493 jobs for “Clinical Research Physician”
Provides scientific and medical expertise at study level across early- and late-phase hepatology assets, leading protocol and study document development, serving as medical monitor for Phase 1-4 trials, and interpreting efficacy, safety and biomarker data. Works within cross-functional global study teams and mentors less experienced clinical scientists without formal line management.
Provides scientific and medical expertise at study level across early- and late-phase hepatology assets, leading protocol and study document development, serving as medical monitor for Phase 1–4 trials, and interpreting efficacy, safety and biomarker data. Works within cross-functional global study teams and the Clinical Matrix Team, with informal coaching of less experienced clinical scientists and no formal line management.
IQVIA
Site monitoring role covering selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines, plus recruitment tracking, protocol training and TMF/ISF documentation. Dedicated to a single sponsor within IQVIA's cFSP model, with access to large data pools to improve site selection and efficiency.
IQVIA
Monitors clinical trial sites across the UK, performing selection, initiation, monitoring and close-out visits in line with GCP and sponsor requirements. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains TMF/ISF documentation. Dedicated to a single sponsor within IQVIA's cFSP model.
Microsoft Word · Microsoft Excel · Microsoft PowerPoint
AstraZeneca · 10000+ people · Public
Accountable to the Global Clinical Head for an indication-aligned cluster of late-phase Respiratory and Immunology studies, supervising Global Development Medical Directors and Scientist Directors. Leads cross-functional design, conduct, monitoring and data interpretation, represents the program at health authority interactions, and co-leads publication strategy.
Fortrea
Leads clinical data management for one or more oncology studies within a sponsor-dedicated (FSP) model, acting as the primary client contact from study set-up through close-out. Combines strategic oversight of vendors, budgets and CDM deliverables with hands-on work such as eCRF design and data cleaning, collaborating with data coordinators and statistical programmers.
eCRF
Fortrea
Technical lead for all data management activities on late phase (IIb-III) clinical trials, from start-up through completion. Develops Data Management and Quality Management Plans, designs CRF/eCRF and database structures, and coordinates edit checks and discrepancy management. Acts as client liaison, tracking cycle times and metrics while overseeing data review staff.
RAVE · EDC
Thermo Fisher Scientific
Manages end-to-end clinical trial supply chains, developing study-specific plans, coordinating cross-functional teams, and ensuring GxP-compliant distribution and inventory levels. Represents the department externally, mentors junior staff, and drives process improvements within a global clinical supplies team.
Microsoft Office
Acorn by Synergie
Support the daily operational management of a Clinical Chemistry laboratory, performing routine and specialist testing, result validation, and analyser maintenance. Work with Beckman Coulter DxC700 AU, DxI 800 and DxA Automation Track systems, Remisol middleware and WinPath LIMS, participating in IQC/EQA and ISO 15189 compliance.
Beckman Coulter DxC700 AU · Beckman Coulter DxI 800 · Beckman Coulter DxA Automation Track +2
AstraZeneca · 10000+ people · Public
Lead digital health strategy engagements with AstraZeneca R&D, top pharma and biotechs, shaping operating models and roadmaps across clinical development. Directs project teams on AI and digital solutions such as ePRO/eCOA, wearables and digital biomarkers, building business cases and tracking value realisation. Combines consulting, protocol design support and scaled implementation in a matrixed environment.
ePRO · eCOA · Wearables +1
CSL · 10001+ people · Public
Leads a cross-functional Clinical Development Team as the lead scientific expert, owning the clinical strategy, plan and medical monitoring for immunoglobulin programs. Accountable for clinical content of regulatory submissions and study documents, and serves as medical monitor across trials in a matrixed environment.
CSL · 10001+ people · Public
Leads the cross-functional Clinical Development Team as lead scientific expert, owning the Clinical Development Plan and integrating internal and external contributions into program strategy. Serves as medical monitor, authors key regulatory and study documents, and presents to safety and review committees.
Isomorphic Labs · 201–500 people · Series A
Lead end-to-end clinical trial material planning, vendor management, packaging, labeling, inventory and global distribution for an AI-first drug discovery company. Act as the clinical supply authority within a lean Pharmaceutical Sciences & CMC team, building scalable systems and vendor networks while partnering closely with Clinical Operations and CROs.
IRT · RTSM
Bristol Myers Squibb
Leads clinical strategy and execution for one or more GI oncology indications of a given asset, owning the Target Product Profile and disease area strategy. Manages a team of physicians and scientists designing, running, analysing and interpreting all clinical studies, and acts as internal and external clinical authority for regulatory interactions and business development. Requires deep therapeutic expertise and 8+ years of drug development experience, with international and domestic travel.
Moderna · 1001–5000 people · Late stage
Lead development, qualification, validation and execution of complex cell-based immunoassays generating clinical trial data across therapeutic areas. Act as scientific point of contact within the Immuno-assays group, performing GCP/GLP-compliant sample testing, authoring validation reports, and mentoring junior lab staff. Fully onsite at Harwell, reporting to the Associate Director, Immuno-assay UK.
GraphPad Prism · Microsoft Word · Microsoft Excel +2
