Latest Clinical Research Associate Jobs

Medical Director, Oncology Clinical Development - Hematology

This role involves providing medical leadership in oncology clinical development, with responsibilities spanning study design, medical monitoring, safety oversight, and data interpretation. The Medical Director will integrate physician-level insights into clinical trials, collaborate with cross-functional teams and external experts, and contribute to regulatory submissions and scientific communications. The position emphasizes patient-centered decision-making and real-world impact in cancer treatment innovation.

GSK £222,750 – £371,250 pa

Hybrid Permanent

Executive Director, Respiratory

Leads translational biology strategy in respiratory diseases, integrating human-relevant model systems and multi-omics data to drive target validation and clinical translation. Builds and leads a team across internal and external research, with focus on inflammatory and fibrotic lung conditions including COPD, IPF, and ILD. Partners cross-functionally to shape portfolio strategy and advance biomarker development.

GSK Stevenage, United Kingdom

Hybrid Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves developing and maintaining global labelling strategies and core documentation for pharmaceutical products in the cardiovascular, renal, and metabolism therapeutic areas. The individual will lead cross-functional discussions, ensure regulatory compliance, and translate clinical data into accurate, consistent labelling content for global markets. They will also support health authority interactions and contribute to risk assessment and audit readiness.

Novartis

Hybrid Permanent

Senior Principal Statistical Programmer

Leads statistical programming for clinical studies across phases I-IV, ensuring high-quality, regulatory-compliant deliverables for regulatory submissions and clinical study reports. Develops and validates datasets and outputs using SAS, drives CDISC standards (SDTM/ADaM), and collaborates with biostatistics and cross-functional teams. Provides technical leadership, mentors junior programmers, and contributes to process improvements and programming specifications.

Novartis London, United Kingdom

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategy for GSK's global assets, with a focus on safety evaluation in immunology and other therapeutic areas. The Scientific Director will lead safety governance, contribute to regulatory submissions, and manage cross-functional teams to address product safety issues. They will also represent GSK in interactions with regulatory authorities and ensure compliance with global pharmacovigilance standards.

GSK £169,950 – £283,250 pa

On-site Permanent

SERM Scientific Director

Leads safety evaluation and risk management for GSK's oncology assets in clinical development, providing scientific expertise to assess and communicate safety risks globally. Works cross-functionally to shape safety strategy, support regulatory submissions, and ensure patient protection. Focuses on signal detection, risk assessment, and strategic decision-making in a matrix environment.

GSK £111,750 – £186,250 pa

On-site Permanent

SERM Scientific Director

Provides medical and scientific leadership in the safety evaluation and risk management of ViiV assets during clinical development. Interprets safety data, identifies and escalates safety signals, and delivers evidence-based recommendations to inform benefit-risk decisions. Engages with cross-functional teams, governance bodies, and regulatory authorities to shape the safety profile of specialty medicines and ensure patient safety.

GSK United Kingdom

Hybrid Permanent

Senior Director / Director, Oncology Translational Medicine Project Manager

This role leads the planning and execution of translational medicine strategies for GSK’s antibody-drug conjugate (ADC) oncology portfolio. The Director will integrate biomarker and diagnostic development with clinical programs, manage cross-functional teams, and ensure operational readiness for key milestones. They will provide strategic project management oversight, drive governance reporting, and support regulatory compliance across global oncology projects.

GSK Stevenage, United Kingdom

Hybrid Permanent

SERM Scientific Director

A senior scientific leadership role focused on pharmacovigilance and safety risk management for GSK's global pharmaceutical assets. The role involves leading safety strategy, evaluating clinical data, and ensuring regulatory compliance across development and post-marketing stages. It requires deep expertise in drug safety, cross-functional leadership, and communication with regulatory authorities.

GSK PLN 419,250 – PLN 698,750 pa

Senior Director / Director, Oncology Translational Medicine Project Manager

Leads end-to-end project management for GSK’s antibody-drug conjugate (ADC) translational medicine portfolio, integrating biomarker and diagnostic strategies across clinical development. Coordinates cross-functional teams and external partners to drive execution, governance readiness, and regulatory compliance. Focuses on strategic planning, risk management, and insight-driven reporting to support R&D decision-making.

GSK United States

Hybrid Permanent

SERM Medical Director

This role involves leading pharmacovigilance and risk management strategy for GSK’s global pharmaceutical assets, with a focus on patient safety across clinical development and post-marketing phases. The Medical Director will lead safety governance, drive signal detection and risk mitigation, and represent GSK in regulatory discussions. It requires deep expertise in drug safety, cross-functional leadership in a matrix environment, and strategic input into global safety operations.

GSK United Kingdom

On-site Permanent

SERM Medical Director

Provides medical and scientific leadership in the safety evaluation and risk management of GSK’s oncology assets in clinical development. Interprets safety data, identifies and escalates safety signals, and delivers evidence-based recommendations to support benefit-risk decisions. Engages with global governance, regulatory authorities, and cross-functional teams to shape the safety profile of innovative oncology medicines.

GSK €119,250 – €198,750 pa

On-site Permanent

Patient Activation Director - Respiratory / Hepatology

Leads global patient and physician engagement strategies to accelerate clinical trial enrolment in Respiratory and Hepatology indications. Develops patient-facing content, partners with advocacy groups, and leverages digital campaigns to improve trial awareness and recruitment. Works cross-functionally with Medical Affairs, Clinical Development, and external stakeholders to align activation efforts with scientific and regulatory standards.

GSK United Kingdom

Hybrid Permanent

Pipeline Acceleration Senior Director - Respiratory/Hepatology

Leads global medical affairs strategy for clinical trial acceleration within GSK’s Specialty Care pipeline, focusing on Respiratory and Hepatology. Drives field-ready scientific engagement through MSLs, investigator outreach, and patient activation to accelerate trial enrolment. Works cross-functionally to align medical strategy with R&D and Development Operations, ensuring coherent site engagement and robust scientific communication.

GSK United Kingdom

Hybrid Contract

Labelling Strategy and Development, Oncology Team Lead

Leads a global labelling team for oncology products, shaping clear and compliant regulatory labelling strategies across the product lifecycle. Interfaces with regulatory authorities and cross-functional teams to align labelling with patient care, commercial objectives, and compliance. Focuses on strategic governance, mentoring, and driving innovative approaches in oncology labelling.

GSK United States

Hybrid Permanent