Latest Managed Services Jobs

Study Manager

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

GSK Poland

Hybrid Permanent

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 on time, on budget, and compliant with standards. Key responsibilities include monitoring study conduct, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Head of Data & BI Platform Engineering

Leads Pfizer's enterprise data and BI platform strategy, overseeing critical data warehousing, integration, and visualization systems that serve as the foundation for AI and analytics workloads. Responsible for building and operating scalable, secure, and governed platforms including Snowflake, Databricks, Tableau, and Alteryx, while driving reliability, cost efficiency, and adoption across a federated organization. Manages engineering teams, vendor relationships, and cross-functional collaboration to ensure data platforms deliver trusted, AI-ready data at scale.

Pfizer US$274,000 – US$456,600 pa

Hybrid Permanent

Head of Data & BI Platform Engineering

Leads Pfizer's enterprise data and BI platform engineering, overseeing data warehousing, integration, and visualization platforms critical to AI and analytics. Responsible for strategy, SLA-driven operations, cost governance, and reliability of platforms like Snowflake, Databricks, Tableau, and Alteryx. Partners with AI and data teams to ensure governed, high-quality data access across a federated model.

Pfizer US$274,000 – US$456,600 pa

Hybrid Permanent

Senior Tax Manager – Tax Reporting and UK Tax Compliance

Senior Tax Manager – Tax Reporting and UK Tax ComplianceLocation: Cambridge, London or Luton UKAbout AstraZenecaAstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious...

AstraZeneca Chatham, ME4 4NP, United Kingdom

Health Economics Manager

Job Title: Health Economics ManagerLocation: Pancras Square, LondonCompetitive salary and benefitsAbout the RoleWe are seeking an experienced Health Economics Manager to lead the development and delivery of health economic strategies and evidence that demonstrate the value of innovative therapies and...

AstraZeneca London, United Kingdom

Global Clinical Operations Budget Manager

As a Global Clinical Operations Budget Manager, you will translate complex study assumptions into financial insights, manage budgets and forecasts for clinical trials, and work closely with clinical and finance teams to ensure transparency and accuracy. The role involves partnering across a global matrix environment to drive smarter decisions and optimize trial delivery, ultimately accelerating the development of innovative medicines.

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

Hybrid Permanent

Global Clinical Operations Budget Manager

This role involves managing budgets and financial forecasts for clinical trials, working closely with clinical and finance teams to ensure accuracy and transparency. You will translate complex study assumptions into actionable financial insights, optimize trial delivery, and support process improvements in a global matrix environment.

Novartis London, United Kingdom

Hybrid Permanent

Principal Scientist, TechBio Discovery

Your work will change lives. Including your own.The Impact You'll MakeRecursion is at the forefront of reimagining drug discovery by integrating technological innovations across biology, chemistry, automation, data science, and engineering to radically improve lives by industrializing drug discovery. We...

Recursion United Kingdom £198,000 – £271,700 pa

Hybrid Permanent

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and work closely with manufacturing and quality teams.

Moderna London, United Kingdom

On-site Permanent

Director, CMC Regulatory Affairs

Lead the development and execution of CMC regulatory strategy for small molecule drugs in global clinical trials and marketing applications. Author and manage high-quality regulatory submissions across the US, EU, and rest of world, while advising cross-functional teams on compliance, risk mitigation, and regulatory best practices. Support clinical trial materials and GMP inspections, ensuring alignment with evolving global regulations.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote Permanent

Master Scheduler, Engineering

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus Stevenage, United Kingdom

Medical Device Programme Lead

Balance technical, regulatory and commercial challenges in this fulfilling roleThis highly regraded Cambridge-based medical technologies company is seeking a proven engineering leader to help guide high-value development programmes from concept through to transfer to manufacture. Your leadership will accelerate development...

ECM Selection Cambridge, Cambridgeshire, United Kingdom £75,000 – £95,000 pa

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and contribute to the development of regulatory processes and procedures.

Moderna

On-site Permanent

Product Development Scientist

Right Match Recruitment Group has the privilege to recruit on behalf of our very prestigious client based in Dartford, Kent.We are recruiting for experienced and forward thinkingProduct Development Scientist. This is full time and permanent position and working for very...

Premier Group Recruitment Dartford, United Kingdom £30,000 – £32,000 pa

Permanent