Clinical Research Coordinator

Role & Responsibilities
• Recruit and enroll eligible study participants
• Coordinate patient visits, procedures, and follow-ups as per study protocol
• Enter and maintain clinical research data in electronic data capture (EDC) systems
• Address protocol-related queries from study participants
• Ensure compliance with ICH-GCP, ethical guidelines, and regulatory requirements
• Prepare, maintain, and update essential study documentation
• Archive Case Report Forms (CRFs) and trial-related documents properly
• Coordinate with sponsors, ethics committees, investigators, and study sites
• Support Principal Investigators (PI) for smooth study conduct

Qualifications & Experience
• Bachelor’s or Master’s degree in Biotechnology, Biochemistry, Microbiology, Biology, Life   Sciences, Nursing, or Pharmacy
• Diploma in Clinical Research (optional)
• 1–5 years of experience in clinical research coordination
• Strong understanding of clinical trial processes and documentation
• Proficiency in MS Word and MS Excel
• Good communication and interpersonal skills

About the Company
• Indira IVF Hospital is one of India’s leading fertility and reproductive healthcare organizations,    known for its hospital-based clinical research and patient-centric trials.