The St. John's Research Institute (SJRI) is a part of the St John's National Academy of Health Sciences, which is run by the CBCI Society for Medical Education. From its inception, St. John's has set before it an ideal of excellence in academic courses as well as service to society as a result of which it has truly become holistic both in its outlook and in its approach to the problems of community health. In 2000, the Academy decided that its commitment to excellence in research required the setting up of an Institute that was dedicated to the pursuit of research and capacity development in St. John's. This vision encompassed improvement of health of the community and patients through research and development of a Center for Excellence in medical research in India.
Post : Project Technical Support II - Analytical Project
Job Summary : The study is a multicentre randomized control trial which involves the assessment of malabsorption in stunted children. The study will involve interaction with children and their parents, IEC, Lab staff and other departments in the institution. The conduct of the study should be according to ICH GCP Guidelines. Should assist the Principal Investigator and Co investigators in screening of subjects by maintaining and updating the list of potentially eligible patients for the ongoing study and supervise the protocol.
Key Responsibilities :
Coordinate screening, enrolment, periodic study visits and close out visit.
1. Ensure that rights and well-being of a research participant is protected throughout the duration of the study.
2. Assure all study documentation is maintained by completing the source documents for each
3. Completing CRFs, e-CRFs on time and resolve data queries.
4. EDC, Inform & Medidata data capture.
5. Ensure and maintain inventory of Study consumables like Investigational product handling, storage, dispensing, accountability, tracking temperature, calibration of equipment’s, sample centrifugation, courier of documents and lab samples shipment.
6. Timely preparation, notification and tracking of the Ethics committee submissions.
7. Submission of the study progress, amendments, Protocol Deviations, AE's and SAEs to the ethics committee and sponsor in a timely manner.
8. Coordinate with the investigator and the safety monitoring team at the time of SAEs.
9. Assist in resolving IEC and DSMB queries.
10. Follow up with patients and document in telephone contact report.
11. Conduct study closeout visit and archive the documents
Eligibility Criteria
Preferred Qualifications : Clinical research e.g. Diploma in clinical research , or BSC or MSC Clinical research, nutrition or Pharm D
Minimum Experience : No. required : fresher
Maximum Experience : No. required : 1 year
Preferred Language : English, Kannada & Telugu
Location : Bangalore
Tentative Date of Joining : 15th May 2026
To Apply : E-mail cover letter and curriculum vitae with 3 references (names and email addresses / phone numbers) by on or before 2nd May 2026 to molly.j@sjri.res.in & cc to hr@sjri.res.in
Technical Support : Apply here
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