Job Description
We are looking for a Clinical Research Coordinator to support the planning, execution, and administration of clinical studies in accordance with approved protocols and regulatory requirements. The candidate will coordinate with investigators, participants, and sponsors, maintain study documentation, and ensure accurate data collection throughout the research process.
Responsibilities
• Coordinate clinical trial activities in line with study protocols
• Recruit and schedule study participants and follow-up visits
• Maintain regulatory files, informed consent forms, and study documentation
• Collect, verify, and update clinical research data and case records
• Communicate with investigators, sponsors, and ethics committees regarding study requirements
• Recruit and schedule study participants and follow-up visits
• Maintain regulatory files, informed consent forms, and study documentation
• Collect, verify, and update clinical research data and case records
• Communicate with investigators, sponsors, and ethics committees regarding study requirements
Skills & Qualifications
Experience Required
1–4 years
Required Skills
Clinical Documentation
Clinical Trial Coordination
Data Collection & Reporting
Good Clinical Practice (GCP)
Regulatory Compliance
Languages
English
Education
Bachelor's Degree (Undergraduate)