We are looking for a highly motivated and detail-oriented individual to join our team as an Assistant Research Coordinator- Clinical in Sangath. The ideal candidate will have a strong background in clinical research and excellent organizational skills.

Roles and Responsibility

- Coordinate and manage clinical trial data, ensuring accuracy and compliance with regulatory requirements.

- Develop and maintain study protocols, informed consent forms, and other clinical documents.

- Collaborate with cross-functional teams, including investigators, statisticians, and medical writers.

- Conduct site monitoring visits to ensure adherence to study protocols and safety regulations.

- Prepare and review study reports, such as progress and final study reports.

- Ensure timely resolution of issues related to study conduct or patient safety.

Job Requirements

- Bachelor's degree in Life Sciences or a related field.





- Minimum 2 years of experience in clinical research, preferably in a coordinating role.

- Strong knowledge of Good Clinical Practice (GCP) principles and regulations.

- Excellent communication, organizational, and problem-solving skills.

- Ability to work independently and collaboratively within a team workplace.

- Proficiency in using clinical trial management systems (CTMS) and other relevant software tools.

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📌 Assistant Research Coordinator- Clinical (New Delhi)
🏢 Sangath
📍 New Delhi