Project Technical Support II _ ICMR PANCREAS Study Project

St John's; Bengaluru; On-site; INR 264,000 - 316,000; Part time

Job summary

St John's in Bengaluru is seeking a Contract Project Technical Support II for the ICMR PANCREAS Study. The role involves assisting the Principal Investigator in screening subjects and supervising protocol execution under ICH GCP guidelines.

The position requires 0-6 months of experience (freshers acceptable) and English/Kannada/Telugu language skills; tentative joining date is 15th October 2026. Salary offered is Rs. 26,000 per month.

Qualifications

• Degree with life science background and nutrition.
• Trained in clinical research (Diploma in clinical research or BSc/ MSc in clinical research, nutrition or Pharm D).

Responsibilities

• Protect rights and well-being of participants during the study.
• Maintain source documents for each subject and update eligibility lists.
• Complete CRFs/eCRFs on time and resolve data queries.
• Handle electronic data capture including REDCap database.
• Manage inventory of study consumables and product handling.
• Coordinate ethics submissions and track approvals with IEC/IRB.
• Communicate with investigators and safety monitoring teams during SAEs.
• Follow up with patients and document telephone contacts.
• Conduct study closeout visits and archive documents.

Education

Life science degree with nutrition

Diploma/BSC/MSC in clinical research (or Pharm D)

Job description

Project Technical Support II _ ICMR PANCREAS Study Project

Employment Type: Contract

Experience: 0-6 Months/ Freshers acceptable

Job Summary:

The study is an observational study on the nutritional status on children with pancreatitis. 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.

Salary : Rs. 26000/- p.m

Vacancy: One

Key Responsibilities:

• Ensure that rights and well-being of a research participant is protected throughout the duration of the study.
• Assure all study documentation is maintained by completing the source documents for each
• Completing CRFs, e-CRFs on time and resolve data queries.
• Electronic data capture including REDCAP database.
• 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.
• Timely preparation, notification and tracking of the Ethics committee submissions.
• Submission of the study progress, amendments, Protocol Deviations, AE's and SAEs to the ethics committee and sponsor in a timely manner.
• Coordinate with the investigator and the safety monitoring team at the time of SAEs.
• Assist in resolving IEC queries.
• Follow up with patients and document in telephone contact report.
• Conduct study closeout visit and archive the documents.

Eligibility Criteria:

Preferred Qualifications: Degree with life Science background, nutrition , trained inClinical research e.g. Diploma in clinical research, or BSC or MSC Clinical research, nutrition or Pharm D

• Maximum Experience * No. required: 1 year

Experience: 0-6 months, Freshers also acceptable

Preferred Language: English, Kannada, Telugu

Tentative Date of Joining : 15th October 2026