Clinical Research Associate, UK

ICON; Reading; Remote; GBP 35,000 - 50,000; Full time

Job summary

A leading global biotechnology firm is seeking an experienced Regional Clinical Research Associate (CRA) based in the UK. This role offers a unique opportunity to work with a key client, providing monitoring and support for clinical study sites. The successful candidate will be responsible for ensuring compliance and driving site performance, while also contributing to investigator selection and training site staff. Join a team dedicated to addressing unmet medical needs and making a significant impact in the field of biopharmaceuticals.

Qualifications

• Over 2 years experience as a UK clinical research monitor or CRA.
• Residency in the UK with right-to-work.

Responsibilities

• Contribute to the selection of potential investigators.
• Provide monitoring visit reports within required timelines.
• Drive site performance and escalate issues.

Skills

Monitoring

Problem Solving

Job description

Job Title: Experienced UK-based Regional CRA

We are seeking an experienced UK-based Regional Clinical Research Associate (CRA) to join our existing CRA team at a multinational biopharmaceutical company.

About the Company: You will be part of an innovative, global biotechnology firm renowned as one of the world's leading independent biotechnology companies. The company focuses on areas with unmet medical needs, aiming to reduce the social and economic burden of disease.

Position Highlights: This role offers a rewarding opportunity with a key global client, supported by a strong internal team and mentoring/training plans. The hiring process involves a single internal interview with immediate feedback.

Main Responsibilities:

1. Contribute to the selection of potential investigators.
2. Provide monitoring visit reports within required timelines.
3. Drive site performance, proactively identify issues, and escalate as appropriate.
4. Perform source data verification according to SDV plan and resolve data queries.
5. Initiate, monitor, and close study sites in compliance with procedural documents. Share site progress and patient recruitment information within the Study Delivery Team.
6. Train, support, and advise investigators and site staff on study-related matters.

Qualifications and Requirements:

• Strong experience (approximately >2 years) as a UK clinical research monitor or CRA.
• Residency within the UK with appropriate right-to-work.
• Driving license is required.

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