497 jobs for “Clinical Data Manager/ Snr Clinical Data”
Individual contributor role supporting forward deployed engineering pods at GSK's manufacturing sites, driving opportunity discovery, value sizing, scoping and hands-on prototyping. You work directly with production, planning, quality and training teams, iterating on data, model outputs and workflows until AI solutions are adopted on the floor.
Excel · SQL · Python +2
Leads CMC's scientific data, application and agentic AI product portfolio, setting integrated strategy and roadmap across forward-deployed engineering, product management and AI product strategy. Accountable for delivery quality, GxP compliance, governance, budget and headcount, and for representing the capability to R&D, Global Supply Chain, Quality and enterprise leadership.
IQVIA
Monitors clinical trial sites across the UK, handling selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines. Manages multiple protocols, drives subject recruitment, tracks regulatory submissions and CRF data, and maintains Trial Master File documentation. Based in Reading with regular travel to investigative sites.
IQVIA
Conducts site qualification, initiation, monitoring and close-out visits for clinical trials, ensuring GCP compliance, patient safety and data integrity. Builds relationships with investigators, resolves data queries, mentors junior staff and travels up to 40-60% within the region. Embedded in a sponsor-dedicated functional service partnership model.
Investigator Site Files · Trial Master Files
Parexel
Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review while managing risk-based quality and regulatory compliance. Works within a local study team supporting a key sponsor, with travel across the UK and internationally.
CTMS · eTMF
Parexel
Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review. Works within a local study team for a key sponsor, using CTMS, eTMF and risk-based quality management, with travel across the UK and internationally.
CTMS · eTMF
Recursion · 501–1000 people · Series C
Lead clinical pharmacology and pharmacometrics strategy across a portfolio of rare disease and oncology programs, serving as the clinical pharmacology lead for regulatory interactions and study design from Phase 1-3. Perform and oversee modeling and simulation with tools such as WinNonlin, Monolix, NONMEM and R, and author regulatory sections for IBs, INDs and NDAs. Part of a Pharmacometrics team spanning clinical pharmacology, pharmacometrics and translational modeling, working end-to-end across discovery and development.
WinNonlin · Monolix · NONMEM +1
Recursion · 501–1000 people · Series C
Lead clinical pharmacology and pharmacometrics strategy across a portfolio of rare disease and oncology programs, serving as the clinical pharmacology lead and regulatory representative. Oversee modeling and simulation (population PK, PK-PD, exposure-response) and provide pharmacology input on Phase 1-3 study designs. Work cross-functionally with clinical, translational and discovery teams in an end-to-end drug development environment.
WinNonlin · Monolix · NONMEM +1
Fortrea
Lead and manage clinical trial sites across a diverse portfolio spanning oncology, neuroscience, cell & gene and CAR-T therapies. The role emphasises patient safety, data integrity and building trusted relationships with investigators, with autonomy and support for complex, innovative study designs.
Fortrea
Monitors clinical trial sites across a diverse portfolio spanning oncology, neuroscience, general medicine, cell & gene and CAR-T therapy. Leads site management, builds relationships with investigators and study teams, and safeguards patient safety and data integrity on complex, first-in-class studies. Distinct for its breadth across therapeutic areas and advanced therapy exposure rather than a narrow single-indication focus.
Acts as the primary interface between business stakeholders, biostatisticians, statistical programmers and technical delivery teams, translating clinical and statistical requirements into scalable R-based analytics, automation workflows and enterprise reporting. Leads requirement workshops, manages a small team, and oversees releases with end-to-end traceability, regulatory compliance and audit readiness across the clinical trial lifecycle.
Co-leads cross-functional Clinical Trial Teams and global studies from planning through close-out, managing timelines, budgets, risks and inspection readiness. Partners across global and local functions on recruitment, data operations and vendor performance, while championing operational excellence and continuous improvement.
Moderna · 1001–5000 people · Late stage
Designs and delivers immunogenicity and bioanalytical strategies for regulated clinical programmes, developing ADA, nAb, PK and PD assays using ELISA, MSD and cell culture. Works with multidisciplinary teams to validate assays, manage reagents and SOPs, and integrate digital and AI-enabled tools. Site-based at Harwell within a growing mRNA-focused team.
ELISA · MSD · LIMS +2
AstraZeneca · 10000+ people · Public
Lead multidisciplinary teams defining and delivering AstraZeneca's frontier AI roadmap, turning ambiguous scientific and business questions into scalable AI/ML and agentic systems deployed on cloud and HPC. The role spans problem framing, MLOps, governance and external partnerships, with a strong emphasis on reuse, adoption and measurable scientific impact.
Python · PyTorch · JAX +7
AstraZeneca · 10000+ people · Public
Leads three mandates for an infectious disease portfolio: defining end-to-end publication strategy from target selection to clinical development, securing grants and partnerships with NGOs and philanthropic funders, and horizon-scanning emerging biotechnology. Partners with discovery, clinical, data and external academic stakeholders, coaching teams and influencing senior decision-makers.
