The Translational Health Science and Technology Institute, an autonomous institute of the Department of Biotechnology based in Faridabad, Haryana, is hiring for the Project Manager (Monitoring) post on a contract basis, with one vacancy on offer. The position falls under the institute's Clinical Development Services Agency and relates to a clinical study on tuberculosis treatment, involving site monitoring, quality assurance and oversight of clinical research across India.
THSTI Project Manager Recruitment 2026
- Notification09 Oct
- Walk-in28 Oct
THSTI Project Manager Recruitment 2026
Job Overview
- Organization
- Translational Health Science and Technology Institute
- Advertisement No.
- THS-C/RN/19/2026
- Post Name
- Project Manager (Monitoring)
- Job Location
- Faridabad, Haryana
- Who Can Apply
- Candidates from anywhere in India
- Job Type
- Contract
- Age Limit
- Up to 45 years
- Gender
- All
- Nationality
- Indian
- Experience
- Five years post qualification experience in clinical trial monitoring with a Post Graduate Degree, or two years post qualification experience in clinical trial monitoring with a PhD
- Pay Scale
- Rs. 78,000/- + HRA
- Tenure
- Short-term project position; extension subject to satisfactory performance and the tenure of the project
Vacancy Breakdown
| Post Name | Total |
|---|---|
| Project Manager (Monitoring) | 1 |
Eligibility Details
Post Graduate Degree, including the integrated PG degrees, in any branch of Life Sciences with five (5) years post qualification experience in clinical trial monitoring. OR PhD in any branch of Life Sciences with two (2) years post qualification experience in clinical trial monitoring. Desirable: 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.
| Post | Qualification |
|---|---|
| Project Manager (Monitoring) - Qualification and Experience | Post Graduate Degree, including the integrated PG degrees, in any branch of Life Sciences with five (5) years post qualification experience in clinical trial monitoring. OR PhD in any branch of Life Sciences with two (2) years post qualification experience in clinical trial monitoring. Desirable: 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. |
Age Limit
Up to 45 years as on the date of interview
Age Relaxation
5 years for SC/ST, 3 years for OBC, PwBD 10 years (UR), 13 years (OBC), 15 years (SC/ST), Central Government servants up to 5 years, Institute/Department employees to the extent of service rendered, Ex-servicemen up to service rendered in the defence forces plus 3 years with a minimum of 6 months attested service
Selection Process
- 1Walk-in Interview
Candidates report at the THSTI Faridabad campus at 09:00 AM; if a large number of candidates appear, screening is done to limit the number to those with higher or relevant qualification and experience.
Salary Structure
Rs. 78,000/- + HRA
How to Apply
- 1Reach the THSTI campus at NCR Biotech Science Cluster, 3rd Milestone, Faridabad-Gurugram Expressway, Faridabad 121001 by 09:00 AM.
- 2Carry the latest CV or resume and one set of photocopies of documents supporting your educational qualification and experience.
- 3Bring the original documents and a valid ID card for verification.
- 4Deposit your mobile phone and valid identity proof at the reception on arrival; they are returned only after the entire selection process is complete.
Reporting Venue
THSTI, NCR Biotech Science Cluster, 3rd Milestone, Faridabad-Gurugram Expressway, Faridabad 121001
Reporting time: 09:00 AM
Candidates must arrive by 09:00 AM at the venue; those coming after the time slot will not be entertained. Mobile phones and a valid identity proof must be deposited at the reception on arrival and are returned only after the entire selection process is complete. If many candidates turn up, screening will be done to limit the number to those with higher or relevant qualification and experience.
Documents to Carry / Upload
Important Details
- These are short-term project positions under the CDSA centre; extension is subject to satisfactory performance of the incumbent and the tenure of the project, and appointees will have no claim for regularization of employment.
- The date of interview is the crucial date for determining age, experience and essential qualification.
- The post requires extensive travel to clinical sites across India, including short-notice travel and extended site visits.
Project
Efficacy, Safety, and Tolerability of Ayurveda regimen as an adjunct to anti-tuberculosis 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.
Job Profile
The Project Manager (Monitoring) ensures the quality, integrity and compliance of assigned clinical research studies through monitoring and oversight. Duties cover site qualification, initiation, routine monitoring and close-out visits, onsite and remote monitoring, review of source documents, CRFs, informed consent forms and essential documents, follow-up on protocol deviations and data discrepancies, monitoring visit reports, quality management systems, ICH-GCP and regulatory compliance, audit and inspection readiness including CAPAs, risk-based monitoring, GCP and GDocP training for site staff, and coordination with the central study, data management and Quality/CPM teams.
Key Skills
- Strong understanding of clinical trial monitoring, GCP and human subject protection.
- 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).
- Professional judgment, integrity and ability to build trust with investigators and site teams.
- Ability to work collaboratively within multidisciplinary research teams.
Frequently Asked Questions
How will candidates be informed about results and further updates?
All results and notifications are published only on the THSTI website, and all communication is made through email.
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