510 jobs for “Clinical Research Associate”
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
Thermo Fisher Scientific
Clinical Research Associate role within PPD's Functional Service Provider division, dedicated to a client and embedded in multi-national project teams. You perform and coordinate all aspects of clinical monitoring, conducting monitoring activities independently across challenging projects. Requires ICH-GCP, EU and FDA knowledge, with award-winning training provided.
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.
Pfizer · 10000+ people · Public
Accountable for planning and executing multiple complex global clinical studies, driving timelines, budgets and quality from study start-up through database release and inspection readiness. Leads cross-functional study teams, manages CRO vendor oversight, risk and quality metrics, and acts as the single authoritative source of study information for governance bodies.
Clinical Research Organization
Pfizer · 10000+ people · Public
Accountable for planning and executing multiple complex global clinical studies, driving timelines, budgets and quality targets while leading cross-functional study teams. Involves vendor and CRO oversight, risk management, governance presentations and inspection readiness, with program-level and submission support possible.
Clinical Research Organization
Leads the full statistical contribution to a clinical development programme, defining statistical strategy for trial design, analysis and regulatory submissions, and representing Biostatistics in interactions with the FDA, EMA and PMDA. Also manages outsourcing to CROs and internal statistical programmers, and supports departmental improvement initiatives.
SAS · R
Leads clinical development strategy for hepatology assets within GSK's Respiratory, Immunology & Inflammation Research Unit, from target identification through proof-of-concept studies. Accountable for clinical matrix team leadership, protocol design, medical monitoring and regulatory interactions across all development phases. Hybrid role with at least two on-site days weekly.
Thermo Fisher Scientific
Acts as independent Principal Investigator overseeing qualitative in-trial research studies, from design through delivery, for pharmaceutical clients. Applies methods like interviews and surveys to capture patient experience data, manages project budgets and timelines, and contributes to proposals and client development. Requires CAQDAS expertise and strong scientific writing.
Atlas.ti · NVivo · MAXQDA +1
Newcastle University · 5001–10000 people · Public
Investigates the molecular mechanisms of liver dysfunction in childhood POLG-related mitochondrial disease, focusing on Alpers-Huttenlocher syndrome. Uses quantitative untargeted proteomics and immunohistochemistry on donated post-mortem liver tissue, and generates hepatic organoids from patient-derived iPSCs for disease modelling and therapeutic screening. Based in the Newcastle Mitochondrial Research Group with a placement at the University of St Andrews.
iPSCs
Moderna · 1001–5000 people · Late stage
As an individual contributor in the Clinical Pharmacology group, you will develop quantitative strategies for dose selection, PK/PD characterization and regimen optimization across oncology, immunology and rare disease programs. You will partner with Pharmacometrics and QSP colleagues, represent CQP on program teams, and contribute to regulatory documentation and interactions.
R · Phoenix WinNonlin · NONMEM +2
Bristol Myers Squibb
Serves as primary medical accountability for Phase 1–3 clinical trials in neuroscience, leading medical monitoring, safety assessment and benefit/risk analysis within a matrixed study delivery team. Partners with clinical scientists on protocol design, site interactions and health authority submissions, and builds relationships with principal investigators and thought leaders.
Helical
Hands-on business development role researching pharma and biotech accounts, writing outreach, and owning CRM pipeline hygiene in HubSpot. Works directly with founders and the head of sales, building sales materials and AI workflows while coordinating with the science team ahead of customer meetings.
HubSpot · LinkedIn
AstraZeneca · 10000+ people · Public
Leads an integrated Business Continuity and Crisis Management capability across Oncology R&D, owning the framework, risk registers and BIAs while designing executive-level crisis exercises. Drives emerging-risk assessment, supply-chain nth-tier visibility and the practical use of AI in resilience practice, acting as the audit and regulatory interface for standards such as NIS2.
NIS2 · Business Continuity Software
AstraZeneca · 10000+ people · Public
Leads the strategy, design, execution and reporting of post-authorisation safety studies using real-world data such as EHR, claims and registries. Provides epidemiological input to regulatory deliverables including Risk Management Plans, signal evaluations and FDA diversity plans, while mentoring CROs and academic partners across multiple therapy areas.
EHR · Claims Data · Registries +1
