Latest Managed Services Jobs

Quality Validation and CSV Manager

The Quality Validation and CSV Manager will lead a team responsible for ensuring all validation activities, including process, cleaning, facility, and computer systems validation, comply with regulatory requirements and GSK quality standards. The role involves managing validation protocols, collaborating with cross-functional teams, and providing technical expertise and training.

GSK Barnard Castle, United Kingdom

On-site Permanent

Change Communications Manager – 2 year secondment

Develops and executes internal communications strategies to support organizational change and strategic priorities at a global biopharma company. Works closely with senior leaders to craft messaging, drive employee engagement, and manage change through compelling content and data-driven insights. Focuses on building confidence during transformation using storytelling, AI, and cross-functional collaboration.

GSK United Kingdom

Hybrid Contract

Head of Data & BI Platform Engineering

Leads Pfizer's enterprise data and BI platform engineering, overseeing critical data infrastructure including data warehouses, lakehouses, ETL pipelines, and BI tools. Responsible for platform strategy, reliability, governance, and enabling AI/analytics workflows through scalable, secure, and well-governed data services. Works closely with federated teams to drive adoption, performance, and cost efficiency across a modern data stack.

Pfizer US$274,000 – US$456,600 pa

Hybrid Permanent

Vice President, Strategy, Value & Innovation

Role purposeThe VP, Strategy, Value & Innovation drives what International Commercial’s Digital & AI capacity works on, why it matters, and how value is realized. The role owns the portfolio system, investment logic framework, go/no-go gates, benefits ledger, external innovation...

Pfizer United Kingdom

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, leading quality issue resolution, and ensuring inspection readiness across global clinical programs. The manager will translate regulatory requirements into actionable insights, conduct self-assessments, and drive continuous improvement in compliance. Embedded within cross-functional teams, the role emphasizes proactive risk mitigation, data integrity, and collaboration with Quality Assurance and Development functions.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Clinical Data Strategy, Manager

This role involves designing and executing data strategy plans for clinical trials within Novartis' Translational Medicine portfolio, with a focus on early data planning, risk assessment, and alignment of data collection with scientific objectives. The position supports trial design and data oversight, particularly in the Neuroscience Therapeutic Area, and ensures high-quality, consistent data to enable rapid, data-driven decision-making across global teams.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

Medical Director, Patient Safety Physician

This role involves leading the clinical safety strategy for drug projects and products, evaluating safety data, and managing risk to patients. You will work closely with regulatory agencies, contribute to global submissions, and ensure the safety and efficacy of AstraZeneca's products throughout their lifecycle.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent

Medical Director, Senior Patient Safety Physician

This role involves leading clinical safety strategy for drug projects across development and post-marketing phases, with a focus on oncology. The Medical Director will evaluate safety data from clinical and pre-clinical sources, contribute to global regulatory submissions, and guide risk management using advanced methodologies like signal detection and Safety Knowledge Groups. Based in Luton with a hybrid working model, the position drives patient safety within a global, science-led environment.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent Flexible

Senior Project Specialist, Clinical Supplies

This role involves managing clinical supply operations for Moderna’s mRNA-based therapies, ensuring investigational products are labeled, packaged, and distributed efficiently to clinical sites. The specialist will coordinate with vendors, CROs, and internal teams to maintain supply chain compliance and continuity, while supporting digital innovation and process improvements in clinical supply workflows.

Moderna Oxford, United Kingdom

Hybrid Permanent