CRA / Sr. CRA (Clinical Trial)
Required Experience – 2 Years to 8 Years
Required Qualification – Any Science Graduate
Location - Ahmedabad, Delhi, Mumbai, Lucknow, Jaipur, Nasik, Nagpur, Pune, Kolkata, Bangalore, Hyderabad, Chennai
- Perform Site Identification and conduct Feasibility Studies. Perform Site Selection Visit, Site Initiation Visits in accordance with the protocol and other applicable regulatory
- guidelines including local regulatory guidelines. Perform Site Monitoring Visit and Site Close-Out Visit in accordance with the protocol and other applicable
- regulatory guidelines including local regulatory guidelines. Send Follow Up letters to sites and submit Visit Reports to the Clinical Team Leader/ Project Manager as
- required. Keep a close association with site (s) for: Patient Recruitment, Patient Follow Up, and protocol related activities. Act as a communication Link between Sponsor and the site. Maintain accurate and timely sponsor/site correspondence and communication. Attend Investigators Meeting. Training of Investigators on Protocol and other applicable regulatory guidelines including local regulatory
- guidelines. Ethics Committee Submission
- Help in preparation of Regulatory Binder. Maintain updated Site Files and collection of the essential documents and project related documents during the
- site visits and maintain Central Clinical File. CRF retrieval as per the project instructions. Coordinate and distribute Clinical Study Material to study sites. Archival of study documents.