Latest Recruitment Jobs

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-impact, complex global trials in hepatology, renal, and cardiovascular disease, with a focus on late-phase outcomes studies and rare diseases. The position involves shaping operational strategy, managing CRO partnerships, and driving innovation in trial design while ensuring quality and compliance. Leadership includes direct management of clinical teams and strategic input into asset development across the R&D pipeline.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for complex, high-impact assets in hepatology, renal, and cardiovascular disease, with responsibility for global Phase III trials, rare disease programmes, and co-development partnerships. The position involves setting operational strategy, managing CROs and vendors, driving data-led decision-making, and ensuring trial delivery to time, cost, and quality. It also includes direct leadership of clinical operations teams and integration of innovative trial methodologies.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Senior Process Engineer

The Senior Process Engineer role at AstraZeneca involves developing and scaling up sustainable drug substance manufacturing processes. Responsibilities include introducing new equipment, optimizing processes, and collaborating with cross-functional teams to ensure robust and efficient production for clinical and preclinical trials.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Senior Scientist, Translational PKPD

As a Senior Scientist in Translational PKPD Modeling & DMPK, you will apply your expertise in PKPD modeling and simulation to advance cancer biology understanding and accelerate drug discovery. You will provide specialist modeling input into pre-clinical projects, develop PKPD models, predict human dosing, and contribute to early clinical trials. This role involves cross-functional collaboration, strategic decision-making, and enhancing AstraZeneca’s translational research through publications and presentations.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and collaborating with cross-functional teams to ensure compliance with US, EU, and ROW regulations.

Recursion United Kingdom £176,400 – £228,250 pa

Hybrid Permanent Flexible

Head of DMPK

The Head of DMPK will lead the DMPK strategy, ensuring scientific excellence and robust human dose projections. You will collaborate with data science and ML teams to refine predictive ADME models, support external partnerships, and develop a high-performing team.

Recursion United Kingdom US$284,900 – US$400,950 pa

Hybrid Permanent

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leveraging medical platforms, and aligning medical affairs processes across the EU and International regions. Key responsibilities include supporting transversal business prioritization, improving communication with local operating companies, and assisting with data generation processes and real-world evidence studies.

GSK

On-site Permanent

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leading the implementation of Medical Affairs processes, and supporting transversal business prioritization. You will work closely with Local Operating Companies to ensure effective communication, conduct impact assessments, and support data generation processes, including Investigator-Sponsored Studies and Real World Evidence initiatives.

GSK

On-site Permanent

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leading the implementation of Medical Affairs processes, and supporting data generation across the EU and International regions. You will collaborate with local operating companies, conduct impact assessments, and serve as a subject matter expert in innovative processes.

GSK

On-site Permanent

VIDRU Business Programs Strategy Director

The VIDRU Business Programs Strategy Director role involves translating the vision and priorities of the Vaccines and Infectious Diseases Research Unit into coherent, enterprise-wide programs. Key responsibilities include strategic planning, cross-functional collaboration, and ensuring the delivery of measurable business value through data-driven insights and effective governance.

GSK United States

Hybrid Permanent

VIDRU Business Programs Strategy Director

The VIDRU Business Programs Strategy Director role involves translating the vision and priorities of the Vaccines and Infectious Diseases Research Unit into coherent, enterprise-wide programs. Key responsibilities include strategic planning, cross-functional collaboration, data-driven decision-making, and leading matrix teams to deliver measurable business value and support GSK's goals for innovation, trust, and performance.

GSK

Hybrid Permanent

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

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

This role involves planning and executing real-world evidence studies to support the launch and market positioning of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure the generation of high-quality evidence that meets regulatory and payer requirements, driving successful patient access and commercial outcomes.

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 launch and commercial success 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 market requirements.

GSK

On-site Permanent