Clinical Research Coordinator

Roles & Responsibilities
• Assist in compilation and maintenance of study-related documents during the pre-trial and ongoing study phases
• Support Ethics Committee (EC) submissions, follow-ups, and approval processes
• Ensure site setup and conduct activities in accordance with approved study protocols
• Coordinate and schedule subject visits, including scheduled and unscheduled visits
• Fix subject appointments in consultation with the site investigator
• Explain study procedures, protocols, and requirements to trial subjects
• Address and resolve non-medical queries from study participants
• Provide regular updates to investigators on study activities and progress

Qualification
• B.Pharm (Bachelor of Pharmacy)
• B.Sc in Biology, Microbiology, or Life Sciences

Experience
• 1–2 years of experience in clinical research or clinical operations
• Hands-on exposure to site coordination, study documentation, and subject management preferred

Skills
• Knowledge of clinical trial coordination and site operations
• Understanding of GCP guidelines and protocol adherence
• Experience with Ethics Committee submissions and regulatory documentation
• Strong coordination, communication, and organizational skills
• Ability to interact effectively with investigators, subjects, and study teams

About the Company
PFC Pharma Focus India is a clinical research organization supporting end-to-end clinical trial operations across multiple therapeutic areas. With a strong presence in Delhi NCR, the company focuses on quality-driven research, regulatory compliance, and efficient site management, offering professionals valuable exposure and growth opportunities in clinical research and clinical operations.