Latest Research Associate Jobs

Associate Director, Regulatory Affairs

This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent

(Fixed-Term) Manufacturing Associate II - Shift Position

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization...

Moderna Oxford, United Kingdom

Associate Director, Clinical Operations, Pricing and Analytics

The Role:Reporting to the Director, Business Analytics & Operations Management, the Associate Director, Business Analytics & Insights, Clinical Operations will be accountable for development and implementation of analytical & financial systems & tools and processes to perform business analytics within...

Moderna

Associate Director, Operations Excellence Supported Studies

This role leads operational excellence for Supported Studies at GSK, focusing on data governance, system ownership, and digital integration. The individual will ensure data integrity, drive compliance with regulatory requirements like Transfer of Value, and translate operational needs into scalable digital solutions. Working across cross-functional teams, they will enhance efficiency, quality, and transparency in clinical operations through robust dashboards, automation, and process improvements.

GSK Stevenage, United Kingdom US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and digital foundations of GSK's Supported Studies, ensuring data integrity, system performance, and compliance. The individual will lead data governance, dashboard development, and system integration—particularly for platforms like Veeva and IdeaPoint—while acting as a bridge between business and technology teams to drive efficiency and compliance in clinical study delivery.

GSK London, United Kingdom US$154,275 – US$257,125 pa

Hybrid Permanent

Clinical Development Medical Director (Associate Director)

The Clinical Development Medical Director (Associate Director) oversees medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and clinical support for studies, with potential mentorship and strategic input.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to the study team and external stakeholders.

Pfizer

On-site Permanent

Senior Clinical Development Medical Director - Renal

The Senior Clinical Development Medical Director will lead the strategy and execution of renal clinical development programs, from early to late phases. Responsibilities include providing clinical leadership, developing regulatory documents, ensuring patient safety, and collaborating with global teams and stakeholders.

Novartis London, United Kingdom

On-site Permanent

Senior Clinical Development Medical Director - Renal

The Senior Clinical Development Medical Director will lead the strategy and execution of renal clinical development programs, from early to late phases. Responsibilities include providing clinical leadership, developing regulatory documents, ensuring patient safety, and collaborating with global teams and stakeholders.

Novartis

On-site Permanent

Senior Director, Project Operating Model and Leadership Excellence

This position will lead the transformation of project leadership capabilities across the R&D enterprise. On a systemic level, this role will prepare critical GPL roles (Exec Directors) to be CEO of the project via a bespoke leadership/drug development/executive training and...

CSL

Director, Portfolio Development Process & Standards Lead

This role leads the establishment and maintenance of processes and standards across CSL's global Portfolio Development function, ensuring high-quality clinical trial planning, evaluation, and reporting. The Director will drive process improvement, SOP governance, training curriculum development, and cross-functional change initiatives within a dynamic biotech R&D environment. They will work closely with leadership and international teams to reduce complexity, improve quality and speed, and align procedural frameworks across clinical development, biomarkers, and commercial operations.

CSL

Hybrid Permanent

Biomedical Scientist

Biomedical Scientist | Pathology | Full Time | Perm | ManchesterWe're looking for a motivated Biomedical Scientist to join our Pathology team at Manchester Hospital. This full‑time, role offers the chance to work in a supportive, well‑equipped laboratory while playing...

Spire Healthcare Manchester, United Kingdom

PhD Level Ultrasound Technology Consultant - Cambridge

This role involves advancing surgical and interventional medical technologies through the application of deep ultrasound expertise. You'll lead high-impact technical programmes from feasibility to market readiness, working on intelligent instruments and robotic surgical systems. Collaboration with multidisciplinary teams and external partners is central, with a focus on solving complex scientific challenges and translating innovations into real-world clinical applications.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Software Engineer

This role involves leading the development of Owkin’s Data Transformation Agent (DTA) and contributing to the core components of the platform. You will design and maintain complex data transformation workflows, manage deployments, and collaborate with internal stakeholders to ensure high standards in code and technical practices.

Owkin United Kingdom

Remote Permanent

Principal Clinical Project Manager

This role leads complex or pivotal clinical trials from conception to closeout, overseeing cross-functional teams and vendor partnerships. The Principal Clinical Project Manager ensures study delivery within quality, timeline, and budget targets, applying risk-based quality management and driving inspection readiness. They also mentor junior staff and contribute to process improvements within clinical operations.

Autolus London, W12 7RH, United Kingdom

Hybrid Permanent