Latest Innovation Jobs

RTSM Project Manager

The RTSM Project Manager is responsible for the design, development, testing, and maintenance of clinical studies using the RAMOS IRT system. Key responsibilities include ensuring data integrity, configuring complex study designs, and driving continuous improvements in clinical supplies systems. The role involves technical oversight, problem-solving, and collaboration with cross-functional teams to enhance IRT processes and support clinical development.

GSK Stevenage, United Kingdom

Hybrid Permanent

Laboratory Lead Analyst

The Laboratory Lead Analyst role involves supporting the Ware manufacturing site’s laboratories by providing expert analytical services, troubleshooting, and ensuring compliance with GMP and EHS regulations. Responsibilities include overseeing batch testing, verifying data accuracy, and collaborating with cross-functional teams to drive continuous improvement initiatives.

GSK East Hertfordshire, United Kingdom

On-site Permanent

Senior Data Platform Engineer

Your work will change lives. Including your own.Recursion is a leading, clinical-stage TechBio company decoding biology to industrialize drug discovery. Central to its mission is the Recursion Operating System (OS), a platform built across diverse technologies that continuously expands one...

Recursion United Kingdom

Vice President, Real World Evidence (RWE)

Your work will change lives. Including your own.The Impact You’ll Make:Recursion is currently seeking a seasoned leader to join our team as Vice President, Real World Experience. This role will lead RWE generation across the Recursion portfolio. The role will...

Recursion United Kingdom

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves supporting site selection, training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer

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

SERM Medical Director

The SERM Medical Director role at GSK involves providing in-depth medical and scientific expertise in safety evaluation and risk management for key GSK assets. Responsibilities include leading pharmacovigilance, developing safety strategies, and ensuring compliance with regulatory standards. The role also involves cross-functional team leadership, communication of safety issues, and contributing to the continuous improvement of safety processes.

GSK United Kingdom

On-site 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