Latest Medical Devices Jobs

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 Stevenage, United Kingdom

Hybrid Permanent

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

Global Development Lead, Internal Medicine, Sr. Director (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 strategic planning, regulatory submissions, and engagement with external stakeholders to drive the clinical development program.

Pfizer Manchester, M1 4HD, United Kingdom

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 specialized monitoring, regulatory support, and engaging with external stakeholders to drive strategic insights.

Pfizer United States

On-site Permanent

Head of RII or Oncology Programming

This senior leadership role involves overseeing the transformation of clinical data into regulatory-ready evidence for GSK's Respiratory, Immunology & Inflammation (RII) or Oncology Research Unit. The Head of RII or Oncology Programming will lead a global team, drive strategic initiatives, and champion innovation in clinical programming, ensuring high standards of quality, compliance, and timely delivery of medicines and vaccines.

GSK Stevenage, United Kingdom

On-site Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working closely with internal and external teams to ensure studies are delivered on time, on budget, and in compliance with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK Poland

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study conduct, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key documents, coordinating meetings, managing communications, and overseeing clinical supplies and budget tracking.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Clinical Sciences Manager, Global Collaborative Studies – ViiV Healthcare 10 month maternity cover

This role involves leading and managing ViiV Healthcare's supported studies, including investigator-sponsored and collaborative studies. Responsibilities include reviewing study proposals, ensuring compliance with policies, and maintaining strong relationships with external investigators and internal stakeholders.

GSK United Kingdom

On-site Temporary

Clinical Sciences Manager, Global Collaborative Studies – ViiV Healthcare 10 month maternity cover

This role involves leading and managing ViiV Healthcare's supported studies, including investigator-sponsored and collaborative studies. Responsibilities include managing study proposals, ensuring compliance, and building relationships with external investigators and internal stakeholders. The role is crucial for generating evidence to inform HIV treatment and advancing ViiV's mission.

GSK

On-site Temporary

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning, designing, and executing real-world evidence studies to support the commercial success and market positioning of GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and payer requirements.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the commercial success of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure that evidence is aligned with regulatory and payer requirements, and will be responsible for managing timelines, budgets, and deliverables.

GSK

On-site Permanent