Latest Clinical Research Associate Jobs

Clinical Programmer/Analyst

The role involves developing, testing, and validating programming code to transform and analyze clinical and real-world data for use in regulatory submissions and scientific reporting. You'll collaborate with statisticians and data scientists to ensure outputs meet CDISC standards and regulatory requirements, while contributing to programming best practices within an agile environment. The position emphasizes code quality, compliance with GxP and ICH guidelines, and the use of modern tools and methodologies in a hybrid work setting.

GSK Stevenage, United Kingdom

Hybrid Permanent

Clinical Programmer/Analyst

The Clinical Programmer/Analyst designs, builds, and reviews programming solutions to transform clinical and real-world data into reliable, compliant outputs. Working closely with statisticians and data scientists, the role involves developing code for data transformation, analysis, and reporting in line with CDISC standards (SDTM, ADaM) and regulatory requirements. The position supports agile delivery of high-quality datasets, tables, listings, and figures while promoting programming best practices and innovation within a collaborative, cross-functional environment.

GSK United Kingdom

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading clinical development strategy for oncology, specifically lung cancer, providing medical oversight across trial design, safety monitoring, and data interpretation. The Senior Medical Director will guide cross-functional teams, engage with external experts, and contribute to regulatory submissions, ensuring patient-centred, scientifically rigorous development. Based in the UK with hybrid working, the position plays a key leadership role in advancing GSK’s oncology pipeline.

GSK Stevenage, United Kingdom PLN 593,250 – PLN 988,750 pa

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading clinical development in oncology, with a focus on lung cancer, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety monitoring, contribute to regulatory interactions, and mentor junior medical staff within a global matrix team. The position emphasizes strategic input, external scientific engagement, and integration of clinical insights to advance therapies for high unmet need.

GSK Switzerland

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading oncology clinical development for lung cancer programmes, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director ensures patient safety, guides cross-functional teams, and represents the programme in regulatory and scientific forums. Based on-site with a future relocation to Cambridge, UK, the position emphasizes strategic clinical leadership within a global biopharma environment.

GSK

On-site Permanent

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading oncology clinical development for lung cancer programmes, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director ensures patient safety, contributes to regulatory engagements, and mentors medical teams within a cross-functional environment. The position integrates physician expertise into clinical strategy and external scientific forums, focusing on advancing care in high unmet need cancers.

GSK

On-site Permanent

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading clinical development for oncology, specifically in lung cancer, by providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety monitoring, contribute to regulatory interactions, and mentor junior medical staff. The position requires deep expertise in oncology clinical trials and close collaboration with cross-functional teams and external experts.

GSK

Hybrid Permanent

Statistics Leader / Associate Director of Statistics

This role involves providing statistical leadership across oncology clinical development, from early-phase trials to regulatory submissions. The candidate will lead study design, analysis, and interpretation using advanced methods like Bayesian approaches and real-world data integration. They will collaborate with cross-functional teams to deliver robust statistical insights that inform key development decisions in a global biopharma environment.

GSK Stevenage, United Kingdom PLN 326,250 – PLN 543,750 pa

Statistics Leader / Associate Director of Statistics

Lead statistical strategy for oncology clinical development, from study design through regulatory submission, using advanced methods like Bayesian approaches and real-world data. Partner with cross-functional teams to deliver robust analyses and influence key decisions. Drive innovation in trial design and evidence generation within a global biopharma environment.

GSK United States £150,150 – £250,250 pa

Statistics Leader / Associate Director of Statistics

Lead statistical strategy across oncology clinical development, from early-phase trials to regulatory submissions, using innovative methods like Bayesian modeling and real-world data integration. Collaborate with cross-functional teams to design studies, analyze data, and communicate insights to non-technical stakeholders. Drive methodological innovation while ensuring statistical rigor in a matrixed, global environment.

GSK £150,150 – £250,250 pa

Statistics Leader / Associate Director of Statistics

Lead statistical strategy across oncology clinical development, from early-phase trials to registration, using innovative methods like Bayesian modelling and real-world data. Design studies, guide regulatory submissions, and influence asset strategy within a matrix environment. Work closely with cross-functional teams to deliver robust statistical insights for key decision-making.

GSK £326,250 – £543,750 pa

Statistics Leader / Associate Director of Statistics

This role involves providing statistical leadership across oncology clinical development, from early-phase trials to regulatory submissions. The candidate will design and analyze studies using advanced methods like Bayesian statistics, simulations, and real-world data, while collaborating with cross-functional teams. They will also drive innovation in statistical strategy and contribute to regulatory documentation and asset development.

GSK PLN 326,250 – PLN 543,750 pa

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation and benefit-risk management across clinical development and post-marketing settings. The position requires expert analysis of clinical and safety data, leadership in cross-functional governance teams, and strategic input into regulatory submissions and risk mitigation. It plays a critical part in ensuring patient safety and regulatory compliance within immunology and other therapeutic areas.

GSK United States US$169,950 – US$283,250 pa

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK’s global assets, with a focus on immunology. The Scientific Director will evaluate safety data, lead cross-functional teams, and ensure compliance in clinical development and post-marketing settings. The position requires deep expertise in safety evaluation, signal detection, and international regulatory standards.

GSK US$169,950 – US$283,250 pa

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation in immunology and other therapeutic areas. The Scientific Director will oversee safety governance, lead cross-functional teams, and ensure compliance with global regulations. They will analyze clinical data, manage safety issues, and contribute to regulatory submissions and long-term clinical strategy.

GSK US$169,950 – US$283,250 pa

On-site Permanent