Clinical Research Coordinator (M.Pharm)
About the Role
Roles & Responsibilities
• Coordinate and manage clinical research studies as per protocol and regulatory guidelines
• Assist in patient recruitment, screening, and follow-up visits
• Maintain study documentation, case report forms (CRFs), and regulatory files
• Ensure compliance with GCP, ICH, and institutional guidelines
• Coordinate with investigators, sponsors, and ethics committees
• Monitor data accuracy, reporting timelines, and study progress
• Support audit and inspection readiness activities
Qualification
• M.Sc / M.Pharm (Master of Pharmacy) from a recognized institute
Experience
• Relevant clinical research experience preferred
Age Limit
• Minimum: 21 years
• Maximum: 45 years
Number of Vacancy: 07 Posts
Skills
• Knowledge of clinical research processes and GCP guidelines
• Strong documentation and data management skills
• Effective communication and coordination abilities
• Attention to detail and regulatory compliance awareness
About the Organization
Advanced Centre for Treatment Research and Education in Cancer (ACTREC), a premier cancer research and treatment institution, focuses on advancing oncology research, clinical trials, and patient care through high-quality scientific and clinical excellence.
Walk-in Interview Details
Date: 06-03-2026
Venue: Mahamana Pandit Madan Mohan Malviya Cancer Centre, Sunder Bagiya, B.H.U Campus, Varanasi, Uttar Pradesh – 221005
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