Clinical Research Associate Jobs in Wales, United Kingdom

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 cFSP team seeks an Experienced Clinical Research Associate to accelerate innovation for a healthier world. The role involves performing site monitoring visits, managing study progress, and ensuring regulatory compliance in Reading or Manchester.

Precision Medicine Group is a specialized CRO focused on precision oncology. As a Clinical Research Associate II you will monitor and own the progress of clinical studies, coordinate site setup activities, and ensure compliance with protocol, SOPs, ICH‑GCP and regulatory standards.

Clinical Operations team at BeOne Medicines UK drives oncology clinical trials from start-up to closeout. The Clinical Research Associate monitors sites, ensures regulatory compliance, manages data collection, and collaborates with the Regional Clinical Operations Manager to meet study timelines.

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.

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 UK’s cFSP (sponsor‑dedicated) team accelerates innovation for a healthier world by managing clinical research studies. The Senior Clinical Research Associate conducts site monitoring visits, drives subject recruitment, ensures regulatory compliance, and maintains trial documentation.

Clinical Research team at NAMSA conducts global medical device trials ensuring patient safety and regulatory compliance. The Associate monitors sites, conducts qualifications, initiations, interim and close‑out visits, and manages study documentation and metrics.

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 Operations at Worldwide Clinical Trials is building a global team of Clinical Research Associates to advance oncology and neurology studies. The Senior CRA will qualify sites, conduct monitoring visits, mentor junior staff, and ensure protocol compliance while managing documentation and data queries.

Clinical Operations Department at Worldwide Clinical Trials drives high‑quality clinical research across oncology, CNS and rare disease studies. The Senior Clinical Research Associate leads site qualification, initiation, monitoring, and close‑out visits, mentors junior CRAs, and ensures protocol adherence and data integrity.

Clinical Research Physician at Pulse Healthcare, part of the Acute Doctors team, conducts and oversees clinical trials to advance medical knowledge while ensuring regulatory compliance. The role involves managing trial protocols, patient safety, data analysis, and stakeholder communication.

Clinical Research Team at Pulse Healthcare drives innovative clinical trials to improve global health outcomes. The nurse conducts participant visits, assessments, and safety checks, records data in eCRFs, and supports patient recruitment and retention.

Pulse Healthcare Clinical Research Nurse team advances global health outcomes by conducting innovative clinical trials. The role conducts participant visits, assessments, data entry, and emergency response within study protocols.

Clinical Research Team at Pulse Healthcare drives innovative clinical trials to improve global health outcomes. The nurse conducts participant visits, assessments, and safety checks, records data in eCRFs, and supports patient recruitment and retention.

Clinical Research Team at Pulse Healthcare drives innovative clinical trials to improve global health outcomes. The nurse conducts participant visits, assessments, and safety checks, records data in eCRFs, and supports recruitment and retention across multiple therapeutic areas.

Clinical Research Team at Pulse Healthcare focuses on advancing global health outcomes through innovative clinical trials. The Clinical Research Nurse conducts participant visits, assessments, and safety checks, records data in eCRFs, and supports recruitment and retention.

Clinical Research Team at Pulse Healthcare drives innovative trials to improve global health outcomes. The nurse conducts participant visits, assessments, safety checks, and data entry for multiple therapeutic studies while supporting emergency response and MDT meetings.

Thermo Fisher Scientific (PPD Clinical Research Services) seeks an Executive Account Director, Business Development – Biopharma to secure and retain business with the top 25 global biopharma companies. Day-to-day, you will orchestrate RFP strategy, develop proposals, negotiate and close contracts, conduct cold calls and client visits, ensure client satisfaction, and mentor junior staff, focusing on clinical research studies phases II and III. This remote role spans multiple European countries in