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Clinical Trials Coordinator at Rejuvenation Medical Group
Job Description & How to Apply Below
As a Clinical Trials Coordinator, you will need 2–3 years of related experience, alongside an MSc or BSc in clinical research. Your responsibilities will include supporting regulatory submissions, recruiting study participants, and maintaining accurate documentation using Real Time CTMS. This role is critical for the successful execution of clinical trials from start to finish, ensuring timely approvals and adherence to protocols.
Key Responsibilities:
• Oversee ethics and regulatory submissions for accuracy
• Coordinate clinical trial activities per protocols
• Recruit and enroll eligible study participants
• Schedule research visits and perform vital assessments
• Maintain comprehensive study documentation and records
Requirements:
• 2–3 years’ clinical research experience required
• MSc or BSc with clinical research experience preferred
• Knowledge of HREBA/IRISS submissions
• Experience in dermatology and aesthetics preferred
• Proficient in Microsoft Office applications
Bring your expertise in clinical research and communication to support Rejuvenation Medical Group's innovative trials.
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