Clinical Research Associate – Talent Pipeline Role

About the role

Emerald Clinical Trials is building a European talent pool for Clinical Research Associates. This pipeline position targets experienced CRA II and Senior CRA professionals who will be considered for upcoming study assignments across Europe.

Key responsibilities

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

Required profile

• Degree in Life Sciences or a related healthcare discipline.
• Minimum two 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 to travel regionally.

Required skills

• ICH‑GCP
• European regulatory requirements

What we offer

• Opportunity to join a global leader in clinical research with a purpose‑driven focus on renal, cardiometabolic and oncology therapies.
• Access to a network of professionals and future project assignments as studies are awarded.