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 Research Scientist-II (One post)
Project : Placenta Health Project - Adaptive Dose Finding Platform in India
PI : Dr. Nitya Wadhwa
Co-PI : Dr. Dinesh Mahajan
Monthly consolidated emoluments : Rs. 67,000/- plus HRA
Age Limit : 40 years
Essential & Desirable qualifications & Experience : Post Graduate Degree, including the integrated PG degree, in Life Sciences from a recognized university with at least three (3) years’ of post-qualification experience in a research lab.
OR Ph.D. in Life Sciences from a recognized university.
Desirable :
• Knowledge of establishing, maintaining, and characterizing placental organoid cultures for disease modelling and therapeutic research.
• Strong understanding of molecular and cellular biology techniques.
Job description/ Skills required : • Developing and optimizing Lateral Flow Assays (LFA) for diagnostic and analytical applications. • Maintaining accurate experimental records and preparing technical reports and presentations.
• Collaborating with multidisciplinary teams to support ongoing research and development projects.
• Ensuring compliance with laboratory safety standards and quality control procedures.
Date of walk-in interview : 19th June 2026
Research Scientist (Senior Bioanalyst) (One post)
Project : Placenta Health Project - Adaptive Dose Finding Platform in India
PI : Dr. Nitya Wadhwa
Co-PI : Dr. Dinesh Mahajan
Monthly consolidated emoluments : Rs. 1,20,000
Age Limit : 45 years
Essential & Desirable qualifications & Experience : Master’s degree in chemistry / Analytical Chemistry/ Pharmaceutical Sciences/ Pharmacology or a related discipline from a recognized university with atleast four (4) years’ of post-qualification experience in the following areas-
a) Hands-on experience in LC- MS/ MS-based bioanalysis, preferably in BA/BE setups, CRO, or translational research laboratories.
b) Experience in bioanalytical method development, validation, and analysis of PK samples in a regulatory- compliant laboratory.
Desirable : • Experience in establishing or setting up a bioanalytical laboratory or implementing compliant analytical workflows. Familiarity with bioanalytical regulatory guidance (e.g., USFDA and EMA) and laboratory quality systems is essential. Knowledge of ICH M10 bioanalytical method validation guidance and awareness of 21 CFR Part 58 (GLP regulations) will be an advantage.
Job description/ Skills required : • Laboratory Operations & Instrumentation
• Contribute to the establishment and operationalisation of the bioanalytical laboratory, including development of analytical workflows, laboratory processes, and documentation systems.
• Preparation and implementation of SOPs, laboratory practices, and quality-compliant procedures.
• Operate, troubleshoot, and maintain LC-MS/MS and HPLC systems to ensure reliable analytical performance.
• Support instrument qualification, calibration, preventive maintenance, and performance verification of laboratory equipment.
• Maintain accurate laboratory records and ensure adherence to laboratory safety and good documentation practices.
• Provide routine supervision and technical guidance to junior analysts and laboratory staff.
• Oversee the maintenance of reference standards, reagent inventory, logbooks and lab notebooks. Quality & Regulatory Compliance • Contribute to the revision of Standard Operating Procedures (SOPs), analytical workflows, and controlled documentation. • Support implementation of GCP- aligned and quality-compliant bioanalytical processes for regulatory clinical studies.
• Participate in internal audits, instrument qualification activities, and inspection readiness initiatives. Bioanalytical Method Development & Validation
• Prepare method development, validation, and analytical protocols for new projects after required literature search.
• Develop, optimize, and validate LC-MS/MS and HPLC methods for quantification of small molecule-based drugs and metabolites in biological matrices (e.g., plasma, serum, tissues).
• Execute regulatory bioanalytical validations aligned with national and international guidance (e.g., USFDA/EMA/ICH).
• Perform routine bioanalysis of clinical and preclinical PK study samples, including preparation of calibration standards and quality control samples.
• Generate analytical summaries, concentration datasets, and bioanalytical study reports in compliance with laboratory quality systems.
Date of walk-in interview : 29th June 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 a basicdegree as MBBS/ BDS from arecognized university, includingthe 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 as verbal communication skills.
• Computer skills, including proficiency in use of Microsoft Office applications.
• Good organisational 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 : 25th June 2026
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.
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.
a) All results/notifications will only be published on our website. Therefore, the candidates should essentially visit THSTI website, regularly.
b) All communications will only be made through email.
c) 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.
d) The no. of vacancy indicated above may change subjected to the actual requirement at the time of Written test/skill test/interview.
e) With regard to any provisions not covered in this notification, the bye laws of THSTI / Govt. of India rules / guidelines shall prevail.
f) Canvassing wrong information in any form will be a disqualification.
See All B.Pharm Alerts M.Pharm Alerts M.Sc Alerts Delhi Alerts
See All Other Jobs in our Database
Subscribe to Pharmatutor Job Alerts by Email
