Latest Medical Services Jobs

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory approvals and strategic insights.

Pfizer

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This role 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 GDL also provides expert input on trial design, regulatory activities, and external stakeholder engagement.

Pfizer

On-site Permanent

Precision Medicine Director

Job Description Summary#LI-HybridWork Arrangement: Hybrid WorkingNovartis is unable to offer relocation support: please only apply if accessible.The Precision Medicine Director is responsible for developing and executing precision medicine strategies aligned to disease area and clinical program objectives. This role leads...

Novartis

Senior Principal Biostatistician

This role involves leading the implementation of innovative trial designs and statistical models, collaborating with clinical and regulatory teams, and contributing to exploratory analyses and statistical consultations. The position requires a strong background in biostatistics and the ability to drive quantitative decision-making in clinical trials.

Novartis London, United Kingdom

Hybrid Permanent

Production Technician

This role involves hands-on production work in a regulated manufacturing environment, focusing on tasks such as weighing, mixing, packing, and assembly in compliance with GMP standards. The technician will follow SOPs, operate machinery, and maintain accurate batch records. It’s a quality-driven position within a stable, full-time day shift schedule.

RBW Consulting Wimbledon, London, SW19 7NL, United Kingdom

On-site Permanent

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

DOCUMENT CONTROLLER

Compliance and Documentation AdministratorCrewe£28275 per annumFull-Time, PermanentAn excellent opportunity has arisen for an organised and detail-oriented Compliance and Documentation Adminitrator to join a successful and growing organisation operating within a highly regulated industry.This role is ideal for someone with strong...

KPI Recruiting Crewe Green, Cheshire, CW1 5UN, United Kingdom £28,275 pa

Associate Director, Biostatistics 2

The role involves leading the statistical aspects of clinical development programs, including study design, data analysis, and regulatory submissions. Responsibilities include collaborating with cross-functional teams, managing CROs, and representing Biostatistics in regulatory interactions.

Appcast Enterprise Maidenhead, SL6 1QB, United Kingdom

On-site Permanent

Project Quality Lead

This role involves leading quality strategy across the full product lifecycle in a pharmaceutical development environment. You'll drive design reviews, risk management, and quality system implementation while working closely with project teams and stakeholders. The position emphasizes proactive quality integration rather than post-hoc review, with a focus on influencing technical decisions and ensuring compliance through GMP and ISO standards.

Next Phase Recruitment United Kingdom

On-site Contract

Senior Scientist 2 MSAT

This role involves leading the transfer and scale-up of bioprocesses from development into GMP manufacturing environments. The scientist will design and oversee technical studies, ensure regulatory compliance, and support root cause analysis and process robustness. Working closely with cross-functional teams, they will drive successful process implementation in a highly collaborative, multidisciplinary setting.

SRG Darlington, County Durham, United Kingdom

On-site Permanent

Metabolite Identification Specialist

This role involves leading metabolite identification and biotransformation studies to determine the metabolic fate of drug candidates. The specialist will design and interpret advanced analytical data using techniques like high-resolution mass spectrometry, support drug discovery and development programmes, and provide scientific guidance to project teams and junior scientists. The position emphasizes technical leadership, problem-solving in complex metabolic pathways, and direct contribution to the progression of pharmaceutical candidates.

SRG Sandwich, United Kingdom

On-site Permanent

Principal Food Scientist

Lead and design investigative research into how food processing methods affect product functionality, stability, and performance. Apply food chemistry and analytical techniques to generate actionable insights and support innovation across frying, roasting, baking, blending, and mixing processes. Work hands-on in a site-based environment to deliver scientifically robust studies and collaborate with cross-functional teams.

SRG Gloucestershire, United Kingdom

On-site Permanent

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

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regulatory leads, partnering on global strategies, and representing the function in senior interactions and health authority meetings.

AstraZeneca Canterbury, United Kingdom

On-site Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include mentoring regulatory professionals, partnering with directors on global strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent