Education
- Associate degree in Life Sciences
Experience
Requisites for the Role
- Strong analytical skills
- Basic understanding of clinical trials
- Good documentation management
- Excellent communication
- Resilient and adaptable
Roles and Responsibilities
- Perform as a member of the project team with the goal to contribute towards efficient management of trials.
- Communicates effectively with site personnel and DRK supervisor to update the study tracker with latest study status.
- To update the study tracker with latest safety updates from allocated sites.
- Liaises with site to resolve data discrepancies and ensures all study goals are met as per supervisor’s instruction.
- Initiates payment requests for investigators (If required).
- Performs other duties as assigned by management.
- Logistics support to CRM and CRAs.
- Maintain the study files as per supervisor’s instructions.
- Assist with the preparation, distribution, and tracking of study documents such as protocols, informed consent forms, investigator brochures, and study manuals. Maintain Trial Master File (TMF) and ensure completeness and audit readiness according to SOPs and ICH-GCP guidelines.
- Support site start-up activities, including collection and review of essential documents and coordinating ethics submissions.
- Schedule and coordinate meetings, prepare agendas, take minutes, and track action items.
- Update and maintain clinical trial management systems (CTMS), electronic Trial Master File (eTMF), and other study databases.
- Assist in the tracking of study metrics, enrollment, and timelines.
- Liaise with clinical research associates (CRAs), sites, and vendors to ensure timely communication and resolution of issues.
- Support clinical supply management, including tracking and distribution of investigational product (IP) and study materials.
- Assist in preparation for audits and regulatory inspections
- Perform other duties as assigned by management.
Deadline To Apply
November 30 , 2025
Job Type: Full-time
Pay: From Rs45,000.00 per month
Work Location: In person