Key responsibilities

• Coordinate all aspects of clinical trial activities from study start-up through to close-out.
• Manage participant recruitment, screening, follow-up visits, participant appointment bookings, laboratory sample processing and shipment.
• Ensure compliance with study protocols, GCP and ICH guidelines
• Prepare and maintain accurate trial documentation, source documents, and investigator site files.
• Collect, review, and enter study data into electronic data capture systems and CTMS.
• Track adverse events and ensure timely reporting in accordance with protocol and regulatory requirements.
• Coordinate investigational product accountability and study-related supplies.
• Support audit and inspection readiness activities.
• Maintain confidentiality and safeguard participant data at all times.

About you

Essential Requirements

• Minimum of 2 years' experience coordinating Sponsor initiated pharmaceutical clinical trials in a research, hospital, or healthcare setting
• Excellent participant care and participant facing soft skills
• Strong knowledge of ICH-GCP guidelines, clinical trial regulations, and ethics requirements
• Experience managing multiple studies simultaneously
• Excellent organisational, communication, and problem-solving skills
• High attention to detail and ability to meet deadlines
• Capability in prioritising workload and multitasking
• GCP R3 certification
• Ability to collaborate in a healthcare team and work independently
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