Clinical Research Coordinator

Roles & Responsibilities
• Recruit and enroll eligible study participants as per approved protocols
• Coordinate patient visits, procedures, follow-ups, and study schedules
• Enter, review, and maintain accurate clinical data in EDC systems
• Act as primary point of contact for study participants and address protocol-related queries
• Ensure compliance with ICH-GCP, ethical guidelines, and regulatory requirements
• Prepare, maintain, and update essential study documents and trial files
• Manage proper filing and archival of CRFs and study-related documentation
• Coordinate with sponsors, ethics committees, investigators, and multiple study sites
• Support Principal Investigators (PI) for smooth conduct of clinical studies

Qualification
• Bachelor’s or Master’s degree in Biotechnology, Biochemistry, Microbiology, Life Sciences, Nursing, Pharmacy, or related discipline
• Diploma in Clinical Research is an added advantage

Experience
• 1-5 years of experience in clinical research coordination or site operations
• Hospital-based or site-level research experience preferred

Skills
• Strong knowledge of clinical trial processes and documentation
• Working understanding of ICH-GCP and regulatory requirements
• Good data management, organizational, and planning skills
• Proficiency in MS Word and MS Excel
• Strong communication and interpersonal skills
• Ability to coordinate with multiple stakeholders and sites

About the Company
Indira IVF Hospital is one of India’s leading fertility and reproductive healthcare organizations, known for its extensive national presence, patient-centric approach, and commitment to clinical excellence, research, and ethical medical practices in assisted reproductive technologies.