60 Principal Investigator Jobs - Page 2

Job Description: Applications are invited for the post of Project Research Scientist - I (Non-Medical) for the ICMR New Extramural (First in the World Challenge) grant in the Centre for Nanobiotechnology (CNBT), at Vellore Institute of Technology (VIT). (No. EM/Dev/FIW/00252/2024 (E-Office-227016)). Title of the Project: First in the World Challenge: A Nasal Spray Formula for Pulmonary Delivery to Control Multidrug-Resistant Tuberculosis MDR-TB Qualification: The candidate must have a first-class postgraduate degree, including the integrated PG degrees, relevant to nano technology, nano-delivery, biological therapeutics, pharmaceutical sciences, Biotechnology. Stipend: Rs. 56,000 + 10% HRA (Rs. 61,600) per month, stipend will be as per Institute norms. Sponsoring Agency: ICMR, New Delhi Duration: 3 years Principal Investigator: Dr. Natarajan Chandrasekaran, Professor, Higher Academic Grade, Centre for Nanobiotechnology (CNBT), Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu Co-Principal Investigator: Dr. George Priya Doss C, Professor Grade 1, Department of Integrative Biology School of Bio Sciences and Technology Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc on or before (10/06/2025) through online http://careers.vit.ac.in No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

Role & responsibilities 1. Act as a Principal Investigator / Co-investigator in phase-1 studies, Biosimilar and BA/BE studies in all therapeutic area as well as various kind of formulation. 2. Feasibility assessment of different molecules as per request from sponsors. 3. Conducted complex BA/BE study at hospital site as Principal Investigator. 4. Involved in Audit/Inspection handling and Projects conducted as Principal Investigator have been audited and cleared by different regulatory. 5. Leading and guiding the Research Staff as Team Lead. 6. Prepare and review protocols for clinical studies 7. Ensure compliance to protocol, SOPs and Regulatory requirements 8. Communicate IEC related issues to all concerned 9. Coordinate with Project Coordinators for all project related matters 10. Monitor and manage adverse events 11. Coordinate with panel of consultants to seek medical opinion as and when required 12. Ensure timely response to QA findings 13. Interact with sponsors on medical related matters 14. Handle safety related issues and ensure appropriate communication 15. Prepare and review reports for clinical studies 16. Overall supervision of screening and check-in activities 17. Write and review related SOPs 18. Contribute towards scientific development of the organization 19. Support clinical trial group 20. Handle medical confidential report and case management 21. Help maintain and update all the systems and SOPs in the department 22. Train the staff on CPR, GCP and related guidelines and all departmental and relevant SOPs. 23. Any other responsibilities as assigned by the Head of the Department

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS Department: Bioanalytical Operations Designation: Research Associate Job Location: Ahmedabad (Gujarat) Education: M.Pharm/B.Pharm Experience: 5 to 7 years CTC Range: 5 to 7 Lacs Job Description: Ensure project coordination and conduct the study as per protocol and SOPs requirements. Work in close coordination with the Principal Investigator and Study team. Review of study protocol, ICF, CRF and other appendices (applicable in case of Special studies). Handling study related IMPs and its relevant documents (IP retrieval, verification, accountability, dispensing etc.). Communicate with sponsors, other departments and team on appropriate aspects of the clinical studies. Compile and complete raw data in TMF and resolve all QA/QC queries in timely manner. COMPETENCIES Accountability Communication Work Ethic Presentation / Communication skills Organizational Culture fit

Project Research Scientist I (Non Medical)- ICMR PPBC Project Division Non Division User Contact Person Ms. Lincy Thomas Job Details Brief Description about the Project Postpartum Breast (PPBC) cancer is a unique subtype affecting young women who develop breast cancer within 5 to 10 years after the last childbirth. The project aims at investigating genomic, transcriptomic and spatial microenvironment and devise strategies for clinical decision to identify poor prognostic subclasses. Project Research Scientist I (Non Medical) No. of Vacancy: One Preferred Qualifications: MSc (first class) in Life sciences with 4 years of experience Maximum Age Limit : 35 years Salary: Rs.72800 /- per month Language : English Experience: Previous experience in cancer biology and big data analysis is preferred Last Day for Receiving Application: 19th July 2025 Location: Bangalore Roles and Responsibilities: To enable the collection of tumor tissue following the eligibility criteria, perform experiments for the genomic and spatial exploration, collation and analyses of the data, presentation of data, manuscript preparation, prepare the UC and reports to the granting agency. The Principal Investigator ICMR PPBC Project

Project Technical support - III- ICMR ICRAG-2 Project Division Non Division User Contact Person Ms. Lincy Thomas Job Details Brief Description about the Project A Multicentre multi-method study for development and Validation of a Deprescribing Tool, followed by Implementation and evaluation of its impact, facilitators and barriers. The study will be done in three main steps 1. Formative research using Systematic/Rapid Review, Mixed methods study and a qualitative study. The intervention components will be then prioritized using Delphi process and will be locally customised. 2. The IP will be evaluated through a cluster RCT for effectiveness, implementation research outcomes and cost effectiveness. 3. In this step, we will disseminate the findings and learnings of the study through symposia s and we will conduct effective policy dialogues with key stakeholders. Project Technical support - III No. of Vacancy: One Preferred Qualifications: 1. Three years Graduate in relevant subject / field + three years experience or PG in relevant subject / field 2. For Engineering / IT /CS first class four years Graduate Degree + Three years Experience Maximum Age Limit : 35 years Salary: Rs.36,400 /- per month Language : Good communication in English Experience: Two to three years experience in a recognized institute/hospital Knowledge of Computer Applications Experience in prescription data collection/analysis or research project Experience in Clinical data collection, including interviews/surveys Last Day for Receiving Application: 7th July 2025 Location: Bangalore Roles and Responsibilities: Overall coordinate the study; closely work with the Project Scientist and investigators. The Principal Investigator ICMR ICRAG-2 Project

1. Junior Research Fellow (JRF) (No. of Positions: 01) Project Technological advancement for the biomanufacturing of D-allulose, an ultra-low calorie functional sugar of anti-diabetic and anti-obesity potential Project investigator Prof. Sudhir Pratap Singh Qualifications: M. Sc. in any branch of life sciences from any reputed CSIR/UGC NET / GATE / or any other relevant/equivalent nature of test qualified. Responsibilities: Conduct high-quality research in molecular biology and industrial Design and execute experiments, analyze data, and interpret results. Collaborate with a multidisciplinary team of scientists and researchers. Present research findings and manuscript preparation. Assist in mentoring junior researchers and students. The selected JRF candidate may be allowed to enroll for PhD program as per Qualifications: Knowledge of molecular biology and enzyme kinetics technologies. Familiarity with bioinformatics tools and statistical software. Ability to work independently as well as part of a team. Excellent communication and interpersonal skills.

Project Technical Support-III (Audiology)-ICMR ENT CBR Project Division Non Division User Contact Person HR Job Details Brief Description about the Project ICMR funded project on Community based model for Early detection - Speech and language training of hearing impaired children - Mixed methods Implementation study Project Technical Support-III (Audiology) Position Starting: 1st July 2025 No. of Vacancy: one Preferred Qualifications: BASLP Maximum Age Limit : 35 years Salary: Rs 36,400/- Consolidated (Rupees thirty six thousand four hundred only including HRA) (This includes all expenses like statutory deductions etc.) Language : English , Kannada Experience: Fresher is acceptable Last Day for Receiving Application: 15th June 2025 Location: Bangalore Roles and Responsibilities : Perform and train anganwadi workers in screening Auditory Brain Stem Response, Data entry in excel The Principal Investigator

Screening in aspirational district Kadapa {recruitment of participants from Kadapa} and analysis will be carried out in St. John s Medical College Hospital. Screening for hemoglobinopathies in pregnant women and girls of childbearing age attending the OPD at Medical College hospital (RIMS, District Hospital), Kadapa Newborn screening for 5 parameters for all neonates born in District Hospital, Kadapa. Improve awareness about hemoglobinopathies & newborn screening. Phlebotomist (Field Worker) No. of Vacancy: Preferred Qualifications: BSc MLT / MSc MLT / BSc Nursing / PC BSc Nursing Language : Telugu, Hindi, Urdu, English, Tamil, Kannada Last Day for Receiving Application: 21st June, 2025 Roles and Responsibilities : For taking consent, administering the questionnaire, sample collection and sample transport The Principal Investigator DBT UMMID Project To Apply: E-mail cover letter and curriculum vitae on or before 21st June, 2025 to

Lab technician -DBT UMMID Project Division Non Division User Contact Person Ms. Lincy Thomas Job Details Brief Description about the Project Screening in aspirational district Kadapa {recruitment of participants from Kadapa} and analysis will be carried out in St. John s Medical College Hospital. Screening for hemoglobinopathies in pregnant women and girls of childbearing age attending the OPD at Medical College hospital (RIMS, District Hospital), Kadapa Newborn screening for 5 parameters for all neonates born in District Hospital Improve awareness about hemoglobinopathies & newborn screening. Lab technician Position Starting: 1st July 2025 No. of Vacancy: Two Preferred Qualifications: MSc Biochemistry / MSc Medical Biochemistry / MSc MLT Salary: Rs. 25000 per month (Consolidated) Language : English, Kannada Experience: 1-2 years Last Day for Receiving Application: 21st June, 2025 Location: Bengaluru, Karnataka Roles and Responsibilities : In SJMCH lab for sample processing, QC handling, data compilation The Principal Investigator DBT UMMID Project

Screening in aspirational district Kadapa {recruitment of participants from Kadapa} and analysis will be carried out in St. John s Medical College Hospital. Screening for hemoglobinopathies in pregnant women and girls of childbearing age attending the OPD at Medical College hospital (RIMS, District Hospital), Kadapa Newborn screening for 5 parameters for all neonates born in District Hospital Improve awareness about hemoglobinopathies & newborn screening. No. of Vacancy: One Preferred Qualifications: MSc Medical Biochemistry Language : English, Telugu, Kannada, Hindi, Urdu, Tami Last Day for Receiving Application: 21st June, 2025 Roles and Responsibilities : To coordinate between aspirational district and SJMCH lab for monitoring sample collection, processing, training, and awareness program implementation.

Implementation Research to develop an optimized model of comprehensive intervention package and delivery strategies to reduce stillbirth Assistant nursing superintendent No. of Vacancy: Preferred Qualifications: Master s degree in Community Nursing// Paediatric Nursing / Obstetric Nursing or Public Health or BSc nursing with experience in obstetrics and pediatric Last Day for Receiving Application: 18th June 2025 Roles and Responsibilities : Onsite mentoring and supportive supervision of nurse mentors and health care personnel in the health facilities within the district Training of nurse mentors & health care personnel in the health facilities Evaluation of competencies of health care personnel and ensuring the quality of data collected from health facilities. Capacity building and mentoring of research health personnel and project assistants. Report on the project activities being implemented to the core team at regular intervals. Plan and develop quality improvement initiatives at the health facilities to help achieve the project objectives

Strengthening Program Implementation and Monitoring to Achieve Single-digit Neonatal Mortality Data Entry Operator No. of Vacancy: Preferred Qualifications: Graduate or Intermediate or 12th pass in the science stream from a recognized board. Experience: Fresher or at least 1 year experience in Data Entry in research projects or any National Health program Last Day for Receiving Application: 18th June 2025 Roles and Responsibilities : Assist the central team in the data entry work related to the project. Data handling and entry of the captured data in the study portal. Implement data management procedures and ensure the accuracy and integrity of collected data. Utilize advanced data management tools and software to handle large datasets efficiently.

Preparation and Evaluation of Wound Dressing Material and Topical Ointment Using Magnetosome Conjugated Lemon Grass Extract (MLGE) Qualification: First Class Post-Graduate (PG) Degrees (M.Tech., M.Sc.,) degrees in Biotechnology /Botany /Microbiology or equivalent Describe if any Candidates having knowledge and hands-on experience in the area of animal work/herbal formulations / nanoformualtions / cell culture work will be preferred. Publication records relevant to the field. Fluent in English, both written and spoken.

Gujarat Biotechnology University is looking for Junior Research Fellow to join our dynamic team and embark on a rewarding career journey Research Support: JRFs work under the guidance of senior researchers or principal investigators on research projects They assist in conducting experiments, data collection, literature reviews, and data analysis Data Collection and Analysis: Collecting and recording data from experiments or research studies and using appropriate software or statistical tools for data analysis Literature Review: Conducting comprehensive literature reviews to understand the current state of research in the field and to inform the research design and methodology Experimental Work: Depending on the field, JRFs may perform laboratory experiments, fieldwork, surveys, or other research activities specific to their project Documentation: Keeping detailed records of research procedures, findings, and outcomes This documentation is critical for the research process and for publishing research results Research Proposal Writing: Assisting in the preparation of research proposals and grant applications to secure funding for research projects

Identify new sites, PIs and Assists in evaluating new protocols for feasibility at the site. To coordinate with Principal Investigator, Institutional Review Board/ Institutional Ethics Committee, Sponsor/CRO & Team for conduct of the clinical research/trials. Reviewing the protocol/synopsis and other materials, such as NDA, feasibility questionnaire and Approached to PIs as per study indication for further process discussion. Assessing the ability to meet the study timelines in light of other site commitments and overall feasibility Looking at subject eligibility requirements and determining if those subjects would be available in the practice. Assessing the resources necessary to do the study, including people, physical space, etc Collecting curriculum Vitae, MRC, and GCP Certificate of Principal Investigator, sub- Investigator and other study professionals, and send along with completed Site feasibility questionnaire. Assessing for Site Selection Visit (SSV) & Site Initiation Visit (SIV). To conduct the clinical trial according to ICH-GCP guidelines, New drugs and Clinical trials rules 2019, and other applicable regulatory guidelines. To systematize processes in order to attend high level of standards during research process. Preparing documents for submission to the Institutional Review Board (IRB)/ IEC Attending the Investigator meeting, as appropriate, and train staff about their duties related to the ongoing clinical trial. To obtain and document the Informed Consent form which should comply with the applicable regulatory requirements and adherence to GCP and to the ethical principles that have their origin in the declaration of Helsinki. Presenting the informed consent form to potential subject, discussing the consent and the study with them and answering questions. Obtaining subject s signatures on the informed consent forms, and ensuring that all necessary signature and dates are on the ICF. Documenting, distributing and filing assigned informed consent forms appropriately. Ensuring that all amended consent forms are appropriately implemented and signed. To ensure that neither the investigator nor the trial staff, should coerce or unduly influence a subject to participate or to continue participate in the trial. To ensure that the rights and we'll-being of the subjects are protected. To provide patient Information sheet to the subject. Contacting and screening potential subjects for the study. Recruiting Subjects, Scheduling Subject and Sponsor Visits. Preparing for each subject visit to ensure that all appropriate study procedures are done. Assisting the Investigator with study subject visits. Ensuring that All necessary data are gathered and recorded in the appropriate source documents (ie, Patient charts) and the case reports forms. Reviewing case report forms entries for completeness, correctness and logical sense in addition, review the source documents and case report orms for adverse events that may have been missed. Working with sponsor monitors (CRAs) during monitoring visits. Making corrections to the case report forms, if appropriate and resolving data queries. Managing laboratory procedures (drawing samples, Processing, packaging and shipping). Preparing Invoices and managing payments to study subjects, if appropriate. Preparing Invoices and managing payments to study subjects, if appropriate.

There is a high incidence of neurodevelopmental problems in neonates requiring NICU care. An early screening in the 1st 3 months of life is important to mitigate problems due to abnormal development. General Movements Assessment (GMA) is an easy, time-saving, non-intrusive, cheap method compared to MRI or other neurologic tests. It is also sensitive and specific. GMA can only be performed by certified and trained assessors which leads to limited availability and can restrict accessibility of this tool in remote areas. Thus, automating GMA would aid increased screening rates, scalability, standardisation, accuracy, and cost- effectiveness. The project involves acquiring high quality videos of high risk neonates, annotating them and developing an app that will automatically characterize them as normal or abnormal Project Technical Support-II No. of Vacancy: Preferred Qualifications: M.Sc/MA Psychology/Bachelor in Physiotherapy/Bachelor in Occupational Therapy Maximum Age Limit Salary: INR 26,000.00/- (Rs 20,000+30%HRA) English, Kannada, Tamil, Telegu Last Day for Receiving Application: 5th June, 2025 Roles and Responsibilities : Build rapport with parents by counselling, assistance to encourage follow-up

To help in studies of the Division, including development and evaluation of effectiveness of improved take home foods in combination with behaviour change intervention to improve nutritional status in children. We are seeking a Nutritionist to join our research team, to work both at SJRI and at our research field site (Shivamogga). No. of Vacancy: Preferred Qualifications: M.Sc. in Food Science and Nutrition/M.Sc. in Food Science and Technology Last Day for Receiving Application: 5th May, 2025 Location: St. John s Research Institute, Bengaluru and Shivamogga district (research field site) Roles and Responsibilities : The candidate will be responsible for overall activities of the research project at SJRI as well as at the field site in Shivamogga. Key duties include: Conduct and support all data collection activities, fieldwork, participant interviews, surveys, and nutritional assessments. Ensure accurate and timely data entry into the project database and assist in maintaining data integrity and confidentiality. Assist with monitoring the quality of data and identifying discrepancies or inconsistencies. Provide technical assistance in setting up and calibrating research instruments and tools Ensure compliance with Standard Operating Procedures (SOPs) for all project activities. Participate in regular field visits to monitor ongoing research activities and ensure adherence to research protocols. Contribute to the preparation of technical reports, presentations, and manuscripts for internal and external stakeholders. Assist in other studies and activities of the Division of Nutrition.

Title of the Project: First in the World Challenge: A Nasal Spray Formula for Pulmonary Delivery to Control Multidrug-Resistant Tuberculosis MDR-TB Qualification: The candidate must have first class in post graduate degree, including the integrated PG degrees, with three years post-qualification experience or PhD in Biotechnology experience in nanoemulsions preparation and drug delivery systems and antimicrobial studies.

: BE/B.Tech(CSE/IT/ECE/EEE) with Four years experience in Research and Development in Industry and Academic Institutions or Science and Technology Organizations and Scientific activities and Services OR Doctoral Degree in Engineering/Technology/MS from a recognized University/Equivalent Describe if any Candidates who have knowledge in programming, app development, image processing, full stack development, machine learning, deep learning and computer related field will be given preference Stipend : Rs. 42,000/- per month (as per eligibility) + HRA (as per norms) Sponsoring Agency : Ministry of Earth sciences, Government of India, New Delhi . Duration : 24 Months Principal Investigator : Dr. Swathi J N, Professor School of Computer Science and Engineering, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Co-Principal Investigator : Dr. Boominathan P, Professor School of Computer Science and Engineering, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Dr. Shashank Mouli Satapathy, Professor School of Computer Science and Engineering, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before ( 5/6/2025) through online http://careers.vit.ac.in No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

Consultant (Scientific Technical/Non-Medical) Qualitative -ICMR ICRAG-2 Project SJRI | St. Johns Research Institute Consultant (Scientific Technical/Non-Medical) Qualitative -ICMR ICRAG-2 Project Non Division User ICMR ICRAG 2 Project 080-49467010/49467011 Job Details Brief Description about the Project A qualitative study to explore health system barriers and facilitators for cardiovascular disease reduction. This project is part of a multicenter multi-method study (ICMR ICRAG 2 Project) for evaluating low-cost intervention package to reduce burden of cardiovascular diseases in India. Consultant (Scientific Technical/Non-Medical) Qualitative No. of Vacancy: Salary: Rs.50,000/- per month for 6 months can be extended up to 12 months. Experience: Candidate with work experience in at least two qualitative study projects and resultant published papers. Preferred Qualifications: MA/MSc/MSW/MPH/MHA/MD/PhD/Post Doc Last Day for Receiving Application: Roles Responsibilities: Translate and transcribe data onto Word/ NVivo Perform the first level (open) coding Involvement in data analysis, interpretation and manuscript write-up

Role & responsibilities: Ensures that qualified by education, training, and experience to assume responsibility for the proper conduct of the clinical studies. Maintaining current, up-to-date curriculum vitae . Assuming responsibility for the conduct of the clinical investigation. Signing the protocol Documenting the financial aspects of the trial. Disclosing conflicts of interest as described in the regulations. Ensuring adequate number of qualified staff and adequate facilities for conductance of the study properly and safely. Ensures that all persons assisting with the study are adequately informed about the protocol, the investigational product(s), and their study-related duties and functions. Ensuring that medical care is provided to a subject for any adverse event(s) that is reported. Informing a subject when medical care is needed to treat an inter-current illness. Provide information regarding adverse events and serious adverse events to the IRB/IEC. Possessing a thorough understanding of the requirements of each protocol . Ensuring recruitment goals are reasonable and attainable. Assessing overall protocol feasibility. Following the trials randomization procedures. Ensuring that the informed consent form contains the entire Essential and additional elements required. Conduct of the clinical studies specified by the applicable regulatory requirement(s), the IRB/IEC requirements and/or the regulatory authorities. Conduct the study as per the principles of ethics and is compliance with Good Clinical Practices (GCP). Attending education workshops. Reviewing professional publications. Participating in professional societies Maintaining a list of qualified persons and their corresponding trial-related delegated duties. Preferred candidate profile can send to email: hr@qpsbioserve.com or raghavendra.kundhula@qpsbioserve.com Perks and benefits: Nil

A Multicentre multi-method study for development and Validation of a Deprescribing Tool, followed by Implementation and evaluation of its impact, facilitators and barriers. The study will be done in three main steps 1. Formative research using Systematic/Rapid Review, Mixed methods study and a qualitative study. The intervention components will be then prioritized using Delphi process and will be locally customised. 2. The IP will be evaluated through a cluster RCT for effectiveness, implementation research outcomes and cost effectiveness. 3. In this step, we will disseminate the findings and learnings of the study through symposia s and we will conduct effective policy dialogues with key stakeholders. Consultant (Scientific Technical/Non-Medical) Qualitative No. of Vacancy: Salary: Rs.50,000/- per month for 6 months can be extended up to 12 months. Experience: Candidate with work experience in at least two qualitative study projects and resultant published papers. Preferred Qualifications: MA/MSc/MSW/MPH/MHA/MD/PhD/Post Doc Last Day for Receiving Application: Roles Responsibilities: Will be involved in the conduct of qualitative study for the 4-6 Intervention sites. This will involve in-depth interviews and focus group discussion among key stakeholders to identify barriers and facilitators at the site level for effective implementation of the intervention and willing to travel to other cities Interested candidates may send their Resume to:

To evaluate sensitivity and specificity of double fortified salt in real world conditions. No. of Vacancy: Salary: 20,000/- per month (including HRA) KANNADA must (optional: English, Hindi, Tamil, Telugu) Preferred Qualifications: 10 th PASS Last Day for Receiving Application: Roles Responsibilities: Test meal preparation for intervention studies. Clean and disinfect lab floors, surfaces, equipment, and work areas. Safely segregate and dispose of biological, chemical, and hazardous waste. Replenish lab supplies (e.g., gloves, soap, disinfectants) and assist with basic cleaning tasks. Report spills, damages, or hazards to the lab supervisor and maintain cleanliness logs if needed. Help in unpacking, labeling, and organizing lab materials and deliveries. Support in moving equipment, furniture, or supplies within the lab. Provide general support to lab staff during fieldwork or routine operations. Travel to field/home for data collection. Support any additional tasks assigned by the supervisor or Principal Investigator (PI) related to the project.

Vellore Institute of Technology is looking for JRF/ANRF-SERB/SCHEME/Dr K Sivagami to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes

It is a multicentre randomised controlled trial to study.The effects of steroids as against place to for the treatment of severe scrub pneumonitis. Preferred Qualifications: Bachelors / Undergraduate degree / Nursing / BSC / MSC Language : English should know , Preferable to know also -Kannada/ Tamil/ Telugu Should have name experience in research Roles and Responsibilities : Screening of study participants Recruiting patients for the study Help in taking informed consent for the study Ensuring in delivery of intervention drug/placebo Collect data for the study enter in the data base