Clinical Research Coordinator

Job Description – Clinical Research Coordinator Company: Cosma Fertility Position: Clinical Research Coordinator Location: Andhra Pradesh, Telangana, Karnataka,Lucknow Job Type: Remote, On-field work at their location Employment Type: Full-Time Working Days: 6 Days a Week Work Timings: 10:00 AM to 7:00 PM About the Role Cosma Fertility is seeking a dedicated and detail-oriented Clinical Research Coordinator to support and manage clinical research activities in the field of fertility and reproductive healthcare. The candidate will play a key role in coordinating clinical trials, maintaining documentation, interacting with doctors and patients, and ensuring compliance with clinical research protocols and regulatory standards. Key Responsibilities  Coordinate and manage the day-to-day operations of clinical trials in accordance with study protocols.  Recruit, screen, and enroll eligible participants while ensuring proper documentation.  Generate and manage lead collection for clinical trials through various channels including doctor referrals, campaigns, databases, and outreach programs.  Obtain informed consent from participants and ensure clear understanding of study procedures, risks, and benefits.  Ensure strict adherence to clinical trial protocols, SOPs, GCP guidelines, and regulatory requirements.  Maintain accurate, complete, and up-to-date study records, reports, and clinical documentation.  Collaborate with investigators, doctors, and cross-functional research teams for smooth execution of clinical studies.  Conduct regular site visits and coordinate with doctors regarding study progress and operational requirements.  Monitor participant progress, manage follow-ups, and address study-related concerns in a timely manner.  Assist in data collection, data entry, query resolution, and maintenance of data integrity.  Support audit and inspection readiness by ensuring proper compliance and documentation management.  Prepare presentations, reports, and updates related to study progress and clinical outcomes for stakeholders.  Identify operational challenges and coordinate solutions to ensure timely completion of clinical trials.  Maintain professional interaction with patients, healthcare professionals, and external research partners. Required Skills & Qualifications  Good knowledge of Clinical Research and clinical trial processes  Understanding of GCP (Good Clinical Practice) and regulatory guidelines  Strong communication, coordination, and interpersonal skills  Excellent documentation and organizational abilities  Ability to interact professionally with doctors, patients, and research teams  Strong attention to detail and problem-solving skills  Ability to manage multiple tasks in a fast-paced environment Preferred Qualifications  M. Pharma / Life Sciences background preferred  Certification in Clinical Research preferred  Internship or prior experience in Clinical Research is an added advantage