Study Coordinator

Overview

Position summary:

• Recruit and screen participants, obtain informed consent, and ensure protocol compliance.
• Collect and document data accurately, maintaining records per GCP standards.
• Liaise with investigators, sponsors, and study monitors.

Experience Requirements

Key responsibilities will include:

• Recruiting and screening participants,
• Obtaining informed consent,
• Ensuring compliance with study protocols and regulatory requirements.
• Managing patient visits,
• Collecting and documenting data accurately,
• Maintaining proper records in line with Good Clinical Practice (GCP) standards.
• Liaising with investigators, sponsors, and study monitors,
• Managing study supplies,
• Ensuring the timely and efficient execution of the trial.
• Playing a crucial role in maintaining the safety and well-being of participants while ensuring the integrity of the clinical data collected.