Clinical Research Coordinator

Roles & Responsibilities
• Coordinate day-to-day clinical trial activities at the study site
• Assist investigators in patient screening, recruitment, and follow-up visits
• Maintain and update Trial Master File (TMF) and essential study documents
• Ensure compliance with ICH-GCP guidelines and approved study protocols
• Support and document the informed consent process
• Perform data entry and resolve queries in CRF/eCRF systems
• Communicate with sponsors, CROs, and ethics committees
• Prepare study reports and maintain regulatory documentation
• Support monitoring visits and audits

Qualification
• B.Sc / M.Sc or equivalent degree in Life Sciences
• Master of Pharmacy

Experience
• Minimum 1 year of clinical research experience
• Experience in site coordination and clinical trial documentation preferred

Skills
• Understanding of clinical trial processes
• Basic knowledge of ICH-GCP guidelines
• Strong documentation skills
• Proficiency in CRF/eCRF systems
• Good communication and coordination abilities
• Attention to detail and compliance awareness

About the Organization
A leading clinical research services provider based in Delhi, India, offering structured clinical trial management solutions. The organization provides strong exposure to clinical operations, regulatory documentation, and sponsor coordination within a professional research environment.