- Conduct 3–4 daily field/site visits to doctors, hospitals, clinics, or research locations for coordination, relationship management, and study execution requirements.
- 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 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 qualified interaction with patients, healthcare professionals, and external research partners.

📌 Clinical Research Coordinator (Warangal)
🏢 Femacare Private
📍 Warangal