Latest Human Resource Consulting Jobs

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to the design and medical governance of studies, and providing medical expertise and support throughout the trial process. The role is crucial in advancing HIV treatments and working closely with internal and external stakeholders to ensure the success of clinical studies.

GSK

On-site Permanent

NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director role involves developing and delivering Non-Interventional Studies (NIS) project plans, managing resources, and collaborating with various functional teams to ensure accurate and aligned project schedules. Key responsibilities include maintaining data quality in Planisware, forecasting costs, and managing risks.

GSK

Hybrid Permanent

Senior Research Investigator, (Biologics Pharmacology), London

As a Senior Research Investigator, you will contribute to the pharmacology and translational biology strategy of novel large molecule therapeutics, leveraging Isomorphic Labs' cutting-edge AI drug design engine. You will design and execute pharmacology plans, lead in vivo and in vitro evaluations, and collaborate with interdisciplinary teams to advance drug discovery projects from early stages to clinical candidates.

Isomorphic Labs London, United Kingdom

On-site Permanent

Computational Drug Designer, London, Lausanne

As a Computational Drug Designer, you will work on cutting-edge drug discovery projects, applying AI and computational chemistry to design novel molecules. You will collaborate with interdisciplinary teams, contribute to scientific proposals, and mentor junior colleagues in a fast-paced, innovative environment.

Isomorphic Labs United Kingdom

Hybrid Permanent

Staff Product Manager, Agentic Systems

As the Staff Product Manager for Agentic Systems, you will define the technical and scientific capabilities for autonomous science, bridging the gap between in silico models and physical automated labs. You will lead hypothesis-driven product development, prioritize high-impact capabilities, and collaborate with cross-functional teams to optimize the drug discovery pipeline.

Recursion United Kingdom

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

Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves designing, building, and deploying production-grade AI systems to support clinical development and operations. Key responsibilities include developing AI/ML models, automating workflows, and creating decision-support tools. The role requires strong expertise in software engineering, machine learning, and cloud deployment, with a focus on practical, scalable solutions.

Pfizer

On-site Permanent

Senior Regulatory Associate

The Senior Regulatory Associate at Pfizer is responsible for managing regulatory activities for assigned products and markets, including new registrations, MA variations, and renewals. They will work closely with cross-functional teams, national regulatory authorities, and above-country hubs to ensure compliance and support clinical development activities.

Pfizer United Kingdom

Hybrid Permanent

Clinical Sciences Project Manager

This role involves developing and refining processes, risk management strategies, and other activities essential to the success of the Global Collaborative Studies Group (CSG) at ViiV Healthcare. You will lead the Request for Proposal study process, manage study-related activities, and work cross-functionally with various teams to ensure timely and compliant delivery of supported studies.

GSK

On-site Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, influencing regulatory outcomes, and driving cross-functional collaboration to embed intelligence into submission processes and templates.

GSK United Kingdom

Hybrid Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, influencing regulatory outcomes, and driving cross-functional collaboration to embed intelligence into submission processes and templates.

GSK

Hybrid Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, driving cross-functional collaboration, and supporting capability building and training.

GSK

Hybrid Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, influencing regulatory outcomes, and driving cross-functional collaboration to embed intelligence into submission content and processes.

GSK

Hybrid Permanent

Senior Manager - CMC RA [Vaccines/Biopharm/Small Molecules] Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, mentoring staff, and engaging with external agencies to ensure compliance and expedite submissions.

GSK Canterbury, United Kingdom

On-site Permanent

Senior Manager - CMC RA [Vaccines/Biopharm/Small Molecules] Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, and mentoring staff. The position requires a strong understanding of regulatory requirements and the ability to communicate complex issues across departments and with external agencies.

GSK

On-site Permanent