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 is intended to build a pool of qualified professionals who can be deployed as new study awards arise.

Key responsibilities

• Conduct site qualification, initiation, routine monitoring, and close‑out visits.
• Ensure protocol compliance and patient safety.
• Review source documentation and validate study data.
• Support investigator sites throughout the clinical trial lifecycle.
• Manage site relationships and provide training as required.
• Identify and escalate issues in a timely manner.
• Maintain high‑quality documentation within study systems and TMF.
• Support recruitment and retention initiatives.

Required profile

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

Required skills

• ICH‑GCP knowledge
• Understanding of European clinical trial regulations

What we offer

• Opportunity to work on global Phase I‑IV clinical trials.
• Collaboration with leading biotech and pharmaceutical companies.
• Purpose‑driven environment focused on renal, cardiometabolic and oncology therapies.