Latest Clinical Research Associate Jobs

Director, Digital Medicine: Respiratory, Immunology & Inflammation Research Unit

This role involves leading the development and implementation of digital medicine strategies to support clinical programs and studies in respiratory, immunology, and inflammation. You will work across various teams to design and validate digital biomarkers, enhance clinical trials with AI, and collaborate with external partners to accelerate capability and delivery.

GSK London, United Kingdom

On-site Permanent

Director, Digital Medicine: Respiratory, Immunology & Inflammation Research Unit

This role involves leading the development and implementation of digital medicine strategies to support clinical programs and studies in respiratory, immunology, and inflammation. The Director will guide cross-functional teams in designing and validating digital biomarkers, collaborating with external partners, and enhancing the efficiency and patient-centricity of GSK's clinical trials.

GSK

On-site Permanent

Oncology Medical Head, International

This senior leadership role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, ensuring patient-centered, evidence-driven decisions and high-quality medical execution across regions. The role requires deep oncology expertise, strategic thinking, and collaboration with global and regional stakeholders to drive the oncology scientific narrative and data interpretation.

Pfizer

On-site Permanent

Oncology Medical Head, International

This senior leadership role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, ensuring patient-centered, evidence-driven decisions, and leading interactions with clinical and research experts. The role requires deep oncology expertise and strong leadership to drive medical impact globally.

Pfizer

On-site Permanent

Statistician (Scientist)

The role involves providing statistical support for manufacturing and analytical processes, using advanced data analytics and visualisation techniques. You will work across multiple teams to improve process understanding and drive data-driven decision-making, contributing to AstraZeneca's digital transformation.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Director, Process Engineering & Packaging

Leads process engineering and packaging for biologics at AstraZeneca, driving development of clinical and commercial drug product processes including fill/finish, device assembly, and packaging. Manages a team of scientists and engineers, oversees technology transfer across internal and external manufacturing sites, and advances design for manufacturability and regulatory strategies. Focuses on innovation, scale-up, and technical excellence within a global biopharmaceutical manufacturing network.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Head, Global Medical Affairs Oncology

This role involves leading the global medical affairs strategy for oncology, shaping early portfolio decisions, and ensuring evidence plans meet stakeholder needs. Responsibilities include developing medical plans, generating innovative evidence, and building partnerships with healthcare professionals and scientific leaders.

Novartis London, United Kingdom

Hybrid Permanent

Virtual Analytics Network (VAN) PhD Graduate Program

This PhD Graduate Program at Novartis involves 15 months of rotations across three key areas of the organization, focusing on clinical trials and statistical analysis. After the rotations, you will choose a permanent role as a Principal Biostatistician, responsible for statistical work on assigned trials and implementing innovative trial designs.

Novartis London, United Kingdom

Hybrid Permanent

Manager, Global Regulatory Strategy, Oncology

This role involves developing and delivering robust regulatory strategies for drug development and approval, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation within the regulatory framework.

GSK United Kingdom

Hybrid Permanent

Manager, Global Regulatory Strategy, Oncology

This role involves developing and delivering robust regulatory strategies for oncology products, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation in regulatory affairs.

GSK

Hybrid Permanent

Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and clear communication. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory compliance and process improvement.

GSK United States

On-site Permanent

Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and compliance. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory submissions and process improvements.

GSK

On-site Permanent

Director, DP Workstream Leader – Small Molecule Parenteral (LAIs and Oligos)

Leads drug product development for sterile long-acting injectables and oligonucleotides, guiding cross-functional teams in formulation, process development, and technology transfer. Ensures robust CMC strategies, regulatory compliance, and supply readiness across clinical to commercial phases. Focuses on delivering high-quality, patient-centric medicines through scientific leadership and matrix collaboration.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Director, DP Workstream Leader – Small Molecule Parenteral (LAIs and Oligos)

Leads late-stage drug product development for sterile long-acting injectables and oligonucleotides, guiding cross-functional teams in formulation, process development, and technology transfer. Translates CMC and regulatory strategies into actionable plans, ensuring robust control strategies and compliance across clinical and commercial phases. Works within a matrix environment to align R&D, manufacturing, and supply chain functions for successful asset delivery.

GSK Stevenage, United Kingdom

Hybrid Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, influencing regulatory outcomes, and driving cross-functional collaboration to embed intelligence into submission processes and templates.

GSK United Kingdom

Hybrid Permanent