Clinical Trial Coordinator

Contract length:
Short term contract with possibility of extension

About the Role

An exciting opportunity has become available for a Clinical Research Coordinator to support the delivery of innovative clinical studies.

This position is ideal for someone with previous clinical research experience who enjoys working in a fast-paced environment and wants to play a key role in the successful execution of clinical trials.

Responsibilities

• Coordinate day-to-day clinical trial activities from study start-up through to close-out.
• Support participant recruitment, screening and enrolment activities.
• Schedule study visits and maintain accurate study documentation.
• Ensure all study files are maintained in accordance with GCP and regulatory requirements.
• Collect, review and enter study data while ensuring quality and accuracy.
• Support monitoring visits, audits and inspections.
• Assist with regulatory submissions and essential document management.
• Act as a key contact between participants, investigators, sponsors and study vendors.
• Track study progress and assist with milestone delivery.

Requirements

• Previous experience as a Clinical Research Coordinator, Clinical Trial Coordinator, Study Coordinator, Research Nurse or similar clinical research role.
• Good understanding of ICH-GCP guidelines and clinical trial processes.
• Experience working with study documentation and data collection activities.
• Excellent organisational and communication skills.
• Ability to manage multiple priorities and work to deadlines.
• Degree in Life Sciences, Nursing, Pharmacy, Biomedical Science or a related discipline is advantageous.