 1-3 clinical trials, collaborating with cross-functional teams, and engaging with key external experts to ensure the successful development and regulatory approval of innovative oncology treatments.

GSK United States

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

Technical Program Coordinator, DDMR, London

As a Technical Program Coordinator, you will support the Drug Design and Medical Research (DDMR) function by managing program planning, monitoring timelines, tracking actions, and reporting risks. You will work closely with drug design teams, internal stakeholders, and external partners to ensure effective communication and alignment across the organization.

Isomorphic Labs London, United Kingdom

On-site Permanent

Director of Engineering (ML Platform), London

This role involves leading the strategic direction and operational excellence of the Platform teams, which enable the training and serving of large-scale AI models in biotech. Responsibilities include defining the long-term vision, mentoring a diverse team, and ensuring robust, scalable, and developer-friendly services across multiple disciplines.

Isomorphic Labs London, United Kingdom

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, safety data review, and clinical data management. The Medical Director will also contribute to protocol design, site selection, and investigator training, while mentoring others and ensuring data integrity and quality.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, data review, and safety assessments. The Medical Director will also contribute to protocol design, site selection, and investigator training, while mentoring others and ensuring data integrity and quality.

Pfizer United States

On-site Permanent

Director, Evidence Generation

This role involves leading the scientific oversight of global evidence generation studies, from Phase IIIb/IV trials to real-world evidence programmes. You will develop and implement integrated evidence strategies, influence product medical strategy, and engage with global stakeholders, including key opinion leaders and patient organisations.

Novartis London, United Kingdom

Hybrid Permanent

Associate Director, Translational Medicine Expert, TM Clinical Pharmacology

This role involves leading and managing multiple First-in-Human and Clinical Pharmacology studies, ensuring medical and scientific excellence. You will provide expert input into study design, safety, and reporting, and collaborate with cross-functional teams to align on program objectives and optimize processes.

Novartis London, United Kingdom

On-site Permanent

(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

Senior Manager - Engineering & Maintenance

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

Software Engineer

This role involves leading the development of Owkin’s Data Transformation Agent (DTA) and contributing to the core components of the platform. You will design and maintain complex data transformation workflows, manage deployments, and collaborate with internal stakeholders to ensure high standards in code and technical practices.

Owkin United Kingdom

Remote Permanent

Executive Medical Director

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus London, W12 7RH, United Kingdom

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, and representing the function in senior interactions and health authority meetings.

AstraZeneca Canterbury, United Kingdom

On-site 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 mentoring regulatory professionals, partnering with directors on global strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Director, Portfolio Development Process & Standards Lead

This role leads the establishment and maintenance of processes and standards across CSL's global Portfolio Development function, ensuring high-quality clinical trial planning, evaluation, and reporting. The Director will drive process improvement, SOP governance, training curriculum development, and cross-functional change initiatives within a dynamic biotech R&D environment. They will work closely with leadership and international teams to reduce complexity, improve quality and speed, and align procedural frameworks across clinical development, biomarkers, and commercial operations.

CSL

Hybrid Permanent