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Quality Control, Pharma Industry, R and D, CSIR, Food Industry, Pathology, Medical Writing, coding

Required Junior Research Fellow - B.S. 4 years programme/BPharm/MBBS/Integrated BS-MS/MSc/BE/BTech or equivalent degree, with 55% marks and passing of NET/GATE test- Fellowship Junior Research Fellow (JRF)- Rs.37,000/-p.m.

Nirma University, Institute of Science is hiring Junior Research Fellow  ADVERTISEMENT FOR JRF POSITION Date: 02/05/2026 Applications are invited from interested and motivated candidates for the post of Junior Research Fellow (IRF) in a time-bound research project under CSIR-HRDG sponsored research support scheme [project file no: 37WS (0038)-2023-24/EMR-IL/ASPIRE] for a temporary period, purely on a contractual basis as per the following details 1. Position: Junior Research Fellow (JRF) 2. Number of Vacancy: 01 3. Project Title: Profiling of interferon-alpha for early detection of maternal anaemia during pregnancy 4. Principal Investigator: Dr. Aarthi Sundararajan Assistant Professor Institute of Science, Nirma University Ahmedabad-382481 5. Department: Institute of Science  6. Project Tenure : 15 Months  7. Job Description: JRF responsibilities will include conducting research activities, maintaining proper data records, keeping track of consumables, assisti...
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Syenergen Bio Private Limited Requires Research Associate ( Report Writers ) - B. Pharm, M. Pharm. M Sc.

Syenergen Bio Private Limited Requires Research Associate ( Report Writers ) - B. Pharm, M. Pharm. M Sc. 
Details are provided below 
1. Post - Research Associate ( Report Writers) 
2. Company- Synergen Bio Private Limited Pune 
3. Department- Project Management and Biopharmaceutics 
4. Qualification- B  Pharm,  M. Pharm, M. Sc. 
5. No. Of Vacancies 02 
6. Experience- 1.5 + Years 
7. Note - Immediate Joiners preferred 
8. Job Location- Shivajinagar , Wakdewadi , Pune 
9. Tasks Responsibilities- 
a. Preparation of Clinical Study Report ( CSR) within proposed time line according to raw data and as per the regulatory requirements.  
b. Preparation of electronic copy of final reports ( scanning , book marking , hypertext linking , inherit zoom and creating TOC to PDFs 
c. Know about eCTD specifications guidelines for regulatory submissions 
d.  Coordination with Clinical, Bioanalytical department and principal and investigators while preparation of Clinical Study Report and compilation of data .
e. Data uploading ( demographies, Clinical laboratory values , vital signs , meal distribution, and Deviation of sample time point.) 
f. Preparation of relevant report appendices as per project.  
g. Coordinating with different sections with projects related activities.  
h. Preparation of regulatory summary reports in Module 02 and clinical study reports in Module 05( i e. eCTD Format) 
10. Interested candidates share CV on careers@synergenbio.com 
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