499 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.
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.
Leads clinical development strategy for hepatology assets within the Respiratory, Immunology & Inflammation Research Unit, overseeing study design, medical monitoring, and regulatory interactions. Accountable for the Clinical Matrix Team, target validation, translational plans, and Go/No Go decision criteria across early-phase programs. Hybrid role requiring on-site presence at least two days per week.
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
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
Johnson & Johnson Innovative Medicine
Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, conducts proactive safety data reviews, and serves as product point of contact, with hybrid working requiring three days on site.
Microsoft Word · Microsoft Excel · Microsoft PowerPoint
Relation Therapeutics
Lead the team behind hybrid on-prem and cloud compute infrastructure, Kubernetes clusters, and scientific compute environments supporting ML and drug discovery. Own platform strategy, CI/CD maturity, observability, and security controls for sensitive patient-derived data, reporting to the VP of Engineering.
Kubernetes · Kubeflow · GPU Compute +3
University of Exeter
Computational PhD project using cell-free DNA sequencing to infer placental gene activity and dissect how genetic variants linked to adverse pregnancy outcomes affect placental function. The student develops tools to map nucleosomal footprints, integrates them with single-cell RNA-seq markers and GWAS summary statistics, and may generate new plasma data.
scRNA-seq · cfDNA Sequencing · GWAS
Moderna · 1001–5000 people · Late stage
Leads the creation, review and oversight of investigator site budgets and grants across Phase I–IV clinical trials, using Grants Manager/GrantPlan and FMV benchmarking. Manages CRO site budget and CTA negotiations, scenario planning and site activation timelines, with exposure to Generative AI tools for analytics.
Grants Manager · GrantPlan · MS Office +1
