Clinical Trials Coordinator

Summary:

The Clinical Trials Coordinator plays a vital role in the health and safety sector by overseeing the planning, execution, and management of clinical trials. This position is essential for ensuring compliance with regulatory standards and facilitating effective communication among stakeholders. The coordinator will contribute to advancing medical research and improving patient outcomes through meticulous coordination and support of clinical studies.

Responsibilities:

• Coordinate and manage all aspects of clinical trials, including site selection, patient recruitment, and data collection
• Ensure compliance with regulatory requirements and ethical standards throughout the trial process
• Maintain accurate and up-to-date trial documentation, including protocols, consent forms, and case report forms
• Facilitate communication between investigators, sponsors, and regulatory bodies to ensure smooth trial operations
• Monitor trial progress and report on key performance indicators to stakeholders
• Assist in the training and supervision of trial staff and ensure adherence to study protocols
• Prepare and submit necessary reports and documentation to regulatory authorities as required

Qualifications:

• Bachelor’s degree in a relevant field such as life sciences, nursing, or health-related discipline is preferrable
• Clinical trial coordination experience or a related role
• Strong understanding of Good Clinical Practice (GCP) and regulatory requirements
• Excellent organisational and time management skills, with the ability to manage multiple tasks simultaneously
• Strong communication and interpersonal skills to effectively liaise with diverse stakeholders
• Proficient in using clinical trial management software and Microsoft Office Suite
• Attention to detail and a commitment to maintaining high standards of quality and accuracy