Latest Managed Services Jobs

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Senior Manager - CMC Regulatory Affairs Biopharm 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

Head of Data & BI Platform Engineering

Leads Pfizer's enterprise data and BI platform engineering, overseeing critical data warehousing, integration, and visualization systems that underpin AI and analytics initiatives. Responsible for strategy, platform reliability, cost governance, and cross-functional collaboration to ensure scalable, secure, and governed data infrastructure. Manages a team of engineers and drives adoption of modern data platforms across a federated organization.

Pfizer US$274,000 – US$456,600 pa

Hybrid Permanent

Head of Data & BI Platform Engineering

Leads the strategy and operation of Pfizer's enterprise data and BI platforms, including data warehousing, integration, and visualization tools. Ensures reliable, governed, and high-performing platforms that support AI and analytics workloads across the organization. Focuses on SLA-driven service delivery, cost optimization, and cross-functional collaboration to enable data-driven decision-making.

Pfizer US$274,000 – US$456,600 pa

Hybrid Permanent

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, and ensuring adherence to quality standards across global clinical programs. The manager will lead investigations into quality issues, drive inspection readiness, and translate regulatory requirements into practical actions. Collaboration with cross-functional stakeholders is central to strengthening compliance and fostering a culture of data integrity and accountability.

Novartis London, United Kingdom

Hybrid Permanent

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 Study Administrator

As a Clinical Study Administrator, you will coordinate and manage the administrative aspects of clinical trials, ensuring that all documentation, regulatory submissions, and stakeholder communications are accurate and timely. You will work closely with various teams to maintain inspection readiness and support the smooth operation of multi-site studies.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Regulatory Transparency (Disclosures) Professional

In this role, you will manage the end-to-end execution of clinical trial registration and results posting, ensuring Roche complies with global regulations. You will lead the accurate and timely posting of clinical trial data, manage cross-functional teams, and ensure consistency and quality in all submissions.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent

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

Executive Assistant, London

This role involves providing high-impact administrative and operational support to senior leadership, managing complex calendars, coordinating cross-functional initiatives, and ensuring seamless logistics across global time zones. The Executive Assistant will act as a trusted partner, enabling leaders to focus on strategic priorities through proactive problem-solving and meticulous coordination. The position operates at the intersection of efficiency, confidentiality, and innovation within a fast-paced AI-driven drug discovery environment.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Supply Planner

The Supply Planner ensures uninterrupted production by managing raw material procurement and inventory across clinical and commercial manufacturing operations. This role involves running MRP processes, maintaining inventory policies, coordinating with suppliers and 3PLs, and leading supply continuity efforts. The position works cross-functionally with finance, quality, and manufacturing teams to align supply plans with demand forecasts and resolve supply chain disruptions.

Autolus Stevenage, United Kingdom

Hybrid Permanent

Regulatory Science Professional - Intelligence

This role involves managing regulatory intelligence for Roche’s pharmaceutical and medical device portfolio in the EU, with a focus on generating strategic, data-driven insights. The professional will leverage AI tools, maintain regulatory databases, and collaborate across global teams to inform decision-making and drive innovation in a dynamic regulatory environment.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Director, Process Engineering & Packaging

Leads process engineering and packaging for biologics at AstraZeneca, driving development of clinical and commercial drug product processes including fill/finish, device assembly, and packaging. Manages a team of scientists and engineers, oversees technology transfer across internal and external manufacturing sites, and advances design for manufacturability and regulatory strategies. Focuses on innovation, scale-up, and technical excellence within a global biopharmaceutical manufacturing network.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Reward and People Analytics Partner, London

This role focuses on ensuring data integrity and operational efficiency within People systems, with responsibilities spanning data management, tool administration, compensation cycle support, and reporting. The individual will leverage AI and automation to streamline workflows, deliver insights on reward metrics, and enhance how the People team operates at scale. It's a data-driven position that bridges technical analysis with human resources operations in a high-impact AI-driven research environment.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Vice President, Head of Strategy & Operations

Your work will change lives. Including your own.The Impact You'll MakeRecursion is reimagining drug discovery through the integration of automated cell biology, high-dimensional data, and AI-driven analytics. As Head of Strategy & Operations, you will be our CEO's closest strategic...

Recursion North Tyneside, NE29 8EP, United Kingdom