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 conducts innovative translational research and to develop research collaborations across disciplines and professions to translate concepts into products to improve human health.
This recruitment is to fill up the vacancies of BRIC-THSTI under the following projects
Project Scientist (Pharmacist) One post
Project : First-in-India Sham-Controlled Human Challenge Model Using Influenza Vaccines: A Catalyst for Early Clinical Validation of Novel Vaccines and Immunotherapies
Monthly consolidated emoluments : Rs. 75,000/-
Age Limit : 35 years
Essential & Desirable qualifications & Experience : M.Pharma from a recognized university with atleast one (1) years’ of post-qualification experience in clinical trial pharmacy. OR B.Pharma from a recognized university with atleast three (3) years’ of post-qualification experience in clinical trial pharmacy. The candidate must have a valid registration certificate from the State Pharmacy Council. The candidate must have a knowledge of drug storage and dispensing regulations.
Job description/ Skills required : • Understanding of establishing a sterile compounding pharmacy setting and GCP style documentation and traceability to support regulated Phase I human clinical trials.
• Manage the complex preparation of the Investigational Product (IP), often involving "Extemporaneous Preparation"
• Maintain the "Blinding" integrity of the study
• Work directly with the Dose Escalation Committee (DEC). Once a safety cohort is cleared, the pharmacist is responsible for calculating and preparing the next (higher) dose level for the subsequent cohort
• Ensure that high-precision analytical balances and laminar flow hoods are qualified (IQ/OQ/PQ) and calibrated
• Investigational product management (receipt, storage, dispensing, accountability)
• Temperature monitoring and maintenance of pharmacy logs
• Drug accountability and reconciliation
• Preparation and labeling as per protocol requirements
• Compliance with pharmacy regulations and GCP guidelines • Coordination with sponsor for drug supplies
• Support in sample processing and laboratory activities.
Date of walk-in interview : 5th May 2026
Project Assistant One post
Project : Development of monovalent and multivalent poultry vaccine using THSTI Multivalent self-assembled Nanocage Vaccine platform (MSN platform)
PI : Dr. Sweety Samal
Monthly consolidated emoluments : Rs. 35,000/-
Age Limit : 35 years
Essential & Desirable qualifications & Experience : Masters in any branch of Life Sciences from a recognized university with two (2) years’ of post-qualification experience in virology, molecular biology and immunology.
Job description/ Skills required : • Knowledge of virology, biochemistry, immunology and molecular biology related to cell culture, virus characterization, RT-PCR.
• Preference will be given to candidate having experience of handling human or animal viruses.
• Ability to perform physical tasks within a laboratory workspace and working experience in ABSL2 / ABSL3.
Date of walk-in interview : 8th May 2026
Data Manager One post
Project : A Study of Etiopathogenesis of Systemic Inflammation in Acute Pancreatitis, its Functional Consequences and Progression to Chronic Pancreatitis
PI : Dr. Nitya Wadhwa
Monthly consolidated emoluments : Rs. 56,000/- plus HRA
Age Limit : 35 years
Essential & Desirable qualifications & Experience : Masters’ degree in any field preferably in science, with six (6) years’ of post-qualification experience in clinical data management/ clinical research/ operations/ MIS/ data analysis/IT/ computer science/ healthcare field. OR Graduation degree in any field preferably in science, with eight (8) years’ of post-qualification experience in clinical data management/ clinical research/ operations/ MIS/ data analysis/IT/ computer science/ healthcare field.
Desirable : • Diploma in IT/ computer applications/ clinical data management.
• Familiarity with industry standard CDMS and some programming skills.
• Demonstrated experience of developing clinical study data management documents.
• Exposure to programming languages (Python, R) and data visualization tools (Tableau) will be an added advantage
Job description/ Skills required :
• Overall responsible for all data management activities of assigned project.
• Support the setting-up, maintenance, and closure of the data management aspects of the project. • Perform database testing and database audit as part of Quality Control.
• Prepare or perform review of Data Management documents - DMP (Data Management Plan), DVP (Data Validation Plan/ Edit Checks Document), Annotated CRF, Data Entry Guidelines etc.
• Working knowledge of query management, data cleaning, data freezing and data archival.
• Ensure accuracy, consistency, and completeness of the data for analysis.
• Prepare interim/ad-hoc reports and participating in data extraction collaboration with the stakeholders.
• Create data visuals (charts, graphs, dashboards, and other visual representations) in Tableau, Power BI, as required to present data.
• Coordinate with intra- or inter- departments to ensure all required, vital information and documentation is acquired in a timely manner.
• Participate in team meetings & external meetings as DM representative.
• Prepare data transfer guidelines for external data load and self- evident correction chart. • Ensure that data integrity and confidentiality of participants are protected
• Coordinate the archiving of study databases and related documents.
• Prepare interim reports for clinical study status and participating in data extraction in collaboration with the sponsor and coordinating site.
• Generate ad-hoc reports as needed
• Sound knowledge of logics and data management techniques
• Coordinate the archiving of study databases and related documents
• Develop standard operation procedures (SOPs) and working practice documents including the training of staff.
• Supervision of Data Management activities at sites.
Date of walk-in interview : 7th May 2026
Project Research Scientist-II (Synthetic Organic Chemist) One post
Project : Optimized salicylamide derivatives and prodrugs for the treatment of influenza infections
PI : Dr. Dinesh Mahajan
Monthly consolidated emoluments : Rs. 67,000/- plus HRA
Age Limit : 40 years
Essential & Desirable qualifications & Experience : Masters’ in Organic Chemistry from a recognised university/ Institute with four (4) years’ of post-qualification experience in synthetic organic chemistry.
Desirable:- A candidate with relevant experience in an industrial/ Pharma/ CRO/ biotech setup shall be preferred.
Job description/ Skills required : The incumbent is expected to work on synthetic organic chemistry projects in a time-bound manner at the Centre for Drug Discovery (CDD) at THSTI. The candidate with prior experience in synthetic organic chemistry, especially in photochemistry, electrochemistry, and/or organometallic chemistry, is preferred.
Date of walk-in interview : 4th May 2026
Project Research Scientist-III (Medical) One post
Project : Graded Risk-based Assessment for Screening and Prevention of Placental disorders (GRASPP) - A Randomized Controlled Trial Evaluating a Two-Step Contingent Screening Strategy for Great Obstetric Syndrome
PI : Dr. Nitya Wadhwa
Monthly consolidated emoluments : Rs. 93,000/- plus HRA
Age Limit : 45 years
Essential & Desirable qualifications & Experience : M.D./ MDS/ MPH/ Ph.D. orequivalent degree with basic degree as MBBS/ BDS from arecognized university, including the integrated PG degrees, withthree (3) years’ of post qualification experience in clinicalresearch.
Desirable :
• Experience in clinical research or related field.
• Good writing skills as well asverbal communication skills.
• Computer skills includingproficiency in use of Microsoft Office applications.
• Good organizational and problem-solving skills.
• Effective time management and ability to manage competing priorities.
Job description/ Skills required : The candidate selected for the said post will act as Clinical Research Coordinator (CRC) and will be leading the study team and will be primary point of contact for operational aspects of implementation of the clinical trial activities from study startup to completion of study, ensuring compliance with GCP and applicable guidance. CRC will be the primary link between study coordination unit and study investigators. CRC will be responsible for:
• Supervising all study site activities such as enrollment, consenting, administration of tests, CRF filling and training.
• Ensuring that study is conducted in accordance with study protocol, standard operating procedures, Good Clinical Practice, and applicable guidelines.
• Providing input and/ or developing study related material such as clinical operations plan, SOPs, CRF completion guidelines, informed consent, study logs/forms and other study related documents
• Supporting the submissions for relevant government/ ethics approvals
• Developing training module and planning the initial and retraining sessions for the research study staff along with the site CROs. • Structuring and supervising compliance for the study management plans
• Ensuring compliance with the project requirements and cascading the issues/ updates to the relevant stakeholders
• Supervising the site preparation, study implementation at site and ongoing study and QC activities to ensure good quality of study data
• Reviewing protocol deviations and loss to follow up to ensure quality data is delivered
• Communicating with investigators at THSTI and site investigator for tracking patient recruitment and progress to study timelines; maintaining and reporting metrics for clinical site performance
• Providing input and support to maintain appropriate documentation for adverse event safety monitoring, and collaborating in submission of safety reports to sponsor, Ethics Committees and other applicable authorities
• Willing to undergo training, conduct training and monitor study team performing of Neuro developmental assessment of infants • Liasoning with all stakeholders and IECs of all sites
• Providing support to site team to prepare for clinical audits and to respond to audit findings conducted by internal QA and external agencies.
• Supervising the data management progress with data manager and the DM team
• Work with coordinating PI to ensure that the trial is meeting its targets, is producing meaningful output and to predict and plan, any changes that warrant requests to changes in protocol, funding, or timelines
• Keeping stakeholders informed on study progress, risks and accomplishments, share reports, etc.
• Knowledge of adverse medical event investigation, analysis, and reporting procedures and standards
• Any other work as assigned by PI.
• The selected candidate may be posted at any of the following sites: AIIMS Delhi, VMMC & Safdarjung Hospital Delhi, ESIC Medical College Faridabad, or THSTI Faridabad, with occasional visits to the other sites as required.
Date of walk-in interview : 7th May 2026
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.
b) All educational, professional and technical qualifications should be from a recognized Board/University.
c) 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.
d) The date of Interview of the respective post will be the CRUCIAL DATE for determining eligibility with regard to age, experience, essential qualification etc.
e) 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 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.
f) All results/notifications will only be published on our website. Therefore, the candidates should essentially visit THSTI website, regularly.
g) All communications will only be made through email.
h) 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.
i) The no. of vacancy indicated above may change subjected to the actual requirement at the time of Written test/skill test/interview.
j) With regard to any provisions not covered in this notification, the bye laws of THSTI / Govt. of India rules / guidelines shall prevail.
k) Canvassing wrong information in any form will be a disqualification.
For posts mentioned above, interested candidates fulfilling the criteria as mentioned above may walk-in for written test/skill test/interview at 9:00 am on the date mentioned against each positions at THSTI, NCR Biotech Science Cluster, 3rd Milestone, Faridabad-Gurugram Expressway, Faridabad – 121001.
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.
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