Latest Medical Services Jobs

Senior Director, Global Health Outcomes, ViiV Healthcare

This role involves leading the global health outcomes function at ViiV Healthcare, designing and delivering robust evidence to support HIV treatment and prevention medicines. Responsibilities include strategic leadership, evidence generation, and collaboration with various stakeholders to optimize patient access and value demonstration.

GSK

On-site Permanent

Senior Director Translational Data Sciences

This role involves developing and executing a translational data strategy that bridges the gap between disease biology and clinical outcomes. The Senior Director will lead a team in integrating multi-omics data with AI-driven analytics, forming strategic partnerships, and ensuring clinical relevance in all analytical platforms.

GSK

On-site Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation priorities into portfolio planning. The position requires deep clinical expertise and a proven track record in business development and deal-making.

CSL £263,000 – £328,000 pa

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation into portfolio planning. The position requires deep clinical expertise, a proven track record in deal-making, and strong collaboration with cross-functional teams.

CSL £263,000 – £328,000 pa

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of internal medicine assets, working with cross-functional teams to design and execute clinical trials. Key responsibilities include creating clinical development plans, ensuring regulatory compliance, and collaborating with external partners to advance Pfizer's clinical programs.

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-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 creating clinical development plans, providing expert input on trial design and execution, and engaging with external stakeholders to drive strategic insights and support regulatory submissions.

Pfizer

On-site Permanent

Clinical Trials Associate

The Clinical Trials Associate will manage Trial Master File (TMF) activities, ensuring compliance and inspection readiness. Responsibilities include coordinating documentation, supporting study start-up and close-out, and assisting with site visits and data management.

SRG Hitchin, Hertfordshire, SG5 1HP, United Kingdom

On-site Permanent

Quality Engineer

The Quality Engineer will manage product quality issues, implement corrective actions, and collaborate with cross-functional teams to enhance quality and optimize processes. Key responsibilities include leading problem-solving sessions, monitoring quality metrics, and supporting new product introductions.

Azenta Life Sciences Wotton, Surrey, Surrey, United Kingdom

On-site Permanent

Chemistry Lead (Induced Proximity), London

As a Chemistry Lead in the Induced Proximity team, you will develop and apply a cutting-edge platform to tackle traditionally intractable drug discovery problems. You will collaborate with AI/ML and Drug Design teams to drive projects towards clinical trials, focusing on innovative molecular glue design and synthesis.

Isomorphic Labs United Kingdom

Hybrid Permanent

Senior Clinical Application Specialist - MCS

This role involves driving the adoption of advanced clinical applications in microsurgery and tumour workflows, working closely with surgeons, clinical teams, and hospital decision-makers. The Specialist will support technology integration, engage key stakeholders, and contribute to strategic business development and revenue growth.

Manpower Manchester, United Kingdom

Hybrid Permanent

Mechanical Engineer

Mechanical Engineer | Bristol (Hybrid)We're working with a global engineering leader in the semiconductor manufacturing equipment sector to find a Mechanical Engineer to support the delivery of complex, high-tech systems used across advanced global manufacturing processes.This is a strong opportunity...

Roc Search Europe Limited Bristol, Bristol (county), United Kingdom

DMPK Lead, London

As a DMPK Lead, you will drive the DMPK strategy for drug discovery projects, integrating quantitative pharmacology and AI-first approaches. You will design and implement DMPK strategies, optimize the use of datasets, and collaborate with interdisciplinary teams to advance drug design and development.

Isomorphic Labs United Kingdom

Hybrid Permanent

Field Sales Representative - Self Employed

This role involves placing photo biomodulation devices into retail locations across Central London. Responsibilities include researching target locations, booking meetings, and providing initial training to staff. The role is about building face-to-face relationships and ensuring successful free trial placements.

Amplifying Life Old Street, London, United Kingdom £1,000 – £12,000 pd

On-site Contract

Associate Director, Safety Epidemiology – Global Patient Safety

This role involves leading the design, execution, and reporting of post-authorisation safety studies using real-world data. The candidate will collaborate with various teams to produce high-quality evidence for regulatory decisions and risk management, ensuring AstraZeneca's medicines are safe and effective.

AstraZeneca Chatham, ME4 4NP, 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