Clinical Research Associate (CRA)

About the Role

We are seeking a motivated and detail-oriented Junior Clinical Research Associate (CRA) to join our team. This is an excellent opportunity for someone with at least one year of on-site monitoring experience, ideally gained within a CRO environment. The successful candidate will be responsible for monitoring clinical trials to ensure compliance with regulatory requirements, Good Clinical Practice (GCP), and study protocols.

Key Responsibilities

• Conduct on-site and remote monitoring visits to ensure compliance with study protocols, GCP, and regulatory requirements.
• Perform source data verification and ensure data accuracy and completeness.
• Build and maintain strong relationships with site staff to support study conduct and patient recruitment.
• Identify and resolve site-level issues, escalating as needed.
• Prepare and submit monitoring visit reports and follow-up documentation in a timely manner.
• Collaborate with internal teams to support study timelines and deliverables.

Requirements

• Minimum 1 year of independent monitoring experience in a clinical research setting.
• Experience working within a CRO or similar environment is acceptable.
• Strong understanding of ICH-GCP and clinical trial regulations.
• Excellent communication, organizational, and problem-solving skills.
• Ability to work independently and manage multiple priorities.
• Must be UK-based and able to work on-site in West London 2 days per week.
• Willingness to travel for site visits as required.
  
  

Preferred Qualifications

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Experience across multiple therapeutic areas is welcome but not essential.
  

Why Join Us?

• Competitive compensation and benefits package.
• Work with a collaborative, mission-driven team.
• Opportunities for professional development and internal growth.
• Contribute directly to the development of life-changing therapies.