Latest Clinical Research Associate Jobs

Medical Director-Oncology Clinical Development - GI

Serves as the physician within a clinical programme team, leading medical monitoring and safety oversight for oncology studies and interpreting clinical and safety data. Partners with the Senior Scientist and cross-functional teams on protocol development, regulatory interactions and investigator engagement, with a focus on GI oncology. Requires an on-site office presence two to three days a week.

GSK London US$222,750 – US$371,250 pa

Hybrid

Medical Director-Oncology Clinical Development - GI

Serves as the physician on a clinical programme team, leading medical monitoring and safety oversight for GI oncology studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators and regulators. Works within a Clinical Matrix Team alongside Clinical Operations, Biostatistics, Regulatory and Pharmacovigilance, with on-site presence 2-3 days a week.

GSK Waltham, United States US$222,750 – US$371,250 pa

Hybrid

Senior Medical Director, Oncology Clinical Development - Sarcoma

Senior physician leader providing medical oversight, safety evaluation and clinical data interpretation across sarcoma oncology studies, from protocol design through regulatory interaction. Serves as a senior member of the Clinical Matrix Team, mentoring Medical Directors and engaging external experts, with a minimum two-day on-site office presence.

GSK Zug, Switzerland US$284,250 – US$473,750 pa

On-site

AI Director, Development Global Clinical Operations

Drives an AI-native strategy for clinical operations, framing hypotheses and building working agentic AI prototypes hands-on before scaling them into production with enterprise technology teams. Combines strategy, solution architecture and build-buy-partner decisions, including vendor evaluation, business cases and GxP-validated deployment, working with R&D leaders and frontline users.

GSK Upper Providence US$179,850 – US$299,750 pa

Executive Medical Director, Clinical Development Lead - Oncology GU

Owns the clinical strategy, scientific narrative and benefit-risk framework for a genitourinary oncology asset, acting as the senior clinical authority on the Medicine Development Team core quad. Sets asset-level evidence-generation and governance strategy while study-level delivery is led by Senior Scientists, and represents Clinical Development in health authority interactions, advisory boards and alliance partnerships. Also mentors clinical development talent and applies AI-enabled analytics to sharpen development decisions.

GSK USA - Pennsylvania - Upper Providence US$284,250 – US$473,750 pa

Hybrid

Senior Medical Director, Oncology Clinical Development - Sarcoma

Senior physician leader providing medical oversight, safety monitoring and clinical data interpretation across sarcoma oncology studies, from protocol design through regulatory interactions. Serves as a senior member of the Clinical Matrix Team, mentoring Medical Directors and engaging external experts, advisory boards and health authorities.

GSK USA - Pennsylvania - Upper Providence US$284,250 – US$473,750 pa

On-site

Principal Programmer Analyst

Lead programming activities for one or more clinical studies, developing, maintaining and validating complex analysis packages to CDISC and Good Programming Practice standards. Act as technical mentor to junior programmers and lead programming support for regulatory interactions with the EMA and FDA. Works in an agile, squad-based team bridging scientific requirements with technical solutions, with R proficiency preferred.

GSK London

Hybrid

Principal Programmer Analyst

Leads statistical programming for complex and pivotal clinical studies, developing, maintaining and validating analysis packages while ensuring compliance with Good Programming Practices and CDISC standards. Acts as a technical mentor to junior programmers and leads programming support for regulatory interactions with bodies such as the EMA and FDA, working in an agile, squad-based team alongside clinical, statistical and operational stakeholders.

GSK Stevenage

Hybrid

Principal Programmer Analyst

Lead programming activities for complex and pivotal clinical studies, developing, maintaining and validating analysis packages while ensuring compliance with Good Programming Practices and CDISC standards. Mentor junior programmers, support regulatory interactions with EMA and FDA, and bridge scientific requirements with technical solutions in an agile, squad-based global team.

GSK USA - Pennsylvania - Upper Providence

Hybrid

SERM Principal Scientist

Provides medical and scientific expertise in safety evaluation and risk management for GSK products across clinical development and post-marketing settings. Responsible for signal detection, benefit-risk assessment, authoring risk management plans and aggregate safety reports, and supporting inspection readiness. Works within a cross-functional matrix team, escalating safety issues to governance bodies and supporting risk-reduction strategies in protocols and labelling.

GSK London

Hybrid

Senior, Forward Deployed Engineer (Digital Twin & Optimization)

Embedded with chemical manufacturing teams, you take AI use cases from problem framing to working prototypes at days-to-weeks cadence, building in-silico process models, digital twins and optimization solutions. Work is AI-augmented, with coding agents handling routine development while you supply judgement, validation and model identification. Proven solutions are packaged for handoff to a solutions engineer for scale-up.

GSK London

Hybrid

Senior, Forward Deployed Engineer (Digital Twin & Optimization)

Embedded with chemical manufacturing teams, you build in-silico process models, digital twins and optimization solutions, taking proofs of concept to deployed MVPs at a days-to-weeks cadence. Work is AI-augmented, with coding agents handling routine development while you focus on model identification, scenario planning and handing proven solutions to solutions engineers.

GSK Stevenage

Hybrid

SERM Senior Scientific Director, Oncology

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents the Safety Evaluation & Risk Management function on cross-functional clinical matrix and project teams, escalating emerging safety issues to senior governance. Mentors junior staff and partners with Safety Physicians to shape long-term safety strategy.

GSK London

SERM Senior Scientific Director, Oncology

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents SERM on cross-functional clinical matrix teams, escalates emerging safety issues to governance bodies and mentors junior staff within a global matrix environment.

GSK Poznań, Poland PLN 525,750 – PLN 876,250 pa

SERM Senior Scientific Director, Oncology

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents SERM on cross-functional clinical matrix teams, escalates emerging safety issues to governance bodies and mentors junior staff within a global matrix.

GSK Wavre, Belgium €141,000 – €235,000 pa