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-I (Senior Clinical Research Associate) (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. 56,000/- plus HRA
Age Limit : 50 years
Date of walk-in interview : 16th June 2026
Essential & Desirable qualifications & Experience : Post Graduate Degree, including the integrated PG degree, in Life Sciences/ Pharmacy/ Public Health or any related discipline from a recognized university.
Desirable : • Possession of a valid Good Clinical Practice (GCP) certificate.
• Minimum two (2) years of experience as a Clinical Research Associate, Clinical Research Coordinator, or Site Manager in academic or phase clinical trials.
Skills required :
• Ability to work independently with minimal guidance and collaboratively in a team setting.
• Leadership skills, including building effective project teams, motivating others, delegating, and making timely/quality decisions.
• Business/operational skills with commitment to quality management and problem- solving.
• Effective communication ensuring timely and accurate stakeholder information; proficient in English with strong written and oral skills. Proficient in Excel, Word, PowerPoint, and Access.
• Strong writing skills for presentations, technical reports, manuscripts, monitoring plans, and SOPs.
• Understanding of Indian Clinical Trials Regulations, ICH, and CDSCO GCP; knowledge of human subject research regulations.
• Personal qualities: trust- building, learning ability, managerial courage, prioritisation, action-oriented, and adaptability.
• Influencing skills, including negotiation and teamwork.
Job description/ Skills required :
• The candidate will be responsible for overall monitoring, quality oversight, management, and operational execution of assigned clinical studies and sites under the supervision of the Chief CPM/ designee.
• Ensure trial integrity through onsite and central/remote monitoring, including review of data, processes, essential documents, and site performance metrics.
• Conduct site qualification, initiation, routine monitoring, and close-out visits for assigned trials, with willingness to travel across India at short notice and stay for extended periods as required.
• Perform central monitoring through regular review of trial data, deviations, trends, protocol compliance, and risk indicators to identify site issues early.
• Maintain, review, and ensure completeness of TMF and site ISF in compliance with GCP and regulatory requirements.
• Establish and maintain effective communication with sites for follow-up on study progress, documentation, data entry, query resolution, and compliance.
• Track site performance metrics, including recruitment, data quality, protocol adherence, timelines, responsiveness; provide feedback and corrective guidance as needed.
• Ensure high-quality delivery of tasks with strict adherence to project timelines, milestones, and deliverables.
• Understand and apply requirements of regulatory and funding bodies such as DBT, ICMR, HMSC, and others, ensuring compliance.
• Establish quality assurance procedures and predefined quality checkpoints across the project lifecycle.
• Prepare study-specific risk assessment and mitigation plans and ensure implementation through onsite and central monitoring.
• Develop and implement procedures ensuring adherence to protocols, GCP, SOPs, and administrative requirements.
• Develop and deliver project-, protocol-, and GCP-related training to site staff and project team members as required.
• Continuously monitor trial progress for compliance, identify operational challenges, and implement timely CAPA.
• Work with Investigators to meet recruitment targets, ensure outputs, and anticipate protocol amendments, funding revisions, or timeline changes.
• Lead development, review, approval, and distribution of study documents, including CRFs, protocols, manuals, monitoring tools, and other materials.
• Coordinate with data management and other teams to track study progress, milestones, data quality, and operational challenges.
• Communicate with internal teams regarding scope, timelines, goals, technical updates, and operational issues.
• Provide operational guidance, training, task allocation, and performance evaluation for study monitors and project team members.
• Undertake any other assignments from the Clinical Portfolio Management team as per project or organisational requirements.
Lab Technician (One post)
Project : Multiplexed Rapid Antigen test for dominant arbovirus (Dengue, Zika and Chikungunya Virus
PI : Dr. Gaurav Batra
Monthly consolidated emoluments : Rs. 20,000/- plus HRA
Age Limit : 50 years
Date of walk-in interview : 11th June 2026
Essential & Desirable qualifications & Experience : B.Sc. in any branch of Life Sciences from a recognized university. OR Three-year Diploma in Engineering and Technology.
Job description/ Skills required : Experience in the preparation of culture media, buffers, agarose gel, PAGE, inventory management, bacterial work, mammalian work etc.
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.
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.
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