Clinical Research Coordinator

Role & Responsibilities
• Coordinate day-to-day clinical trial activities at the site
• Manage subject recruitment, screening and follow-up visits
• Maintain source documents, essential trial files and study logs
• Perform accurate data entry in EDC systems
• Ensure compliance with study protocols, GCP and regulatory guidelines
• Support investigators and clinical research teams during trial conduct
• Assist during monitoring visits, audits and inspections
• Ensure timely documentation and reporting

Qualification
• Degree or Diploma in Pharmacy, Life Sciences, Nursing or Allied Health Sciences

Experience
• Minimum 1 year of experience as a Clinical Research Coordinator

Skills
• Basic understanding of clinical research processes
• Knowledge of GCP and ICH guidelines
• Strong communication and coordination abilities
• High attention to detail and data quality orientation
• Effective documentation and time-management skills

About the Company
Canvass Clinical Research Services Pvt. Ltd. is a growing clinical research organization providing comprehensive site management and clinical trial coordination services, offering professionals hands-on exposure, structured learning and strong career growth opportunities in the clinical research domain.