Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory requirements and company policies.
Develop and maintain study protocols, case report forms, and other study-related documents.
Collaborate with cross-functional teams, including investigators, data managers, and medical writers.
Ensure timely and accurate reporting of study progress and results.
Manage and resolve issues related to study conduct, data quality, or patient safety.
Maintain accurate and up-to-date records of study activities and participants.

Job Requirements
Bachelor's degree in life sciences or a related field.
Proven experience in clinical research coordination, preferably in a pharmaceutical or CRO setting.




Solid knowledge of Positive Clinical Practice (GCP) guidelines and regulatory requirements.
Excellent communication, organizational, and problem-solving skills.
Ability to work independently and as part of a team.
Proficient in using clinical trial management systems (CTMS) and other relevant software tools.

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

📌 Clinical Research Coordinator Gurugram
🏢 Fortis
📍 Gurugram