Clinical Research Associate – Talent Pipeline Opportunity

About the role

Emerald Clinical Trials is expanding its European talent network and is looking for experienced Clinical Research Associates (CRA II or Senior CRA) to join a talent pipeline for upcoming projects. This position will support site activities across the clinical trial lifecycle and may progress as new studies are awarded.

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 trial master file records.
• Support investigators with training, relationship management, and study documentation.
• Assist recruitment and retention initiatives to meet study timelines.

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 abilities.
• Willingness and ability to travel regionally.
• Experience in renal, nephrology, cardiometabolic, or oncology studies is preferred.

Required skills

• ICH‑GCP compliance
• European regulatory knowledge
• Clinical trial site monitoring
• Data review and validation
• Documentation management

What we offer

• Purpose‑driven work contributing to therapies in renal, cardiometabolic, and oncology areas.
• Opportunity to join a global network of 800+ professionals.
• Potential for long‑term placement as new projects arise.