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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. यह भती स्क्लननकल िेवलपमेंट सववसम जे एजेंसी (CDSA) कें द्र में पररयोजना पदों की ररस्क्तयों को भरन े के सलए की जा रही है। CDSA, THSTI का एक ववशेष कें द्र है, स्जसे सावजम ननक स्वास््य रोिों के सलए ककफायती स्वास््य उत्पादों के ववकास को सुववधाजनक बनान े के उद्देवय स े स्थावपत ककया िया है। यह देश का एकमात्र सावजम ननक कें द्र है स्जसे लाभ-न कमान े वाल े तकनीक-आधाररत प्रीस्क्लननकल और स्क्लननकल उत्पाद ववकास के साथ-साथ सावजम ननक एजेंससयों द्वारा ककए जाने वाल े स्क्लननकल अनुसंधान को समथनम और पोषण देने के उद्देवय से बनाया िया है। यह प्रसशिण और सीखने के एक इको-ससस्टम के ववकास की ददशा में काम करता है और सावजम ननक िेत्र की संस्थाओ ं तथा छोटे और मध्यम उद्यमों (SME) के साथ समलकर नवाचारपणू म तकनीकों को जनदहत में गचककत्सीय उत्पादों में बदलन े का काय म करता है। 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 के मुख्य उद्िेश्य ननम्नलिखिर्त हैं: a. एक अकादसमक स्क्लननकल ररसच म यूननट के रूप में, अध्ययन योजना, सेटअप, सचं ालन, पररयोजना प्रबंधन, ननिरानी, िेटा प्रबंधन, सुरिा ररपोदटिंि, वववलेषण और ररपोटम लेखन में अन्वेषकों और SMEs को अंत-to-अंत स्क्लननकल अध्ययन समथनम प्रदान करना। b. स्क्लननकल ववकास/प्रयोजन और ननयमन के िेत्र में उच्च िुणवत्ता वाल े प्रसशिण के माध्यम स े शोध िमता और िमता का ननमाणम करना। c. देश में स्क्लननकल ररसच म पयामवरण का समथनम और सुदृढ करना। d. ननयामक ववज्ञान और नीनत समथनम : शोधकतामओ,ं ननयामकों, स्वास््य नीनत ननमामताओं और उद्योि को समथनम देने के सलए उपकरण और दृस्ष्ट्टकोण प्रदान करना। 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. यह भती ननम्नसलणखत पररयोजनाओं के तहत ब्रिक-टीएचएसटीआई की ररस्क्तयों को भरने के सलए है: This recruitment is to fill up the vacancies of BRIC-THSTI under the following projects:

पि के लिए आवश्यक शैक्षिक योग्यर्त और अनुभव /Educational Qualification and Experience required for the post: 1. पि क न म/Name of the पररयोजना प्रबंधक (ननरीिण )/Project Manager (Monitoring) post 01 पिों की सख्ं य /Number of the post Efficacy. Safety, and Tolerability of Ayurveda regimen as an adjunct to anti- पररयोजन क न म/Name tuberculosis treatment (ATT) and macronutrient supplementation on body of the Project 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 Rs. 78,000/- + HRA वेर्तन/Emoluments Up to 45 years उम्र/Age न्यनू र्तम शैक्षिक योग्यर्त Essential qualifications and work experience: और अनुभव/Minimum • Post Graduate Degree, including the integrated PG degrees, in any branch Educational of Life Sciences with five (5) years’ post qualification experience in clinical Qualification and trial monitoring. Experience OR • PhD in any branch of Life Sciences with two (2) years post qualification experience in clinical trial monitoring. Desirable qualifications and work experience: • Experience of clinical trial or public health project management in a recognised organisation/institute (academic clinical trials unit, CRO, pharmaceutical, biotechnology, or device company). • Demonstrable experience of line management, project management concepts, and ability to understand, explain and communicate project concepts using standard tools and templates The Project Manager (Monitoring) will be responsible for ensuring the quality, नौकरी क प्रोफ इि/ integrity, and compliance of assigned clinical research studies through robust Job profile monitoring and oversight activities. The role focuses on clinical site monitoring, quality assurance, risk-based oversight, and capacity building, while working in close coordination with the central study, regulatory, and project management. Key Responsibilities: Clinical Monitoring & Oversight • Conduct site qualification, initiation, routine monitoring, and close-out visits for assigned clinical research studies in accordance with approved monitoring plans. • Perform both onsite and remote monitoring to ensure subject safety, protocol adherence, data accuracy, and documentation completeness. • Review source documents, CRFs, informed consent forms, and essential documents to ensure compliance with protocol, GCP, and applicable regulations. • Identify, document, and follow up on protocol deviations, non-compliance issues, and data discrepancies. • Ensure timely preparation and submission of monitoring visit reports and follow-up letters.

Quality Assurance & Compliance • Support implementation and maintenance of quality management systems related to clinical monitoring and study oversight. • Ensure adherence to ICH-GCP, Indian regulatory requirements, ethics committee approvals, and institutional SOPs during study conduct. • Support audit and inspection readiness, including participation in audits and follow-up on assigned Corrective and Preventive Actions (CAPAs). • Contribute to the development and periodic review of monitoring plans, SOPs, checklists, and quality tools. Risk-Based Monitoring • Support the development and implementation of risk-based monitoring strategies. • Proactively identify study and site-level risks related to data quality, participant safety, or compliance. • Escalate critical issues to the study leadership and Quality/CPM teams in a timely and documented manner. Training & Capacity Building • Deliver GCP, GDocP and monitoring-related training to site staff and study teams as required. • Provide ongoing guidance and mentoring to site personnel to improve compliance, documentation quality, and operational performance. • Serve as a trainer for clinical research and monitoring-related training initiatives conducted by CDSA, as assigned. Coordination & Reporting • Work closely with the central study team, data management team, and Quality/CPM leadership to ensure effective study oversight. • Participate in internal study review meetings to provide updates on monitoring findings, site performance, and quality trends. • Maintain accurate and inspection-ready documentation of all monitoring and quality oversight activities. Travel Requirement • Must be willing to travel extensively to clinical sites across India, including short-notice travel and extended site visits when required. /Skills • Strong understanding of clinical trial monitoring, GCP, and human subject कौशि protection. • Demonstrated ability to independently manage assigned monitoring responsibilities with minimal supervision. • Strong observational, analytical, and problem-solving skills. • Excellent written and verbal communication skills in English. • Ability to prepare clear and concise monitoring reports, quality summaries, and follow-up documentation. • Proficient in MS Word, Excel, PowerPoint, and electronic clinical trial systems (EDC, CTMS, eTMF – as applicable). • Professional judgment, integrity, and the ability to build trust with investigators and site teams. • Ability to work collaboratively within multidisciplinary research teams. वॉक-इन इंिरव्य ू की नर्तधि/ Date 28th October 2026 @09:00 AM at THSTI, NCR Biotech Science Cluster, 3rd Milestone, Faridabad-Gurugram Expressway, Faridabad – 121001 of walk-in interview

नोि/ NOTE:- 1) The candidates must bring their latest CV/resume, one set of photocopy of documents in support of their educational qualification and experience, along with their originals and a valid ID card for verification. 2) Candidates coming after the time slot mentioned will not be entertained. 3) All the candidates coming for written test/skill test/interview at THSTI are mandatorily required to deposit their mobile phone along with valid Identity proof at the reception and the same will only be returned back on completion of the entire selection process. स म न्य ननयम व शर्त/ें GENERAL TERMS & CONDITIONS: a) These are the short-term positions, and extension will be granted subject to satisfactory performance of the incumbents and tenure of the project for which they are selected. Those appointed to these positions will not have any claim for regularization of their employment. a) All educational, professional and technical qualifications should be from a recognized Board/University. b) The experience requirement specified above shall be the experience acquired after obtaining the minimum educational qualifications specified for the post. The candidates are required to satisfy themselves, before applying /appearing for the selection process, that they possess the minimum eligibility criteria as laid down in the recruitment advertisement. No query will be entertained with regard to eligibility criteria. c) The date of Interview of the respective post will be the CRUCIAL DATE for determining eligibility with regard to age, experience, essential qualification etc. d) Age and other relaxations for direct recruits and departmental candidates: 1. By five years for candidates belonging to SC/ST communities. 2. By three years for candidates belonging to OBC communities. 3. For Persons with Benchmark Disabilities (PwBD) falling under the following categories: (i) UR - ten years, ii) OBC - 13 years (iii) SC/ST - 15 4. Age is relaxable for Central Government servants up to five years in accordance with the instructions or orders issued by the Central Government, from time-to-time. 5. Institute/Department employees will get the age relaxation to the extent of the service rendered by them as on closing date of advertisement. 6. For Ex-servicemen upto the extent of service rendered in defense forces (Army, Navy & Air force) plus 3 years provided they have put in a minimum of 6 months attested service. e) All results/notifications will only be published on our website. Therefore, the candidates should essentially visit THSTI website, regularly. f) All communications will only be made through email. g) In case many candidates appear for the walk-in interview, screening will be done to limit the number of candidates to those possessing higher/relevant qualification and experience. h) The no. of vacancy indicated above may change subjected to the actual requirement at the time of Written test/skill test/interview. i) With regard to any ...

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Applications are invited from the eligible candidates for the position of Project Associate-I (No-01), Project Associate-II (No-01) in the project "Inter-Institutional Programme for Maternal Neonatal and Infant Sciences a Translational approach-interdisciplinary group for advanced research on Birth outcomes-DBT India Initiative (GARBH-Ini Phase II)" of Funding Agency-DBT. PI- Prof. Arindam Maitra and Co-PI- Dr. Souvik Mukherjee