Project Technical Support-III (Social Worker)-ICMR ENT CBR Project SJRI | St. Johns Research Institute Job Opportunities Project Technical Support-III (Social Worker)-ICMR ENT CBR Project Non Division User Project / Title ICMR ENT CBR Project Contact Person Contact No 080497011/7021 Job Details Brief Description about the Project ICMR funded project on Community based model for Early detection - Speech and language training of hearing impaired children - Mixed methods Implementation study Project Technical Support-III (Social Worker) Position Starting: No. of Vacancy: One Preferred Qualifications: BSW / MSW ( Community Development specialisation preferred) Maximum Age Limit Salary: Rs 36,400/- Consolidated (Rupees thirty six thousand four hundred only including HRA) (This includes all expenses like statutory deductions etc.) Last Day for Receiving Application: 15th June 2025 Roles and Responsibilities : Conduct in depth interviews and focus group discussions Translation and preparation of transcripts from local language to English

Project Research Scientist-III (Non Medical) Position Starting: No. of Vacancy: Preferred Qualifications: Ph D (Social work with Community Development specialisation) Maximum Age Limit Salary: Rs 1,01,400/- Consolidated (Rupees One lakh one thousand four hundred only) including HRA, (This includes all expenses like statutory deductions etc.) Experience: Post Ph.D experience of 10 years with experience of co-ordinating community based research projects Last Day for Receiving Application: 15th June 2025 Roles and Responsibilities : Take complete responsibility for co-ordinating all field activities and report to the principal investigator - Prepare reports for monthly appraisal - Ensure quality of data collection and data entry -Training field staff to administer questionnaire and community based work

Project Technical Support-II (Social Worker)-ICMR ENT CBR Project SJRI | St. Johns Research Institute Job Opportunities Project Technical Support-II (Social Worker)-ICMR ENT CBR Project Non Division User Project / Title ICMR ENT CBR Project Contact Person Contact No 080497011/7021 Job Details Brief Description about the Project ICMR funded project on Community based model for Early detection - Speech and language training of hearing impaired children - Mixed methods Implementation study Project Technical Support-II (Social Worker) Position Starting: No. of Vacancy: Preferred Qualifications: Minimum qualification is PUC (passed).Social Work Graduates with community experience will be preferred. Maximum Age Limit Salary: Rs 26,000/- Consolidated (Rupees twenty six thousand only including HRA) (This includes all expenses like statutory deductions etc.) Last Day for Receiving Application: 15th June 2025 Roles and Responsibilities : Anganwadi visits and interviewing study respondents. - Scheduling follow up visits - Follow up of respondents with hearing problems and referral to project team

Vitamin D intervention trial during pregnancy. The pregnant women attending the OPD at St John s medical college hospital will receive 2 different dosage of Vitamin D supplement. To evaluate whether a daily supplement of an effective dose of 2000 IU/d vitamin D3 reduces the incidence of preterm births when compared to the pregnant women supplemented with the standard care 500 IU/d vitamin D3. They will be followed up during pregnancy for outcome measure such as preterm. No. of Vacancy: Preferred Qualifications: Experience: Minimum Experience: Fresher / with one year of experience, Maximum Experience: 2-3 Years experience in Research Last Day for Receiving Application: 25th May, 2025 Roles and Responsibilities : Recruitment of study participants Data collection and follow up until the study period. Handing over supplement Reporting day-to-day activities to the study JRF & PI.

Preferred Qualifications: MBBS/ NURSING/BDS with MPH or Masters in relevant field with experience in Maternal and Child health. Last Day for Receiving Application: Roles and Responsibilities: For oversight and overall coordination of the technical aspects of the project along with the research team including periodic monitoring of research activities of the implementation research projects To provide support and assist in the training of research project assistants, plan, organize, and implement health programs, and complement clinical work of the Neonatal Unit Leadership, capacity building, and mentoring of research health personnel and project assistants. Annual reports of the project in collaboration with the PI. Plan and develop research proposals, conduct research, and publish the results of the research..

Vitamin D intervention trial during pregnancy. The pregnant women attending the OPD at St John s medical college hospital will receive 2 different dosage of Vitamin D supplement. To evaluate whether a daily supplement of an effective dose of 2000 IU/d vitamin D3 reduces the incidence of preterm births when compared to the pregnant women supplemented with the standard care 500 IU/d vitamin D3. They will be followed up during pregnancy for outcome measure such as preterm. No. of Vacancy: Preferred Qualifications: MSc. Data Sciences / life sciences Language : English , Kannada , Tamil (optional), Hindi (optional) Experience: Minimum Experience: Fresher / with one year of experience, Maximum Experience: 2-3 Years experience in Research Last Day for Receiving Application: 25th May, 2025 Roles and Responsibilities : Recruitment of study participants Collect, clean, process, and manage dataset from various sources Stay updated on new methods and tools in data science relevant to public health and biomedical research. Ensure data integrity, security, and compliance with regulatory standards. Channelizing the study protocol with other team members for completion of study. Reporting day-to-day activities to the study PI.

Interaction with Patients, Sponsor/CRO, IEC, Lab staff and other departments in the institution and conduct the study according to ICH GCP Guidelines, SOPs and study protocol guidelines and act as the main line of communication between patients, Investigators and CROs in study conduct activities. Assist in Feasibility questionnaires, Coordinate in pre-site selection visit, site initiation visit. Assist the Principal Investigator and Co investigators in screening of subjects by maintaining and updating the list of potentially eligible patients for the ongoing studies Clinical Research Co-ordinator No. of Vacancy: Salary: 20,000/ month to be escalated depending on job performance English, Kannada and Hindi, Telugu 0 -1 year Preferred Qualifications: Degree with life Science background, trained in Clinical research e.g. Diploma in clinical research , or MSC Clinical research and Pharm D Minimum Experience : No. required: fresher Maximum Experience * No. required: 1 year Last Day for Receiving Application: Roles Responsibilities: Coordinate in screening, Audio-Video consenting, enrolment, periodic study visits and close out visit. Ensure that rights and well-being of a research participant is protected throughout the duration of the study. Coordinate with finance, legal and regulatory team and assist in the preparation of CTAs specific to the trials. Assure all study documentation is maintained by completing the source documents for each Patient and maintaining and updating Site Master Files. Completing CRFs, e-CRFs on time and resolve data queries. EDC, Inform & Medidata data capture. 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, AEs 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, DCGI and FDA queries. Coordinate and participate in monitoring visits with sponsor/CRO and Facilitating inspections/audits. Follow up with patients and document in telephone contact report. Conduct study closeout visit and archive the documents. Maintain record of closeout studies and resolve the post closeout queries. GC-P/C-IRMS, Orbitrap-MS) and IR spectroscopy (FTIR) for the ongoing research project.