Clinical Research Associate – Talent Pipeline

About the role

Emerald Clinical is building a talent pipeline for Clinical Research Associates (CRA II and Senior CRA) to support upcoming European studies. This position is a pipelining role, with hiring progressing as new projects 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 documentation in study systems and TMF.
• Support investigators throughout the trial lifecycle and provide site training as needed.
• Assist with recruitment and retention initiatives.

Required profile

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

Required skills

• ICH‑GCP
• European regulatory compliance
• Clinical trial monitoring

What we offer

• Opportunity to join a global leader in clinical research.
• Potential for future project assignments across Europe.
• Exposure to a diverse portfolio of therapeutic areas.