Clinical Research Associate Jobs in Wales, 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.

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.

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.

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.

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.

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 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.

Fortrea Clinical Research Unit in Leeds builds early-phase clinical trials, monitoring Phase I–Ib studies on site. The CRA II role monitors dosing days, reviews source data, and collaborates with clinical, lab, and project teams to ensure protocol compliance.

IQVIA UK’s cFSP (sponsor‑dedicated) team is expanding its Clinical Research Associate roster in South West England to support interventional study monitoring and site management. The CRA conducts site monitoring visits, drives recruitment plans, trains sites, ensures regulatory compliance, and manages study documentation and data queries.

IQVIA UK’s cFSP (sponsor‑dedicated) team seeks experienced Clinical Research Associates to conduct site monitoring, drive recruitment plans, and manage study documentation across South West England. The role performs initiation, monitoring and close‑out visits, ensures GCP/ICH compliance, and collaborates 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.

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.

The Clinical Research Associate (CRA) ensures trial participant rights, data accuracy, and compliance with ICH GCP, local and global regulations, and Novotech SOPs. Acts as primary contact between sites, Novotech, and sponsors, managing site relationships, recruitment, monitoring visits, and data verification.

Clinical Research team at Pfizer ensures patient safety and high-quality execution of clinical trials. The Senior Clinical Research Associate II manages site activation, monitoring, and closeout, collaborates with investigators and internal partners, and resolves protocol and data issues.

Clinical Operations at Worldwide Clinical Trials is building a global CRO that innovates to improve patient lives. As a Senior Clinical Research Associate, you will qualify sites, conduct monitoring visits, mentor junior CRAs, and ensure protocol compliance across therapeutic areas such as CNS, Oncology, and Rare Diseases.

IQVIA UK Site Management team seeks experienced Clinical Research Associate to conduct site monitoring visits, drive recruitment, administer protocol training, evaluate site practices, track regulatory submissions, maintain TMF/ISF, generate reports, and collaborate with study teams.

IQVIA is seeking a Senior Clinical Research Associate to join its UK cFSP sponsor-dedicated team in Manchester. The role involves performing site monitoring visits—selection, initiation, monitoring, and close‑out—while ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

IQVIA Site Management team drives multi-sponsor clinical studies across oncology. The Senior Clinical Research Associate conducts site monitoring visits, manages recruitment plans, ensures regulatory compliance, and maintains study documentation.

Experienced Clinical Research Associate at IQVIA, part of the cFSP sponsor‑dedicated team in South West England. The role monitors clinical trial sites, ensuring GCP compliance, manages recruitment, data quality, and regulatory submissions.