490 jobs for “Clinical Trials Pharmacist”
Serves as the physician within a clinical program team, leading medical monitoring and safety oversight for genitourinary oncology studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. Hybrid role with at least two days per week on-site.
AI
Serves as the physician within oncology clinical program teams, leading medical monitoring, safety oversight and clinical data interpretation for genitourinary cancer studies. Partners with the Senior Scientist and cross-functional Clinical Matrix Team on protocol development, investigator engagement and regulatory interactions, with hybrid working of at least two days on-site per week.
AI
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.
R
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.
R
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.
R
Owns operational delivery of diagnostics across early and late-stage oncology trials, covering biosample collection, processing and storage, and implementation of clinical trial assays at reference and central labs and CROs. Works in a matrix with biomarker, clinical operations, data management, regulatory and procurement colleagues, managing vendors, contracts and data transfer agreements while keeping studies audit-ready.
Owns operational delivery of diagnostics across early and late-stage oncology trials, from biosample collection and clinical trial assays at reference and central labs to audit-ready data. Works in a matrix with Diagnostic Strategy, Biomarker, Clinical Operations, Data Management, Regulatory, Quality and Procurement, plus external CROs, labs and vendors, and mentors colleagues as a subject matter expert.
CRO
Owns operational delivery of diagnostics across early and late-stage oncology trials, from biosample collection and clinical trial assays at reference and central labs to analysis-ready, audit-ready data. Works in a matrix with strategy, biomarker, clinical operations, data management, regulatory, quality and procurement teams, plus external CROs, labs and vendors, and mentors colleagues as a subject matter expert.
CRO · Central Labs · Reference Labs
Leads cross-functional project teams within Oncology Translational Medicine, coordinating diagnostics, biomarker, clinical development, regulatory and finance activities across internal groups and external partners. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations of diagnostic technologies.
Microsoft Project · Microsoft Word · Microsoft Excel +7
Leads cross-functional project teams within Oncology Translational Medicine to progress diagnostic and biomarker development activities, coordinating with clinical, regulatory, quality, finance and external lab partners. Builds integrated timelines, tracks budgets, milestones and contracts, mitigates risks, and supports regulatory submissions and technical evaluations of diagnostic technologies.
Microsoft Project · Microsoft Word · Microsoft Excel +7
Leads cross-functional project teams within Oncology Translational Medicine, coordinating diagnostics, biomarker and clinical development activities with internal groups and external labs and manufacturers. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations of diagnostic technologies.
Microsoft Project · Microsoft Word · Microsoft Excel +7
Leads cross-functional project teams within Oncology Translational Medicine to advance diagnostic and biomarker development programs, coordinating internal groups and external labs and Dx manufacturers. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations. Hybrid role requiring 2-3 days per week onsite.
Microsoft Project · Microsoft Word · Microsoft Excel +7
Individual-contributor alliance lead owning the relationship with an established central laboratory partner, balancing strategic direction with day-to-day governance and delivery oversight. Embeds a new operating model, monitors KPIs and study delivery, resolves escalations, and uses AI tools such as Claude to analyse large datasets and drive continuous improvement.
Claude
Individual-contributor alliance lead owning an established central laboratory partnership, balancing strategic direction with hands-on governance. Runs governance forums, monitors KPIs and study delivery, resolves urgent operational issues, and embeds a new operating model, using AI tools to analyse large datasets.
Claude
Senior physician leader providing medical oversight, safety monitoring and clinical data interpretation across lung cancer studies within a clinical programme team. Partners with the Senior Scientist and cross-functional groups on protocol design, regulatory interactions and external scientific engagement, while mentoring Medical Directors. Requires an on-site presence at least two days a week.
