Latest Research Associate Jobs

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, qualifying, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and gel electrophoresis—to support clinical-stage mRNA programs. The scientist will generate high-quality RNA quantitation data in compliance with GCLP standards, collaborate across clinical and laboratory teams, and contribute to regulatory documentation and sample management strategies. The position emphasizes innovation through digital tools and automation within a fast-paced, compliance-driven environment.

Moderna

Hybrid Permanent

Senior Research Associate, Clinical Biomarker Laboratory, Immunoassays

This role involves hands-on development, qualification, and validation of functional immunoassays to support mRNA-based clinical trials. The scientist will generate and analyze high-quality data in a GCP-compliant lab environment, contribute to assay innovation, and ensure regulatory compliance. Collaboration with cross-functional teams and use of digital tools, including AI-enabled platforms, are integral to supporting clinical development objectives.

Moderna

On-site Permanent

Compound Management Inventory Specialist (Contractor)

This role involves managing compound inventory and supporting high-throughput screening by preparing precise compound plates through automated systems. The specialist will maintain organization across multiple storage locations and ensure accurate, efficient fulfillment of experimental requests in a fast-paced, tech-driven drug discovery environment.

Recursion United Kingdom

On-site Contract

Head of Early Discovery

Your work will change lives. Including your own.The impact You'll MakeThe Head of Early Discovery will lead strategic initiatives to accelerate drug discovery by leveraging cutting-edge technologies, data-driven decision-making, and innovative scientific approaches. This role is pivotal in shaping Recursion’s...

Recursion United Kingdom

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

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategies. The position also focuses on methodological innovation and mentoring colleagues to build statistical capabilities.

GSK

Hybrid Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for oncology clinical programs, working closely with cross-functional teams to design robust clinical trials and drive methodological innovation. You will mentor colleagues and contribute to regulatory strategy, using advanced statistical methods and simulations to inform trial design and risk assessment.

GSK

Hybrid Permanent

Associate Director, Translational Medicine Expert, TM Clinical Pharmacology

This role involves leading and managing multiple First-in-Human and Clinical Pharmacology studies, ensuring medical and scientific excellence. You will provide expert input into study design, safety, and reporting, and collaborate with cross-functional teams to align on program objectives and optimize processes.

Novartis London, United Kingdom

On-site Permanent

Clinical Quality Assurance - Program Lead (Associate Director)

The Associate Director, Clinical Quality Assurance (QA) will lead quality oversight for clinical trials, ensuring compliance with health authority requirements and patient safety. Responsibilities include implementing quality strategies, monitoring risk management, and supporting governance for quality incidents. The role involves collaboration with key stakeholders and active participation in continuous improvement initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, data review, and safety assessments. The Medical Director will also contribute to protocol design, site selection, and investigator training, while mentoring others and ensuring data integrity and quality.

Pfizer United States

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. The position also involves mentoring others and contributing to strategic discussions with key stakeholders.

Pfizer

On-site Permanent

Director – Process Design and Optimisation in Chemical Development

This role involves leading a team in the design and optimisation of chemical processes for drug development. Responsibilities include technical direction, project delivery, regulatory submissions, and mentoring scientists. The position leverages innovative technologies and AI to enhance process efficiency and ensure robust commercial processes.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Business Insights Manager or Secondment)

The Business Insights Manager will analyze data from various sources, including sales and market activity, to develop actionable recommendations that support AstraZeneca’s strategic goals. Key responsibilities include leading market research projects, forecasting, and collaborating with teams in Marketing, Finance, and Market Access, specifically focusing on the Cardio-Renal therapy area.

AstraZeneca London, United Kingdom

Hybrid Contract

Inside Sales Specialist

Nuclera is a venture-backed biotech company headquartered in Cambridge, UK with significant operations in Boston, USA. Our company is the pioneer in bringing rapid protein access to the benchtop. We make proteins accessible through the eProtein Discovery™ System. Through our...

Nuclera Cambridge, United Kingdom

Hybrid Permanent