Sunday, October 11, 2026
Project Associate at SIR-CENTRE FOR CELLULAR AND MOLECULAR BIOLOGY Hyderabd
Wednesday, October 7, 2026
Project Research Scientist at SJRI Bangalore
Tuesday, October 6, 2026
Project Research Scientist-I at Rajiv Gandhi Centre for Biotechnology (BRIC-RGCB), Thiruvananthapuram, Kerala.
Adv. 10/2026 | 01.10.2026
Applications are invited from suitable candidates (Indian Citizens) for one position of Project Research Scientist-I (Non-Medical) in the ICMR/MAHA MedTech -funded project titled "An AI-Integrated Ultrasensitive Nanopore Sensing System for Non-invasive Early Detection of Cervical Cancer" to work in the Laboratory of Dr. Mahendran K R, Scientist E-II at Rajiv Gandhi Centre for Biotechnology (BRIC-RGCB), Thiruvananthapuram, Kerala.
Essential Qualifications
- MSc or equivalent degree in any branch of Life Sciences, with 70% marks.
- Minimum of one year of experience in Membrane Protein Purification. A documented experience certificate is required.
Desirable Qualifications
- Minimum of one year of experience in handling Biophysical techniques.
Age
Below 35 years on 14th October 2026. Age relaxation will be given as per Govt. of India norms.
Emolument
₹ 56,000/- + 20% HRA per month
Duration
Initially for a period of one year or till termination of the project whichever is earlier and extendable based on the performance evaluation.
Selection Process
- Applications should be submitted online.
- Candidates currently working in Government firms should send applications through proper channel.
- Last date for receiving completed applications is 14th October 2026.
- If a candidate wishes to apply for different positions, separate application forms should be submitted for each position.
- Selection to the position will not entitle the candidate to any future positions at RGCB (permanent or otherwise). As with all project positions at RGCB, the position will be co terminus with end of the project.
Applications which are not in the prescribed format will summarily be rejected.
Only those fulfilling the above criteria need apply. Applicants will be short listed for the online selection interview based on eligibility criteria. Selection of suitable candidates will be made based on qualifications and performance in the selection interview.
Monday, October 5, 2026
Project Technical Support at IIT Madras
Sunday, October 4, 2026
Technical Officer
Wednesday, September 30, 2026
Project Research Scientist at SJRI Bangalore
Project Research Scientist -I (Non Medical)- ICMR BLUE SHOCK Trail Project
Job Summary:
Septic shock is a common and highly lethal ICU condition; Indian ICU data report mortality of up to 50–55%. A key driver of refractory vasodilation is excessive nitric oxide production through the NO–cGMP pathway. Methylene blue, an inhibitor of this pathway, is inexpensive and widely available, but high-quality evidence on its early use in septic shock — particularly from Indian ICUs — is lacking.
BLUE-SHOCK is a single-centre, prospective, randomized, open-label, blinded outcome assessment (PROBE), parallel-group controlled trial. One hundred adults meeting Sepsis-3 criteria for septic shock will be randomized 1:1, within 24 hours of vasopressor initiation, to receive either adjunctive intravenous methylene blue along with standard guideline-based care, or standard care alone.
The primary outcome is time to shock reversal (cessation of vasopressors for ≥ 6 consecutive hours). Secondary outcomes include cumulative norepinephrine-equivalent dose, mean arterial pressure, cardiac output and systemic vascular resistance over the first 48 hours, lactate clearance, duration of mechanical ventilation, ICU length of stay, 28-day mortality, adverse events, and ICU treatment cost. The study will also explore biomarker-based (IL-6, procalcitonin) and hemodynamic phenotypes associated with treatment response.
Salary : Rs.72,800/- p.m
No of Vacancy : One
Key Responsibilities:
Overall day-to-day scientific and operational management of the trial, including:
- Screening of ICU admissions against Sepsis-3 eligibility criteria and maintenance of the screening and enrolment log.
- Coordinating the informed consent process with the investigators, including consent from legally authorized representatives and re-consent on recovery of capacity
- Implementing randomization and allocation concealment procedures (sequentially numbered opaque sealed envelopes) and safeguarding allocation records.
- Supervising administration of the study intervention per protocol and monitoring protocol adherence and deviations.
- Coordinating advanced hemodynamic monitoring (cardiac output, SVR, stroke volume variation), serial ABG/lactate sampling and biomarker (IL-6, procalcitonin) collection, storage and assay scheduling with the laboratory.
- Supervising the work of the Project Technical Support–III staff and ensuring complete, accurate and timely CRF completion.
- Database design and management, data quality control, periodic data audits, query resolution and preparation of the final cleaned dataset.
- Coordinating statistical analysis with the study statistician and assisting in interpretation of results.
- Recording, documenting and reporting adverse events and serious adverse events to the PI and the Institutional Ethics Committee; maintaining pharmacovigilance and safety records.
- Maintaining regulatory and ethics documentation, CTRI registration and updates, SOPs and the trial master file; preparing progress, utilization and interim reports for ICMR.
- Assisting in training of investigators and ICU staff on protocol and data collection procedures.
- Assisting in preparation of manuscripts, conference presentations and the final project report.
- Any other scientific or administrative task assigned by the Principal Investigator in connection with the project.
Eligibility Criteria:
Preferred Qualifications:
Essential:
- First Class post-graduate degree, including an integrated post-graduate degree, in Life Sciences / Biotechnology / Microbiology / Biochemistry / Pharmacology / Clinical Research / Public Health or an allied discipline from a recognized university; OR
- Second Class post-graduate degree, including an integrated post-graduate degree, with a Doctorate degree (Ph.D.) in a relevant subject from a recognized university.
Desirable:
- Ph.D. or M.Phil. in a relevant subject; or a post-graduate qualification in clinical research / clinical epidemiology.
- GCP (Good Clinical Practice) and ICMR National Ethical Guidelines certification.
- Working knowledge of biostatistics and statistical software (SPSS / R / STATA) and of electronic data capture systems (REDCap or equivalent).
- Prior publications in peer-reviewed journals
Age Limit: 35 Years
Preferred Language: English
Tentative Date of Joining : 15th October 2026
To Apply: E-mail cover letter and curriculum vitae with 3 references (names and email addresses / phone numbers) by on or before 9th October 2026 to mathangi.krishnakumar@stjohns.in & cc to hr@sjri.res.in