Clinical Research Coordinator

Role & Responsibilities
• Oversee, manage, and coordinate clinical trials as per approved protocols and regulatory requirements
• Obtain informed consent and ensure adherence to ethical clinical research practices
• Manage study protocols and maintain strict documentation standards
• Ensure regulatory compliance throughout the study lifecycle
• Maintain accurate and up-to-date study records and research documentation
• Coordinate with investigators, medical staff, and multidisciplinary research teams
• Support smooth execution and timely completion of clinical research activities

Qualifications & Experience
• B.Pharm, M.Pharm, PharmD, B.Sc / M.Sc Life Sciences or related field
• Demonstrated clinical research or clinical trial experience
• Strong knowledge of ICH-GCP and regulatory requirements

Skills
• Excellent documentation and record-keeping abilities
• Strong organizational, time management, and problem-solving skills
• Effective communication and stakeholder coordination skills
• Ability to work collaboratively within multidisciplinary teams

Preferred
• Advanced degree or certification in clinical research

About the Company
• Research-focused clinical organization based in Prayagraj conducting regulated clinical trials