Clinical Research Associate – Talent Pipeline Opportunity

About the role

Emerald Clinical Trials is expanding its European talent network and seeks experienced Clinical Research Associates (CRA II and Senior CRA) for future projects. This pipeline position will be considered as new studies are awarded, offering the chance to join a global leader in renal, cardiometabolic, and oncology research.

Key responsibilities

• Conduct site qualification, initiation, routine monitoring, and close‑out visits.
• Ensure protocol compliance, patient safety, and timely issue escalation.
• Review source documentation, validate study data, and maintain high‑quality records in study systems and TMF.
• Support investigators throughout the trial lifecycle and provide site training as needed.
• Manage site relationships and contribute to recruitment and retention initiatives.

Required profile

• Degree in Life Sciences or a related healthcare discipline.
• Minimum 2 years of independent monitoring experience in a CRO, academic, or pharmaceutical setting.
• Strong knowledge of ICH‑GCP and European regulatory requirements.
• Excellent communication and relationship‑building skills.
• Willingness to travel regionally.
• Experience in renal, nephrology, cardiometabolic, or oncology studies is preferred.

Required skills

What we offer

• Purpose‑driven work contributing to therapies that improve lives.
• Opportunity to join a global network of 800+ professionals.
• Exposure to diverse therapeutic areas and cutting‑edge clinical research.