St. John’s is inviting applications for Project Technical Support II under the ICMR PANCREAS Study Project in Bangalore, Karnataka. The position involves clinical research coordination for an observational study examining the nutritional status of children with pancreatitis.
Freshers and candidates with 0–6 months of experience can apply. Eligible applicants should have a life sciences, nutrition, clinical research, or Pharm.D background and be familiar with clinical research documentation and ICH-GCP guidelines.
Job Details
| Particulars | Details |
|---|---|
| Organization | St. John’s |
| Project | ICMR PANCREAS Study Project |
| Job Title | Project Technical Support II |
| Job Location | Bangalore, Karnataka |
| Job Type | Contract |
| Experience | 0–6 months; freshers can apply |
| Monthly Salary | ₹26,000 |
| Total Vacancies | 1 |
| Tentative Joining Date | 15 October 2026 |
| Application Deadline | 4 October 2026 |
| Preferred Languages | English, Kannada, Telugu |
Number of Vacancies
There is 1 vacancy for the Project Technical Support II position under the ICMR PANCREAS Study Project.
Job Responsibilities
Selected candidates will support the Principal Investigator and Co-investigators in conducting the observational clinical study.
Key responsibilities include:
- Protecting the rights and well-being of research participants throughout the study.
- Screening potential participants and maintaining updated lists of eligible patients.
- Maintaining study documentation and completing source documents.
- Completing case report forms (CRFs) and electronic case report forms (e-CRFs) on time and resolving data queries.
- Performing electronic data capture using the REDCap database.
- Maintaining study consumables, investigational product accountability, storage, dispensing, temperature tracking, and equipment calibration.
- Coordinating sample centrifugation and the shipment of laboratory samples and study documents.
- Preparing, notifying, and tracking Institutional Ethics Committee (IEC) submissions.
- Submitting study progress reports, amendments, protocol deviations, adverse events (AEs), and serious adverse events (SAEs) to the ethics committee and sponsor on time.
- Coordinating with investigators and the safety monitoring team during SAEs.
- Assisting with the resolution of IEC queries.
- Following up with patients and documenting telephone contact reports.
- Conducting study closeout visits and archiving study documents.
Eligibility Criteria and Qualifications
Candidates should meet the following preferred qualification criteria:
- A degree in life sciences or nutrition.
- B.Sc. or M.Sc. in Clinical Research, or a Diploma in Clinical Research.
- Pharm.D candidates are also eligible.
- Freshers and candidates with 0–6 months of experience are welcome to apply.
The job description lists a maximum experience requirement of one year.
Required Skills
Candidates should have relevant knowledge or training in the following areas:
- Clinical research and ICH-GCP guidelines.
- Clinical study documentation and source data recording.
- CRF and e-CRF completion.
- Electronic data capture using REDCap.
- Ethics committee submissions and clinical study reporting.
- Patient follow-up and coordination with investigators and laboratory staff.
- English, Kannada, and Telugu language proficiency is preferred.
Application Process
Eligible candidates must email their cover letter and curriculum vitae (CV) along with details of three references.
Application deadline: 4 October 2026
Email your application to:
- To: shalini.h@sjri.res.in
- CC: hr@sjri.res.in
Include three references with their names and email addresses or phone numbers.