Pharm'Up 
The Clinical Development Services Agency (CDSA), a niche center of THSTI, is dedicated to facilitating the development of affordable healthcare products and supporting high-quality clinical research. CDSA is recruiting for multiple project positions for the BRIC-THSTI under the project titled: “INDIGO Effective and Affordable flu Vaccine for the world.”
Walk-in Interview Schedule & Venue
| Post Title | Number of Posts | Emoluments (Rs. + HRA) | Walk-in Date |
| Data Manager | 01 | ₹67,000/- | November 26, 2025 |
| Sr. Project Associate | 01 | ₹42,000/- | December 1, 2025 |
| Principal Project Associate | 01 | ₹49,000/- | December 1, 2025 |
- Time: 09:00 AM
- Venue: THSTI, NCR Biotech Science Cluster, 3rd Milestone, Faridabad-Gurugram Expressway, Faridabad – 121001.
Detailed Post Requirements
1. Sr. Project Associate (01 Post)
- Age Limit: 35 years.
- Minimum Educational Qualification & Experience:
- Professional degree (MBBS, BDS, BVSc, BAMS, BHMS, BUMS, BSMS, BNYS, B.Sc. Nursing, BPT, B.Pharm) with a minimum of one year of experience in clinical research. OR
- Graduate degree (3-year course) in Life Sciences with a minimum of two years of experience in clinical research. OR
- Postgraduate or PhD in Life Sciences with a minimum of one year of experience in clinical research.
- Mandatory: Good Clinical Practice (GCP) certification is compulsory.
- Job Profile: Supports all stages of clinical trials, manages regulatory documentation, leads Trial Master File (TMF) setup and maintenance, coordinates supplies, and performs periodic TMF quality control checks.
2. Principal Project Associate (01 Post)
- Age Limit: 35 years.
- Minimum Educational Qualification & Experience:
- Master’s degree/diploma in Life Sciences, Pharmacy, Public Health, or related discipline with a minimum of 2 years of relevant clinical trial monitoring or clinical trial/study coordinator experience. OR
- Bachelor’s in medical sciences with a minimum of three years of relevant experience.
- Job Profile: Functions as a Clinical Research Associate (CRA), performs site monitoring visits (initiation to closeout), ensures adherence to GCP/GCLP, manages documentation, and verifies data integrity (Source Data Verification/SDV).
3. Data Manager (01 Post)
- Age Limit: 40 years.
- Minimum Educational Qualification & Experience:
- Master’s degree in any field (preferably Science) with 6 years of post-qualification experience in clinical data management/clinical research/MIS/data analysis/IT. OR
- Graduation degree in any field (preferably Science) with 8 years of post-qualification experience in clinical data management/clinical research/MIS/data analysis/IT.
- Desirable: Diploma in Clinical research/data management, familiarity with industry-standard CDMS, and programming skills.
- Job Profile: Responsible for the preparation of Data Management documents (DMP, DVP, Annotated CRF), overseeing clinical database setup, ensuring compliance with standards like CDISC, SDTM, reconciling AE/SAE data, and managing query resolution and data cleaning.
General Terms
- The positions are temporary and co-terminus with the project.
- Closing date of the online application will be the CRUCIAL DATE for determining eligibility regarding age, essential qualification, and experience.
- Experience specified must be acquired after obtaining the minimum essential educational qualification.
- All communications will only be made through email and notifications on the THSTI website.
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