Life Sciences Research Jobs | THSTI Recruitment | Apply Now
Searching for prestigious government Research Jobs in biotechnology and clinical research? Here’s a massive opportunity for candidates passionate about building a Career in Life Sciences! Translational Health Science and Technology Institute has released THSTI Recruitment 2026 for multiple positions under its CDSA clinical research projects. Candidates with backgrounds in Life Sciences, Biotechnology, and Clinical Research can apply for highly rewarding project-based opportunities in clinical trial monitoring and translational research.
About the Institute
Translational Health Science and Technology Institute is an institute under the Biotechnology Research and Innovation Council (BRIC), Department of Biotechnology, Government of India. Located within the NCR Biotech Science Cluster, THSTI focuses on translational research aimed at improving human health. The institute has advanced centres dedicated to tuberculosis research, microbial research, immunology, vaccine development, bio-design, and computational biology. THSTI collaborates with academic institutions, healthcare organizations, and industries to develop innovative healthcare solutions and strengthen clinical research capabilities in India.
THS-C/RN/12/2026
1. Research Officer (01 Post)
- Project Title: Efficacy, Safety, and Tolerability of Ayurveda regimen as an adjunct to antituberculosis treatment (ATT) and macronutrient supplementation on body weight, nutritional outcomes, and quality of life in adults with newly diagnosed drug-sensitive NAAT-positive Pulmonary Tuberculosis: An open-label randomized controlled parallel-arm clinical study
- Qualification: Post Graduate Degree, including integrated PG degrees, in any branch of Life Sciences OR PhD in any branch of Life Sciences
- Experience: Minimum 3 years post-qualification experience in clinical trial monitoring for PG candidates. Experience in clinical trial monitoring for PhD candidates
- Key Responsibilities:
• Support execution and management of clinical trials across all stages
• Coordinate clinical trial supplies, laboratory kits, and investigational products
• Maintain trial tracking tools, regulatory documents, and training logs
• Assist in ethics and regulatory submissions and site start-up activities
• Manage and maintain Trial Master File (TMF) and perform QC checks
• Coordinate meetings, investigator communications, and documentation
• Support CRF tracking, data query resolution, and monitoring visits
• Collaborate with regulatory, quality, and project management teams
• Ensure compliance with ICH-GCP, SOPs, and regulatory requirements
• Support audits, inspections, CAPA implementation, and quality initiatives - Skills:
• Strong understanding of ICH-GCP guidelines and clinical trial lifecycle
• Experience with eTMF, CTMS, and document management platforms
• Excellent communication, organizational, and problem-solving skills
• Ability to manage multiple tasks effectively
• Proficiency in MS Office Suite - Emoluments: Rs. 67,000/- + HRA
- Age: 40 years
2. Clinical Research Associate (02 Posts)
- Project Title: Efficacy, Safety, and Tolerability of Ayurveda regimen as an adjunct to antituberculosis treatment (ATT) and macronutrient supplementation on body weight, nutritional outcomes, and quality of life in adults with newly diagnosed drug-sensitive NAAT-positive Pulmonary Tuberculosis: An open-label randomized controlled parallel-arm clinical study
- Qualification: Master’s degree in Life Sciences/ Health-related discipline
- Experience: Minimum 3 years of relevant clinical trial monitoring experience for Master’s degree holders.
- Key Responsibilities:
• Conduct site monitoring visits from initiation to closeout
• Ensure compliance with protocol, GCP, SOPs, and regulatory requirements
• Set up trial sites and manage investigational products and trial supplies
• Perform quality assurance checks as per GCP/GCLP standards
• Train and support site staff on trial procedures and protocols
• Maintain monitoring documentation, reports, and follow-up actions
• Track regulatory submissions, patient enrolment, CRF completion, and data queries
• Perform source data verification and ensure data accuracy
• Escalate protocol deviations and quality issues when required
• Collaborate with clinical operations, safety, regulatory, and data management teams
• Travel frequently to assigned study sites - Skills:
• Proficiency in Microsoft Office Suite
• Strong knowledge of ICH-GCP, GCLP, and regulatory guidelines
• Excellent documentation, communication, and organizational skills
• Strong time management and multitasking abilities
• Ability to travel frequently - Emoluments: Rs. 67,000/- + HRA
- Age: 40 years
3. Senior Project Associate (01 Post)
- Project Title: Efficacy, Safety, and Tolerability of Ayurveda regimen as an adjunct to antituberculosis treatment (ATT) and macronutrient supplementation on body weight, nutritional outcomes, and quality of life in adults with newly diagnosed drug-sensitive NAAT-positive Pulmonary Tuberculosis: An open-label randomized controlled parallel-arm clinical study
- Qualification: Post Graduate Degree, including integrated PG degrees, in any branch of Life Sciences with Good Clinical Practice (GCP) certification is mandatory
- Experience: Experience in clinical trial/site monitoring and clinical research activities
- Key Responsibilities:
• Conduct site monitoring visits from initiation to closeout
• Ensure trials are conducted as per protocol, SOPs, GCP, and regulatory requirements
• Perform quality functions across clinical operations and laboratories
• Set up trial sites and manage trial materials and supplies
• Provide protocol and trial training to site staff
• Maintain monitoring documentation, visit reports, and action plans
• Track regulatory approvals, recruitment, CRF completion, and data queries
• Perform source data verification and ensure data accuracy
• Archive and maintain trial documentation and correspondence
• Evaluate site quality and escalate issues to senior management
• Support Clinical Portfolio Management and internal departments as required - Skills:
• Strong understanding of ICH-GCP guidelines and clinical trial lifecycle
• Experience with eTMF, CTMS, and document management platforms
• Strong written and verbal communication skills
• Effective time management and multitasking abilities
• Proficiency in MS Office applications - Emoluments: Rs. 56,000/- + HRA
- Age: 35 years
How to Apply for these Research Jobs?
1. Eligible candidates can apply online through the official THSTI Recruitment Portal.
Last date to Apply: 01 June 2026.
2. Candidates applying for the Research Officer position must attend the walk-in interview with required documents.
Walk In Interview Details – Research Officer Position
- Date: 25 May 2026
- Time: 09:00 AM
- Venue: THSTI, NCR Biotech Science Cluster, Faridabad
General Terms & Conditions
- These are temporary project-based positions
- Experience should be post qualification
- Selection will be based on screening/interview
- Applications through any other mode will not be accepted
- Candidates must fulfill all eligibility criteria
- Age relaxation applicable as per Government of India norms
If you are searching for Research Jobs in biotechnology, clinical trials, or public health research, then THSTI Recruitment 2026 offers an exceptional Career in Life Sciences. With government-backed clinical research projects, strong research infrastructure, and high-impact healthcare programs, these opportunities can significantly strengthen your professional research career.
