Clinical Trial Coordinator

About the Role

Cure Talent is pleased to partner with a well-established and expanding healthcare organization dedicated to advancing clinical studies across Europe and globally. We are seeking a Clinical Trial Coordinator to join their team and contribute significantly to study execution and site interaction. This role is central to coordinating multi-center, multi-country clinical studies. You will collaborate closely with the Clinical Project Manager and various internal teams to ensure studies adhere to schedules, maintain strong site engagement, and uphold high standards for data and documentation.

Key Responsibilities

• Monitor the progression of studies, including site activation, participant recruitment, and data input, ensuring adherence to project timelines.
• Serve as a primary liaison for investigational sites, facilitating daily communication and engagement.
• Assist with site initiation processes, such as gathering necessary documentation and verifying readiness.
• Track key study performance indicators, identify potential risks or setbacks, and report them as needed.
• Oversee vendor deliverables and facilitate coordination among external partners, study sites, and internal departments.
• Maintain and audit the Trial Master File (TMF), ensuring its completeness and readiness for inspections.
• Supervise data entry into Electronic Data Capture (EDC) systems and the resolution of data queries, ensuring consistency with study progress.
• Provide consistent progress reports to the Clinical Project Manager and other relevant stakeholders.

The Ideal Candidate

• Demonstrated experience in clinical research, either with a sponsor organization or a Contract Research Organization (CRO).
• Proven track record of supporting multi-center, international clinical studies.
• Proficiency with Good Clinical Practice (GCP) guidelines and the European clinical research landscape.
• Experience utilizing EDC systems and managing Trial Master Files (TMF) or electronic TMFs (eTMF).
• Exceptional organizational abilities, capable of managing multiple tasks simultaneously and independently driving follow-up actions.
• Excellent communication skills, effective for engaging with study sites and diverse project teams.

This is an excellent opportunity to join a collaborative clinical team and contribute to the successful delivery of international studies in a dynamic environment.