Clinical Research Associate Jobs in England, 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.

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 (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.

We are currently recruiting for Clinical Research Associate II and Senior Clinical Research Associate to join our Multi-Sponsor Clinical Trials Team in the UK. This role if fully decentralised in the UK. Your time here At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they’re set up for success.

Senior Clinical Research Associate (CRA) role at Thermo Fisher Scientific's PPD division in the UK. Responsible for coordinating all aspects of clinical monitoring and site management, conducting remote or on-site visits to assess protocol and regulatory compliance, and managing required documentation. Acts as a site processes specialist ensuring trials adhere to approved protocol, ICH‑GCP guidelines, regulations and SOPs to protect subject rights, well‑being and data reliability.

Join Us on Our Mission to Drive Healthcare Forward. IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.

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.

Parexel FSP’s Oncology Clinical Research team drives patient‑centric trials across Europe. The Senior CRA manages site activation, monitoring, AE/SAE reporting, audit coordination and CAPA implementation for oncology studies.

Worldwide Clinical Trials is a global midsize CRO advancing treatments for persistent diseases, with a focus on CNS and Oncology. As a Senior Clinical Research Associate, you will manage research activities at sites for predominantly non-interventional and observational studies, handling site identification, start-up, training, maintenance, and close-out.

Clinical Research Team at Fortrea drives innovative clinical trials across the UK. The CRA II/SCRA II conducts site monitoring, initiates and closes studies, ensures GCP compliance, and mentors junior staff while traveling to sites in the Midlands. Remote work model with occasional travel to Maidenhead and surrounding sites.

Parexel’s Oncology Clinical Research team drives patient‑centric trials across the UK. The Senior CRA ensures data integrity, GCP compliance, and remote monitoring of oncology sites, collaborating with Site Managers and investigators to keep studies on track. London, Remote – full‑time, hybrid model with 3 days onsite optional.

Field-based CRA position Reporting to Clinical Operations Manager Excellent development opportunities, reward and benefits package Job Overview Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging advanced capabilities to drive industry leading performance. Partners with study teams, AbbVie internal R&D stakeholders, investigators, and site staff for meaningful and effective engagements positioning AbbVie as the

You’ll be responsible for the operational leadership and delivery of assigned ophthalmic medical device clinical studies throughout the study lifecycle, from concept and study design through start-up, execution, close-out and reporting. Working in close partnership with Clinical Scientists and cross-functional stakeholders, the Senior Clinical Research Associate acts as the operational study lead for assigned studies, providing expertise in study planning, site selection, budget development, ven

As a Clinical Research Associate I you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators.

Start your clinical research career helping to shape the future of diabetes care. We currently have an exciting opportunity for an aspiring Clinical Research Associate (CRA) to join our Clinical Affairs team in Witney.

As a Clinical Research Associate, you will be the primary face of our studies at assigned sites, ensuring excellence from start-up through close-out. You will collaborate closely with local study leadership and cross-functional partners to uphold the highest standards of quality, compliance and patient safety.

As a Clinical Research Associate, you will be the primary face of our studies at assigned sites, ensuring excellence from start-up through close-out. You will collaborate closely with local study leadership and cross-functional partners to uphold the highest standards of quality, compliance and patient safety.

As a Clinical Research Associate, you will be the primary face of our studies at assigned sites, ensuring excellence from start-up through close-out. You will collaborate closely with local study leadership and cross-functional partners to uphold the highest standards of quality, compliance and patient safety.

As a Clinical Research Associate, you will be the primary face of our studies at assigned sites, ensuring excellence from start-up through close-out. You will collaborate closely with local study leadership and cross-functional partners to uphold the highest standards of quality, compliance and patient safety.

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates.