Clinical Research Coordinator

Job Clinical Research Coordinator

Description – Clinical Research Coordinator

Company: Cosma Fertility

Position: Clinical Research Coordinator

Employment Type: Full-Time

Preferred Candidate: Male Candidate

Working Days: 6 Days a Week

Work Timings: 10:00 AM to 7:00 PM

Locations:

· Hyderabad

· North India Region

· Kolkata

· Nepal

. Lucknow

. Gorakhpur

.Kanpur

.Varansi

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 3–4 daily field/site visits to doctors, hospitals, clinics, or research locations for coordination, relationship management, and study execution requirements.

· Conduct regular site visits and doctor interactions to align on study progress, patient recruitment, and clinical trial 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

· Willingness to travel and conduct daily field/site visits as required

· 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

Why Join Us

· Opportunity to work in an innovative fertility and reproductive healthcare startup

· Exposure to advanced clinical and research-driven projects

· Collaborative and growth-oriented work environment

· Opportunity to work closely with medical experts and clinical research professionals