Latest clinical research associate Jobs

NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director role involves developing and delivering Non-Interventional Studies (NIS) project plans, managing resources, and collaborating with various functional teams to ensure accurate and aligned project schedules. Key responsibilities include maintaining data quality in Planisware, forecasting costs, and managing risks.

GSK

Hybrid Permanent

NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director is responsible for developing and delivering high-quality NIS Project Plans, managing resources, and collaborating with various functional teams to ensure alignment with R&D and marketed product portfolios. The role involves maintaining accurate project schedules, forecasting costs, and ensuring data quality in Planisware.

GSK

Hybrid Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity 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 external committees and site-facing colleagues, to ensure the successful execution of clinical studies.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity 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 supporting site selection, protocol training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer

On-site Permanent

Global Labelling Manager, Content

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels and regulatory guidance, and ensuring compliance with global standards across the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Manager, Content (Neuroscience)

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels, and ensuring compliance with regulatory standards across different markets.

Novartis

Hybrid Permanent

Logistics Coordinator – Temperature-Controlled Supply (5 Month Secondment

This role involves supporting the day-to-day logistics activities for clinical studies, ensuring medicines are delivered on time and under the correct temperature conditions. You will manage temperature excursions, coordinate with logistics partners, and contribute to continuous improvement initiatives.

AstraZeneca Macclesfield, United Kingdom

On-site Contract

Associate Principal AI & ML Engineer – Evinova

As an Associate Principal AI & ML Engineer at Evinova, you will develop and integrate advanced algorithms and generative AI systems to optimize clinical trial design and improve drug development processes. Your role involves working with multi-source data, building production systems, and collaborating with cross-functional teams to drive impactful solutions.

AstraZeneca London, United Kingdom

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 delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

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. Responsibilities include monitoring study progress, drafting key clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

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 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

Programming Leader

The Programming Leader will oversee project-level and study-level programming strategy and delivery for multiple complex studies in GSK's global pipeline. You will collaborate with cross-functional teams, ensure high-quality outputs, and champion agile methodologies and new technologies to enhance programming efficiency and data analysis.

GSK

Hybrid 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