Latest Clinical Research Associate Jobs

Director, Translational Science Lead

This role leads translational science strategy across renal, inflammation, fibrosis, and neurodegeneration disease areas, focusing on biomarker development and validation to support clinical decision-making from preclinical through to launch. The position drives innovation in human translation using advanced technologies and multi-omics data, while providing strategic input across drug development and business development opportunities.

GSK US$178,200 – US$297,000 pa

Hybrid Permanent

Director, Translational Science Lead

Leads translational science strategy across renal, inflammation, fibrosis, and neurodegeneration disease areas, driving biomarker development and validation from preclinical to clinical stages. Integrates multi-omics, human tissue data, and novel technologies to inform drug development decisions and support clinical trial design. Works cross-functionally to align translational insights with research, clinical, and regulatory teams.

GSK US$178,200 – US$297,000 pa

Hybrid Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, including investigators, regulatory bodies, and safety review teams.

Pfizer

On-site Permanent

Oncology Medical Head, International

This role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global and regional teams to ensure patient-centered, evidence-driven medical impact. The position requires deep oncology expertise and leadership to drive strategic decisions, data interpretation, and communication across international markets.

Pfizer United States

On-site Permanent

Senior Director, Epidemiologist

This role involves leading global epidemiology strategy for oncology programs across the drug development lifecycle, with a focus on generating real-world evidence and informing benefit-risk decisions. The Senior Director will represent epidemiology in regulatory discussions, mentor junior staff, and drive innovation in safety science methodologies. Work is conducted in a hybrid or remote setup depending on location.

Novartis London, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.

Novartis Ireland

Hybrid Permanent

Director, Statistical Programming

This role involves leading and developing a team of programmers, providing strategic direction for statistical programming in clinical development, and ensuring quality, compliance, and continuous improvement. The Director will partner cross-functionally to drive business impact and maintain industry and regulatory knowledge.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Biologics Account Manager

This role involves driving adoption of respiratory biologics within secondary care settings by building strategic relationships with multi-disciplinary teams and key healthcare stakeholders. The Account Manager will lead formulary access, support homecare utilization, and execute account plans in a complex clinical environment. It requires strong commercial acumen, deep understanding of the NHS ecosystem, and the ability to navigate multi-stakeholder decision-making units.

AstraZeneca Sheffield, United Kingdom

On-site Permanent

Senior Manager, Planning and Production Solutions—Label Operations

This role involves leading label design, production, and system operations for clinical trial supplies within a GMP and regulatory-compliant environment. The Senior Manager ensures accurate and timely delivery of packaging and labeling solutions using enterprise systems like PRISYM360 and EMD365, while driving process improvements and digital innovation. Collaboration with internal teams and external vendors is key to supporting global clinical studies and advancing supply chain traceability and efficiency.

Pfizer Sandwich, United Kingdom

Hybrid Permanent

Investigator Contracts Lead, Sr. Manager

Leads clinical trial site contract negotiations and budget management for global studies, overseeing agreements and amendments with investigator sites. Acts as a key point of contact for complex contracting strategies, collaborates with legal and finance teams, and mentors junior negotiators. Focuses on risk mitigation, timeline adherence, and process improvements in a remote, matrixed environment.

Pfizer London, SW7 2AP, United Kingdom

Remote Permanent

Investigator Contracts Lead, Sr. Manager

This role leads the negotiation and execution of clinical trial contracts with investigator sites globally, managing both contractual terms and site budgets. The Senior Manager oversees complex or high-priority studies, resolves escalations, and collaborates with Legal, Finance, and pCRO partners to ensure timely site activation. It involves shaping contracting strategies, mentoring junior staff, and driving process improvements in a remote, global environment.

Pfizer Poland

Remote Permanent

Senior Director Translational Data Sciences

This role involves developing and executing a translational data strategy that bridges the gap between disease biology and clinical outcomes. The Senior Director will lead a team in integrating multi-omics data with AI-driven analytics, forming strategic partnerships, and ensuring clinical relevance in all analytical platforms.

GSK Stevenage, United Kingdom

On-site Permanent

Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents, leading cross-functional teams, and managing complex writing projects. The Principal Medical Writer will interpret clinical and statistical data, ensure compliance with regulatory requirements, and contribute to global regulatory submissions.

GSK Stevenage, United Kingdom

Hybrid Permanent

Senior Director Translational Data Sciences

This role involves developing and executing a translational data strategy that bridges the gap between disease biology and clinical outcomes. The Senior Director will lead a team in integrating multi-omics data with AI-driven analytics, forming strategic partnerships, and ensuring clinical relevance in all analytical platforms.

GSK

On-site Permanent

Senior Director Translational Data Sciences

This role involves developing and executing a translational data strategy that bridges the gap between disease biology and clinical outcomes. The Senior Director will lead a team in integrating multi-omics data with AI-driven analytics, collaborate with R&D and clinical development, and establish high-value partnerships with external organizations.

GSK

On-site Permanent