Clinical Research Associate Jobs in United Kingdom

The Clinical Research Associate will oversee clinical trials, ensuring adherence to protocols and regulations. Responsibilities include site management, monitoring, and collaboration with internal and external stakeholders to drive successful trial execution and patient care advancements.

Clinical Research Associate 2 role at IQVIA involves monitoring clinical trial sites to ensure compliance with GCP and ICH guidelines. The associate conducts site visits, manages recruitment plans, administers protocol training, and maintains trial master files.

Study Delivery team at AstraZeneca ensures high‑quality clinical trials from start‑up to close‑out. The Clinical Research Associate will lead site start‑up, regulatory maintenance, risk‑based monitoring and data verification, conducting both remote and onsite visits while collaborating with investigators and cross‑functional partners.

Site Management and Monitoring teams across Oncology and Cell Therapy at AstraZeneca build and oversee high‑quality clinical trials. The Clinical Research Associate owns site activation and performance, conducts risk‑based monitoring, and ensures patient safety and data integrity through onsite and remote visits.

Clinical Research Associate on Merck’s global clinical research team, driving site performance and compliance across the South East. Day‑to‑day duties include site selection, monitoring, data integrity checks, and cross‑functional coordination with regulatory, pharmacovigilance, and finance teams.

Clinical Research Associate on Merck’s Clinical Research team, driving ICH/GCP compliance and site performance across North West England. Day‑to‑day duties include site selection, monitoring, data integrity checks, and mentoring junior CRAs while coordinating cross‑functional stakeholders.

Clinical Research Associate role at Canaan Valley Institute supports ophthalmic medical device trials. Responsible for coordinating study documentation, ensuring GCP compliance, managing site interactions, and overseeing investigational product traceability.

Clinical Research Associate – IQVIA Biotech is a full‑time role based in Reading, Berkshire, United Kingdom. The position supports the acceleration of clinical development for biotech partners by conducting site monitoring visits, managing study progress, and ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Merck’s Clinical Research Associate team in London drives high‑quality trials across the UK. The role leads site performance, monitoring, and compliance for protocols in the South East, coordinating cross‑functional tasks and mentoring junior CRAs. London, Remote, 65–75% travel, with a focus on patient safety and regulatory excellence.

AstraZeneca is expanding its Biopharma and Oncology teams, hiring Clinical Research Associates to start in March/April 2026. The role focuses on site activation, risk‑based monitoring, and ensuring compliance with ICH‑GCP and local regulations.

Our Sponsor Dedicated (cFSP) team is growing and we are looking for aspiring CRAs of all levels to join us on our mission to drive healthcare forward. We offer cutting‑edge medicines, access to significant data pools for better site selection, genuine career development opportunities, stable workload, and tools such as an iPad, site visit app and site visit report app to make the CRA role more efficient.

Clinical Research Associate (CRA) at AstraZeneca delivers studies at sites, ensuring compliance with ICH‑GCP, GMP, GDP, local regulations, and study procedures. Acts as main contact with sites, trains staff, monitors and closes sites, manages supplies, conducts data checks, performs risk assessments, resolves queries, reports adverse events, prepares reports, escalates concerns, supports audits, and maintains inspection‑ready documentation.

ProPharma seeks a Serbian-speaking Clinical Research Associate for an 18‑month fixed‑term contract. Responsible for monitoring clinical sites in person and remotely, conducting study start‑ups, developing monitoring documentation, reviewing source documents and case reports, managing investigational supplies, monitoring enrollment and adverse events, reviewing regulatory documents, communicating with site personnel and cross‑functional teams, and participating in project meetings.

IQVIA's Site Management team seeks a Clinical Research Associate to support oncology studies across UK sites. Responsibilities include site monitoring visits, recruitment planning, protocol training, quality assessment, regulatory submission tracking, TMF/ISF maintenance, documentation, and collaboration with study teams.

Clinical Research Associate at Novotech, a global CRO, ensures trial participants’ rights and data integrity while managing site relationships. The role involves monitoring sites, coordinating regulatory submissions, and driving participant recruitment across the UK. On-site work in the United Kingdom with flexible hours and supportive benefits.

Clinical Operations (multi-sponsor) team at FTMAI Fortrea Development Ltd in the UK is building a fast‑paced, innovative global CRO. The CRA I role monitors national oncology trials, including solid tumors and hematology, using a risk‑based model to drive smarter trial management. The position requires at least 6 months of independent monitoring experience and a passion for diverse therapeutic areas such as ophthalmology and neuroscience.

Ora’s Clinical Research Associate II (CRA II) builds strong site relationships to ensure compliant, high‑quality ophthalmic trials. The role monitors sites, reviews data, and coordinates with cross‑functional teams to maintain protocol integrity.

Cell Therapy Site Management & Monitoring (SMM) at AstraZeneca partners with investigators to initiate, run and close advanced cell therapy studies, ensuring compliance and patient access. The CRA drives start‑up, monitoring visits, data verification and regulatory maintenance, collaborating with Local Study Managers and site staff.

Biopharma and Oncology teams at AstraZeneca design and deliver patient‑centric clinical trials across therapeutic areas. The Clinical Research Associate will own site activation and performance, conduct risk‑based monitoring, and ensure data integrity and patient safety through onsite and remote visits.

Cell Therapy Site Management & Monitoring (SMM) at AstraZeneca partners with investigators to initiate, run and close advanced cell therapy trials, ensuring compliance and rapid patient access. As a Clinical Research Associate you’ll manage start‑up, monitoring visits, data verification and regulatory documentation for Australian sites, collaborating with Local Study Managers and using Veeva Clinical Vault.