Latest Managed Services Jobs

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

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, 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

Head of Data & BI Platform Engineering

Leads Pfizer's enterprise data and BI platform infrastructure, overseeing critical systems like Snowflake, Databricks, Tableau, and Power BI. Ensures platforms are reliable, scalable, and aligned with AI and analytics needs across the organization. Focuses on governance, performance, cost optimization, and integration with AI-ready data initiatives.

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 critical data infrastructure including data warehouses, ETL pipelines, and BI tools. Ensures platforms are reliable, scalable, and aligned with AI and analytics needs across the organization. Focuses on SLA-driven operations, cost governance, security compliance, and cross-functional collaboration to enable self-service data access.

Pfizer US$274,000 – US$456,600 pa

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

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

This role involves leading the development and submission of regulatory documents, providing strategic direction, and negotiating with health authorities to expedite approvals. The position also focuses on ensuring compliance and timely approval of new and marketed products, serving as a regulatory liaison throughout the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent

Senior Global Clinical Operations Director

This role leads the operational strategy and end-to-end delivery of global clinical programs in oncology, spanning early and late-phase development. The director will drive trial design, cross-functional collaboration, and regulatory readiness while managing complex multinational studies, CRO partnerships, and high-performing teams. Emphasis is placed on innovation, efficiency, and patient impact through advanced trial methodologies and strategic leadership.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Senior Specialist, Data Science

Job Title: Senior Specialist, Data Science — Operational Data Strategy (ODS), BioPharma R&DLocation: United KingdomCompetitive Salary & Excellent Company Benefits!Introduction to the Role:The Operational Data Strategy (ODS) function provides strategic oversight for how clinical operations data is collected, organized, validated,...

AstraZeneca Cambridge, United Kingdom

Director, Regulatory Affairs

This role involves leading global regulatory strategy for drug development programs, managing regulatory submissions across all stages of development, and ensuring compliance with international health authorities. The Director will collaborate with cross-functional teams to identify regulatory risks, guide clinical development, and shape the future of regulatory science using innovative technology-driven approaches in a fast-paced TechBio environment.

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

Remote Permanent

Associate Director, Biostatistics

The role involves leading statistical strategy and execution across clinical development programs, including study design, data analysis, and regulatory submissions. The individual will provide expert statistical input, manage internal or outsourced programming teams, and represent biostatistics in interactions with global regulatory agencies. Emphasis is placed on innovation, cross-functional collaboration, and delivery of high-quality statistical outputs for clinical trials and submissions.

CSL

Hybrid Permanent

Associate Director, Biostatistics

This role leads the statistical strategy and execution for clinical development programs within a therapeutic area, ensuring robust study design, data analysis, and regulatory compliance. The Associate Director collaborates with cross-functional teams, represents biostatistics in regulatory interactions, and oversees internal or outsourced programming efforts. They also drive innovation in statistical methodologies and contribute to clinical trial interpretation and reporting.

CSL

Hybrid Permanent

Senior Project Specialist, Clinical Supplies

This role involves managing end-to-end clinical supply operations for Moderna’s mRNA-based therapies, ensuring investigational products are labeled, packaged, and distributed efficiently and in compliance with regulatory standards. The specialist coordinates with CROs, vendors, and internal teams to maintain supply chain continuity, troubleshoot logistics, and support digital innovation in supply systems, including AI-enabled tools and IRT platforms.

Moderna

Hybrid Permanent

Director, Clinical Pharmacology

This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs, designing clinical studies, and authoring regulatory documents. You will work closely with cross-functional teams to solve drug development challenges and expedite decision-making through modeling and simulation.

Recursion United Kingdom US$212,900 – US$297,000 pa

Hybrid Permanent

Principal/Senior Site Reliability Engineer

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche United Kingdom

Software Engineer (TechOps), London

You will work on a groundbreaking platform that transforms the biopharmaceutical world, partnering with engineers, scientists, and ML researchers to build cloud infrastructure and software foundations. The role involves designing, operating, and refining cloud infrastructure, developing tools, and making core technical decisions in a fast-paced, interdisciplinary team.

Isomorphic Labs United Kingdom

Hybrid Permanent