Latest Clinical Research Associate Jobs

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, qualifying, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RT-qPCR—to support clinical pharmacokinetic and pharmacodynamic studies within a GCLp-compliant environment. The scientist will work closely with cross-functional teams to ensure robust data generation, maintain regulatory compliance, and integrate emerging digital and automation technologies into workflows. A strong focus on reagent management, assay documentation, and continuous process improvement is central to the position.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, optimizing, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RNA isolation—to support mRNA-based clinical programs. The scientist will work within GCL0-compliant (GCLP) frameworks to generate pharmacokinetic and pharmacodynamic data, ensuring regulatory compliance and data integrity. Collaboration with cross-functional teams and adoption of digital tools and automation are key to advancing clinical trial execution and analytical processes.

Moderna

Hybrid Permanent

Associate Director of Clinical Sciences

Lead clinical sciences strategy and execution for global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. Focus on immuno-oncology with strong emphasis on regulatory compliance, patient safety, and scientific leadership across clinical development phases. Work within a matrix environment to guide study design, interpretation, and regulatory submissions.

GSK Stevenage, United Kingdom

Associate Director of Clinical Sciences

This role involves leading clinical sciences activities in global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. The individual will shape study design, interpret results, and ensure regulatory compliance across phases of development, with a focus on immuno-oncology. The position requires scientific leadership, engagement with external experts, and contribution to regulatory submissions and clinical strategy.

GSK United States

Clinical Data Strategy, Manager

This role involves leading clinical data strategy planning and execution across Translational Medicine programs, with a focus on designing fit-for-purpose data collection approaches and supporting robust decision-making. The individual will develop Data Strategy Plans, guide trial teams on data oversight, and leverage internal and external data to inform trial design—particularly in Neuroscience. The position requires deep expertise in clinical assessments, data integrity, and cross-functional collaboration in a global, fast-paced environment.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

Clinical Development Director - Renal

The Clinical Development Director leads and supports clinical development activities within a global program, focusing on strategy, trial execution, data analysis, and regulatory documentation. This role involves close collaboration with cross-functional teams, ensuring scientific rigor and data quality across phases I–IV trials, particularly in late-phase development. The position requires strong scientific expertise, leadership in clinical operations, and active participation in safety and regulatory initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

Leads clinical development for assigned assets in Internal Medicine, serving as the primary clinical accountability point within Pfizer's Research & Development. Designs and oversees global clinical trials, regulatory submissions, and cross-functional team coordination, with potential involvement in obesity-related late-stage programs. Engages with external stakeholders and ensures compliance with scientific, regulatory, and safety standards.

Pfizer England

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapies. The Global Development Lead will design and oversee global clinical trials, create development plans, and ensure regulatory compliance across regions including China and Japan. The position requires cross-functional leadership, engagement with external stakeholders, and contribution to regulatory submissions and product labeling.

Pfizer England £214,900 – £358,100 pa

On-site Permanent

Director, Portfolio Development Process & Standards Lead

Lead the development and governance of processes, standards, and SOPs for CSL's global Portfolio Development function, ensuring high-quality clinical program execution. Drive cross-functional process improvement initiatives, change management, and training curriculum development. Collaborate with leadership and stakeholders across R&D to streamline decision-making and enhance operational excellence in a dynamic biotech environment.

CSL US$250,000 – US$280,000 pa

Hybrid Permanent

Associate Principal Scientist - In Vivo Pharmacology

Lead and direct in vivo pharmacology studies within multidisciplinary teams to advance preclinical drug discovery programmes targeting kidney diseases such as CKD, AKI, and diabetic nephropathy. Design and interpret translational studies using disease models, support target validation, and guide therapeutic development through biomarker and efficacy analysis. Collaborate with biotech and pharma partners while mentoring scientists and shaping scientific strategy.

Proclinical Nottingham, Nottinghamshire, United Kingdom £50,000 – £500,000 pa

Associate Director, Safety Epidemiology – Global Patient Safety

Lead the design and execution of post-authorisation safety studies using real-world data to assess and communicate the safety profiles of AstraZeneca’s medicines. Provide strategic epidemiological input to regulatory submissions, safety signal evaluations, and diversity initiatives, collaborating with internal teams and external partners. Drive methodological excellence in pharmacoepidemiology and contribute to global patient safety decision-making across a broad product portfolio.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Radiopharmaceutical QP

CMDO is Seeking to Appoint a Qualified Person. The Organisation is Engaged in Developing and Manufacturing New Medicines and Novel Formulations, Including a Wide Range of Oral Solid and Liquid Dosage Forms, Sterilised and Aseptically Filled Products, as well as...

CV-Library City of Westminster, Greater London

Bank Biomedical Scientist

Bank Biomedical Scientist/Spire Manchester / 0 HoursSpire Manchester Hospital has an exciting opportunity for a Biomedical Scientist to join the team on a Bank 0-hour contract.Duties and responsibilities:To assist in the organisation, management and development of services within specialty of...

Spire Healthcare Manchester, United Kingdom

Senior Alliance Manager, London

This role involves managing strategic partnerships in a cutting-edge AI-driven drug discovery environment, ensuring scientific and commercial success. The Senior Alliance Manager will oversee alliance governance, drive collaboration frameworks, and support high-impact partnerships from research to development. A key focus is fostering strong relationships between internal teams and external partners while advancing best practices in alliance management.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Director of Clinical Pharmacology, Cambridge, MA

Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.

Isomorphic Labs Cambridge, United Kingdom