Latest Clinical Research Associate Jobs

Experienced Clinical Research Associate

Monitors clinical trial sites across selection, initiation, monitoring and close-out visits, ensuring compliance with GCP and ICH guidelines. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within a sponsor-dedicated team, liaising with sites and study team members.

IQVIA Reading

Senior Clinical Research Associate - FSP - South West England

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. Conducts onsite and remote monitoring visits, source data review and verification, and case report form review, while managing site quality risk assessments and maintaining CTMS and eTMF documentation. Works within a local study team supporting a key sponsor, with a focus on ICH GCP compliance, patient safety, and inspection readiness.

Parexel London

Remote

Senior Clinical Research Associate I/II - Sponsor Dedicated - Oncology Experience Needed

Lead monitoring activities for assigned oncology clinical trial sites, from site activation through closeout, conducting both onsite and remote visits, source data verification and regulatory document oversight. Partner with a dedicated sponsor in an FSP model, driving enrollment, resolving protocol deviations and supporting audit readiness. Requires at least five years of oncology clinical research experience and up to 75% travel.

Parexel London

Remote

Intern Clinical Operations

A 12-month clinical operations internship supporting trial setup, execution and closure across the UK, liaising with hospital sites and research staff and assisting with regulatory submissions and data monitoring. The intern collaborates with Clinical Research Associates and Start-Up Specialists and gains exposure to feasibility, patient recruitment and site management, working remotely with proximity to the Leeds headquarters.

Fortrea Maidenhead

Remote Internship

CRA II, Oncology

Monitors oncology clinical trial sites through selection, initiation, monitoring and close-out visits, ensuring compliance with GCP and ICH guidelines. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within IQVIA UK's multi-sponsor Site Management team, with travel to sites required.

IQVIA Manchester

CRA I/II/ Sr CRA - FSP - UK

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.

Thermo Fisher Scientific United Kingdom

Remote

Senior Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

Develops, validates and runs ligand-binding and cell-based bioanalytical assays generating pharmacodynamic and immunogenicity data for clinical mRNA programmes. Works in a GcLP-regulated lab using Thermo Watson LIMS and electronic notebooks, handling clinical samples, critical reagents, SOPs and validation reports while partnering with Clinical Operations and Sample Management.

Moderna Oxford

Hybrid Permanent

Clinical Research Nurse II

Conducts multiple ongoing clinical trials, handling informed consent, screening, vital signs, ECGs and protocol procedures while ensuring subject safety and accurate data capture. Engages across site operations including recruitment, enrolment and retention, working with research site and interdepartmental teams under FDA/GCP and ICH regulations.

Thermo Fisher Scientific Manchester

Contract

Sr. Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

Develop, validate and run ligand-binding and cell-based bioanalytical assays generating pharmacodynamic and immunogenicity data for clinical mRNA programmes. Testing clinical samples in a GcLP-regulated lab using Thermo Watson LIMS, with documentation, SOPs and validation reports, partnering with Clinical Operations and Sample Management.

Moderna Clinical Development

Hybrid Permanent

Associate Director, Biostatistics

Leads the full statistical contribution to a clinical development programme, defining statistical strategy and methodology for trial design, analysis and regulatory submissions. Represents Biostatistics in interactions with FDA, EMA and PMDA, manages CRO/FSP outsourcing, and provides thought partnership on innovative study design and Go-No Go criteria. Two positions available across multiple therapeutic areas.

CSL Amsterdam, Netherlands US$212,000 – US$251,000 pa

Hybrid Permanent

Associate Director, Biostatistics

Leads the full statistical contribution to a clinical development programme, defining statistical strategy and methodology for trial design, analysis and regulatory submissions. Represents Biostatistics in interactions with FDA, EMA and PMDA, manages CRO/FSP outsourcing, and provides thought partnership on Go-No Go criteria and probability of technical success. Hybrid role requiring at least three days onsite weekly.

CSL Maidenhead US$212,000 – US$251,000 pa

Hybrid

Clinical Development Medical Director- Hepatology

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.

GSK London US$202,500 – US$371,250 pa

Hybrid

Clinical Development Medical Director- Hepatology

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.

GSK Boston, United States US$222,750 – US$371,250 pa

Hybrid

Sr Clinical Development Scientist

Supports late-stage oncology clinical development in collaboration with a Clinical Scientist Program Lead, covering study start-up, execution, close-out, data analysis and regulatory filings. Involves drafting protocols and CRFs, reviewing data and contributing to submissions, with a focus on CAR T-cell and multiple myeloma programmes.

Gilead Sciences London

Associate Director, Global Clinical Physician - Neuroscience

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.

Bristol Myers Squibb Uxbridge