Clinical Research Associate – Talent Pipeline Opportunity

About the role

Emerald Clinical Trials is building a European talent network and seeks experienced Clinical Research Associates (CRA II and Senior CRA) for future project assignments. This pipeline role will be considered as new studies are awarded, offering the chance to join a global leader in clinical 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.
• Assist with recruitment and retention initiatives and manage site relationships.

Required profile

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

Required skills

• ICH‑GCP
• European regulatory requirements

What we offer

• Opportunity to work with a global leader in clinical research.
• Purpose‑driven projects improving patient outcomes.
• Access to a diverse, international professional network.