RECRUITMENT NOTICE NO.: THS-C/RN/12/2026 Dated: 12
th May 2026
RECRUITMENT NOTIFICATION
1. BRIC-Translational Health Science and Technology Institute (THSTI) is an Institute of the Biotechnology
Research and Innovation Council, Department of Biotechnology, Ministry of Science & Technology, Govt.
of India. The institute is an integral part of the interdisciplinary NCR Biotech Science Cluster located at
Faridabad, with the mission to conduct innovative translational research and to develop research
collaborations across disciplines and professions to translate concepts into products to improve human
health.
2. BRIC-THSTI has built several inter-institutional collaborations and connectivity with industry supported
by well-trained teams of research and laboratory staff. THSTI has established various centres namely
(a)
Centre for Maternal and Child Health,
(b) Centre for Virus Research, Therapeutics and Vaccines
(c) Centre
for Tuberculosis Research
(d) Centre for Microbial Research,
(e) Centre for Immunobiology and
Immunotherapy
(f) Centre for Drug Discovery
(g) Clinical Development Services Agency
(h)
Computational and Mathematical Biology Centre
(i) Centre for Bio-design and Diagnostics.
These centres
are strengthened by many core facilities viz. Bioassay Laboratory, Biorepository, Biosafety Level-3 Lab,
Data Management Centre, Immunology Core laboratory, Multi-Omics facility, Experimental Animal Facility,
Vaccine design and Development facility, School of Innovation in Bio design etc. that serve as huge
resources for the research programmes of THSTI and also the National Capital Region Biotech Science
Cluster and other academic and industrial partners. BRIC-THSTI trains the next generation of scientific
leaders through many ambitious and globally competitive academic courses which promotes research and
innovation through multi-disciplinary academia-industry partnerships.
3. This recruitment is to fill up the vacancies for project positions at Clinical Development Services Agency
(CDSA) center. CDSA is a niche center of THSTI established to facilitate development of affordable
healthcare products for public health diseases. It is the only public Centre in the country created with
a mandate to support and nurture cost-effective, high quality, not-for-profit technology-based
preclinical and clinical product development as well as support clinical research conducted by public
agencies. It works towards development of an eco-system for training and learning and work with
public sector institutions, and small and medium enterprises (SME) to translate innovative technologies
into medical products for public good.
CDSA The main objectives of CDSA are:
a. As an academic Clinical Research Unit, to undertake & provide end -to- end clinical study
support for investigators and SMEs in study planning, set up, conduct: project management,
monitoring, data management, safety reporting, analysis and report writing
b. Build research capacity and capability through high quality training in the area of clinical
development/trials and regulation
c. Support and strengthen clinical research environment in the country
d. Regulatory science and policy support: provide tools and approaches to support researchers,
regulators, health policy makers & industry.
4. This recruitment is to fill up the vacancies of BRIC-THSTI under the following projects:
Educational Qualification and Experience required for
the post:
1. Name of
the post Research Officer
Name of the
Project
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
Emoluments Rs. 67,000/- + HRA
Age 40 years
Minnimum
Educational Qualification
and Experience
• Post Graduate Degree, including the integrated PG degrees, in any branch
of Life Sciences with three (3) years post qualification experience in clinical
trial monitoring.
OR
• PhD with experience in clinical trial monitoring.
Job profile
The Research Officer plays a pivotal role in supporting the execution and
management of clinical trials across all stages. Working under the direction of
the Project Manager and study monitors, they ensure the smooth operation
of daily trial activities, maintain regulatory and trial documentation, and
coordinate communication and logistics across study stakeholders. This role is
expected to work independently on assigned tasks, proactively identify
potential issues, and propose process improvements.
Key Responsibilities:
Clinical Trial Support & Documentation
• Coordinate and track the distribution and reconciliation of clinical trial
supplies, laboratory kits, and investigational products to investigational
sites.
• Ensure timely delivery and tracking of essential study documents and
materials in accordance with study timelines and site activation plans.
• Maintain and regularly update trial tracking tools (e.g., enrollment logs,
regulatory document trackers, training logs).
Regulatory & Site Start-up Support
• Support CRAs and site staff in the collection, review, and tracking of
essential regulatory documents for ethics committee and regulatory
authority submissions.
• Assist in preparing site initiation packages and supporting site readiness for
activation.
• Liaise with regulatory, legal, and contracts departments to ensure timely
processing of site contracts and confidentiality agreements.
Trial Master File (TMF) Oversight
• Lead TMF set-up and ongoing maintenance, ensuring completeness,
accuracy, and audit-readiness of clinical documentation.
• Perform periodic TMF quality control (QC) checks and contribute to TMF
metrics and reconciliation activities.
• Support the development and implementation of TMF filing plans and
oversight reports.
Meeting Coordination & Communication
• Schedule, coordinate, and document clinical team meetings, site
communications, and teleconferences; maintain meeting agendas and
minutes.
• Assist with the organization and execution of investigator meetings,
including logistics, preparation of materials, and follow-up documentation.
Data & Site Management
• Support CRAs with clinical data flow, Case Report Form (CRF) tracking, and
resolution of data queries with investigational sites.
• May accompany CRAs on monitoring visits to gain on-site experience and
provide additional support during critical phases of the trial.
Cross-functional & Operational Support
• Serve as the central point of contact for the clinical team regarding projectspecific communications and documentation.
• Collaborate with Clinical Portfolio Management, Regulatory Affairs, Data
Management, and Quality Assurance to ensure alignment of deliverables.
• Support budget tracking, invoice verification, and financial documentation
coordination related to trial expenses and vendor contracts.
Quality & Compliance
• Ensure adherence to ICH-GCP, applicable regulatory requirements, and
internal Standard Operating Procedures (SOPs).
• Participate in internal and external audits and inspections as needed;
support audit readiness and CAPA (Corrective and Preventive Action)
implementation.
• Contribute to internal quality initiatives and process optimization efforts.
Skills
• Strong understanding of ICH-GCP guidelines and clinical trial lifecycle.
• Experience working with electronic Trial Master File (eTMF), Clinical Trial
Management Systems (CTMS), and document management platforms.
• Excellent communication, organizational, and problem-solving skills.
• Detail-oriented with the ability to manage multiple tasks and prioritize
effectively.
• Proficient in MS Office Suite (Word, Excel, PowerPoint, Outlook).
Date of walk-in interview for
Sr. No. 1:
25th May 2026 @ 09:00 AM at THSTI, NCR Biotech Science Cluster,
3rd Milestone, Faridabad-Gurugram Expressway, Faridabad – 121001
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