CDSA (THSTI) Walk-In Interview for Clinical Research Roles: Focus on Maternal & Neonatal Outcomes

The Clinical Development Services Agency (CDSA), a niche center of the Translational Health Science and Technology Institute (THSTI) under the Department of Biotechnology (DBT), is holding a walk-in selection process to fill temporary project positions.

The recruitment is for the project titled “Improving maternal and neonatal outcomes using imaging data science.” CDSA’s mission is to facilitate the development of affordable, high-quality healthcare products and support clinical research for public health.

Available Positions and Emoluments

Post Name	No. of Posts	Fixed Emoluments (Per Month)	Upper Age Limit
Project Research Scientist – II (Non-Medical)	01	₹67,000/- + HRA	45 years
Project Technical Support – III	01	₹28,000/- + HRA	35 years

Note: The positions are short-term, contractual, and co-terminus with the project tenure. They do not confer any right to regular employment at THSTI/CDSA.

Detailed Eligibility and Job Profile

1. Project Research Scientist – II (Non-Medical)

This role functions as a Program Manager (Quality Monitoring), overseeing the operational and compliance aspects of assigned clinical studies.

Detail	Requirement
Essential Qualification	Master’s Degree/PG Diploma/PhD in Life Sciences / Biomedical Sciences / Pharmacy / Public Health / Clinical Research OR MBBS/BDS/BVSc.
Essential Experience	Minimum of five (5) years of experience in clinical project management and/or clinical trial/study monitoring in a recognized organization (CRO, pharma, academia, etc.).
Key Responsibilities	Overseeing and managing clinical trials, developing and maintaining project plans, managing budgets, conducting site qualification/monitoring visits (requires extensive travel), coordinating regulatory/ethics submissions, and ensuring adherence to GCP and regulatory requirements.

2. Project Technical Support – III

This role provides critical data and process monitoring support to the clinical trial team.

Detail	Requirement
Essential Qualification	Professional degree in B.Pharm (or MBBS, BDS, BVSc, BAMS, BHMS, BUMS, BSMS, BNYS, B.Sc. Nursing, BPT) OR Postgraduate or Ph.D. in Life Sciences OR Graduate degree (3 years) in Life Sciences with a minimum of 3 years of post-qualification experience in clinical research.
Mandatory	Good Clinical Practice (GCP) certification is required.
Key Responsibilities	Assisting with data and process monitoring, supporting co-monitoring visits (requires travel), maintaining the Trial Master File (TMF) and Investigator Site Files (ISF), assisting with regulatory/ethics submissions and documentation, and coordinating study logistics.

Walk-In Interview Details

Interested and eligible candidates must appear for the selection process in person.

Event	Details
Date of Selection	06th October 2025
Time	09:00 AM
Venue	THSTI, NCR Biotech Science Cluster, 3rd Milestone, Faridabad-Gurugram Expressway, Faridabad – 121001.

Note for Candidates:

Candidates must bring their latest resume, one set of photocopies of all educational qualification and experience documents along with the originals, and a valid ID card for verification.
Candidates arriving after the specified time slot will not be entertained.
All candidates must mandatorily deposit their mobile phone and a valid ID proof at the reception before the selection process.
The selection will be based on a written test/skill test/interview.