Clinical Research Associate Jobs in England, United Kingdom

IQVIA UK’s Site Management team is expanding, focusing on oncology trials. The role monitors sites, ensures GCP compliance, manages recruitment, and maintains Trial Master Files.

Clinical Research team at AstraZeneca ensures high‑quality, compliant trials that bring life‑changing medicines to patients. The Clinical Research Associate drives study start‑up, site monitoring, data verification and regulatory compliance, collaborating with investigators and cross‑functional partners.

IQVIA UK’s Site Management (multi‑sponsor) team accelerates oncology trials by ensuring sites meet GCP and ICH standards. The role monitors sites, drives recruitment, trains staff, and resolves queries to keep studies on schedule.

Clinical Research Associate at IQVIA responsible for site monitoring, protocol training, quality oversight, and data management across oncology trials, ensuring GCP compliance and supporting recruitment.

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.

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.

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.

IQVIA Site Management team accelerates clinical research innovation across the UK. The Clinical Research Associate monitors oncology sites, conducts initiation, monitoring and close‑out visits, drives subject recruitment, ensures protocol compliance, and manages documentation and data queries. Manchester, United Kingdom, on-site with travel to sites, hybrid flexibility available.

IQVIA UK’s cFSP (sponsor‑dedicated) team accelerates innovation for a healthier world by delivering clinical research services. The Clinical Research Associate II conducts site monitoring visits, manages recruitment plans, ensures regulatory compliance, and collaborates with study teams across South East England.

IQVIA UK’s cFSP (sponsor-dedicated) team is expanding its Clinical Research Associate workforce in South East England to support innovative clinical studies. The role conducts site monitoring visits, drives subject recruitment, provides protocol training, ensures regulatory compliance, and manages study documentation and data queries.

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.

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.

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.

IQVIA UK’s Site Management team seeks a Clinical Research Associate II, Oncology to conduct site monitoring visits, manage study protocols, and ensure compliance with GCP and ICH guidelines. The role involves initiating, monitoring, and closing out visits, driving subject recruitment plans, administering protocol training, and maintaining Trial Master File and Investigator’s Site File records.

Join IQVIA on Our Mission to Drive Healthcare Forward. As a Clinical Research Associate at IQVIA, you’ll play a vital role in advancing clinical research and improving patient outcomes.

Novartis Clinical Research Associate Manager leads a field-based team in England/Wales, overseeing CRA performance and ensuring compliance with GCP and SOPs. The role drives hiring, training, and development of CRAs executing Phase I-IV global trials, while managing performance metrics and fostering a culture of ethical integrity.

SRS/FSP team at TFS HealthScience, a global CRO delivering clinical development solutions, ensures patient safety and data integrity across studies. The Clinical Research Associate conducts on-site and remote monitoring visits, reviews CRFs, manages investigational product accountability, and prepares monitoring reports.

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.

Clinical Research Associate to lead site performance and compliance in South East England. Responsibilities include site selection, monitoring, data integrity, regulatory documentation, and mentoring junior CRAs.

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.