BRIC-THSTI Job Openings – Clinical Research & Quality Roles, Apply Now!
RECRUITMENT NOTICE NO.: THS/RN/07/2025
BRIC-THSTI, an autonomous institute under the Department of Biotechnology, Govt. of India, is hiring for multiple positions in clinical research and quality management. If you’re a life sciences professional seeking impactful roles in regulatory and translational health research, this is your opportunity to contribute to pioneering projects on maternal, fetal, and newborn health.
About BRIC-THSTI
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 is an integral part of the interdisciplinary NCR Biotech Science Cluster located at Faridabad, with the mission to conduct innovative translational research and to develop research collaborations across disciplines and professions to translate concepts into products to improve human health.
Recruitment Notification
BRIC-THSTI has built several inter-institutional collaborations and connectivity with industry, supported by well-trained research and laboratory teams. We are currently recruiting for the following positions:
- Project Title: “Effects of extreme heat on maternal, placental and fetal physiology, lactation and newborn health in India.”
- PI : Dr. Shinjini Bhatnagar/ Dr. Nitya Wadhwa
BRIC-THSTI Job Openings:
- Clinical Research Associate (Quality)
- Number of Posts: Two
- Monthly Consolidated Emoluments: Rs. 66,000/-
- Age Limit: 35 years
- Qualifications & Experience:
- Graduation degree in Life Sciences/ Pharmacy/ Public Health from a recognized university with three (3) years of post-qualification experience in clinical trial monitoring or as a clinical site coordinator.
- Master’s degree in Life Sciences/ pharmacy/ Public Health or other related discipline from a recognized university with at least one (1) year of post-qualification experience in clinical trial monitoring or as a clinical site coordinator.
- MBBS/ BDS/ BHMS/ BAMS/ BPT with atleast one (1) year of postqualification experience in clinical trial monitoring or as a clinical site coordinator.
- Skills required:
- Basic knowledge and ability to apply GCP and applicable regulatory guidelines.
- Computer skills, including proficiency in Microsoft Office applications.
- Strong written and verbal communication skills, including a good command of English, are required.
- Excellent organizational and problem-solving skills.
- Practical time management skills and the ability to manage competing priorities.
- Job description:
- Evaluate the quality and integrity of trial site practices related to the proper conduct of the protocol and adherence to applicable regulations.
- Escalates quality issues to the Quality Manager, Project Manager, and/ or senior management.
- Work with the Clinical Portfolio Management department as directed and with other internal departments on their requirements as and when required.
- The selected candidates will be posted at our clinical sites situated at Puducherry and Bilaspur.
2. Quality Manager
- Number of Posts: One
- Monthly Consolidated Emoluments: Rs. 87,000/-
- Age Limit: 45 years
- Qualifications & Experience:
- Post-Graduation degree in Life Sciences/ Biomedical Sciences/ Pharmacy/ Public Health, from a recognized university with four (4) years of demonstrated experience in clinical trial monitoring or clinical site management experience.
- The candidate must possess a valid GCP certificate.
- Desirable – Two (2) years of work experience in Quality Control and Quality Assurance in clinical research.
- Skills Required:
- Good understanding of needs for projects and job responsibilities.
- Extensive knowledge of GCP/GLP, observational studies, and appropriate regulations and guidelines.
- Ability to develop and implement clinical and laboratory monitoring plans, SOPs, database concepts, and formats.
- Ability to build effective project teams, motivate others, delegate, drive, and make
timely/ quality decisions. - Operational skills, including focus and commitment to quality management and problem solving.
- Influencing skills, including negotiation and teamwork.
- Practical communication skills are needed to provide timely and accurate information to all stakeholders.
- Ability to assess noncompliance situations, recognize the potential or actual broader strategic risk to the project, and escalate when needed.
- Ability to identify systematic causes of complex quality problems and recommend long-term solutions.
- Create a fair and ethical culture that fosters high standards of ethics.
- Basic business computer skills (MS Word, Excel, e-mail)
- Job description:
- Setting up the trial sites such that each centre has the trial materials, including the trial supplies, while ensuring all trial supplies are accounted for in the study.
- Administers protocol and related trial training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
- Conduct source document verification and case record forms for assessing the study trends.
- Management of essential documents for the duration of the trial at CDSA.
- Develop a quality monitoring plan, SOPs, checklists, and processes for clinical activities of data collection, laboratory-based activities of sample processing and storage, and running of the biorepository.
- Collaborate with clinical and project management teams to ensure compliance with quality standards, timelines, and appropriate follow-up in areas of deficiency.
- Coordinate expert monitoring visits/ audits as per project requirements.
- Work with the Clinical Portfolio Management department and other internal departments on their requirements as and when required.
- Work with data management and other key departments (laboratory, etc.) to track the process and progress and proactively ascertain the foreseen challenges.
- The selected candidates will work at our clinical site situated at the Gurugram Civil Hospital.
3. Project Technical Support-III
- Number of Posts: One
- Monthly Consolidated Emoluments: Rs. 28,000/- plus HRA
- Age Limit: 35 years
- Qualifications & Experience:
- Graduation degree in any branch of Life Sciences from a recognized university with three (3) years of post-qualification experience.
- Post-Graduation degree in any branch of Life Sciences from a recognized university.
- Skills required:
- Experience in cell line culture and maintenance
- Experience in working with mouse models
- Experience with Molecular Techniques like RNA isolation, RT-PCR, Western Blotting, ELISA, etc.
- Proficient in working with computational software, including Microsoft Excel, PowerPoint, etc.
- Good communication and writing skills.
- Job Description:
- In-vitro and in-vivo modelling of lung fibrosis
- Blood collection from a mouse and performing biochemical investigations like ELISA, etc.
- Western blotting and other molecular techniques, including RT-PCR, transfection studies, gene overexpression, or knockdown studies in human cell lines
- Maintenance and culture of human cell lines
- Sample preparation for Proteomics studies and related data analysis
- Data compilation, presentation, and report writing.
Last date for receipt of online application: 19th May 2025
The applications will be scrutinised/shortlisted, and processed for further selection.
Keywords: BRIC-THSTI Job Openings, Recruitment, Job Posting, Clinical Research, Quality Manager, Project Technical Support, Life Sciences, GCP, Monitoring, Regulatory Guidelines, Clinical Trials
