
Duties of a Clinical Trials Study Coordinator
10 hours ago
As a Clinical Trials Study Coordinator, you will play a pivotal role in the management of clinical trials at our medical centre.
The ideal candidate will possess relevant tertiary qualifications and experience working as a Clinical Trials Co-ordinator. A solid understanding of clinical trials, including trial phases, is also essential.
- Coordinate all aspects of allocated clinical trials, ensuring seamless execution from initiation to close-out.
- Prepare for and host site visits, participant visits, and maintain accurate records.
- Maintain open communication with sponsors, CRAs, and monitors, addressing any queries or concerns promptly.
Key responsibilities include:
Attending remote and on-site Site Initiation Visits for delegated trials
Preparing and conducting participant visits
Completing associated documentation, maintaining study binders, and other relevant documentation
Additional duties may include:
Maintaining investigational product and performing accountability
Working closely with the recruitment team to ensure timely and efficient recruitment
Professional development opportunities are available to support your growth and success in this dynamic role.
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