. This role offers an excellent opportunity to contribute to high-quality research and collaborate with global stakeholders in clinical development.
Key Responsibilities:
Coordinate daily study activities at site.
Support investigators with patient recruitment, scheduling, and follow-up.
Ensure compliance with protocol, ICH-GCP, and regulatory requirements.
Manage study documentation and facilitate monitoring visits.
Qualifications & Experience:
Bachelor's degree in Medicine, Pharmacy, Dentistry or life sciences.
Previous experience as a Study Coordinator,
with proven expertise in dermatology studies.
Strong understanding of clinical trial operations and GCP.
Excellent organizational, communication, and interpersonal skills.
Location:
UAE
Engagement:
Full-time, site-based
If you meet the criteria and are looking to advance your career in clinical research, we welcome your application.
Job Type: Full-time
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