ICMR MSc Biotech & Life Sciences Project Scientist Job Opening

ICMR MSc Biotech & Life Sciences Project Scientist Job Opening

ICMR MSc Biotech & Life Sciences Project Scientist Job Opening. MSc Jobs. MSc Jobs. Biotechnology and Life Sciences job openings. ICMR Delhi Jobs. ICMR Delhi Careers. Interested and eligible applicants can check out all of the details on the same below

This job expires in

Indian Council of Medical Research
New Delhi-110029

Advt.No.:ITRC/ECD/3/2022

The following posts are to be filled purely on a contractual basis for working under its various projects in India TB Research Consortium (ITRC), under the Division of Epidemiology and Communicable Diseases (ECD) ICMR Hqrs, New Delhi, through walk-in Interviews on 16th November 2022 at 10.30 am onwards.

Required qualifications and other details are given below

Name of the Post – Project Scientist Support-V (Clinical Operations) (For ITRC)

No. of Posts – One (UR)

Max Age Limit – Upper age limit for up to 40 Years, Age relaxation will be as per the Government of India/ICMR rules.

How to Apply –

All the Deserving candidates who wish to appear for the interview should report on 16/11/2022 along with 5 copies of their Bio-data. The candidates must reach on 16/11/2022 from 8.30 AM till

10:30 AM for registration in ICMR-HQ. The verification of the documents of the candidate will start from 8:30 AM onwards and eligible candidates after verification would be interviewed from 10:30 AM onwards.

Candidates applying for more than one post should indicate the names of the post clearly on the application form.
Applicants coming after 11.00 AM on 16th November 2022 will not be entertained.

Terms and Conditions 

1. The number of positions may vary.
2. These positions are meant for temporary projects and co-terminus with the project.
3. Engagement in the above advertised Project Human Resource positions will depend upon the availability of funds, functional requirements and approval of the competent authority. Therefore, we are not committed to filling up all the advertised Project Human Resource positions and the process is liable to be withdrawn/cancelled/modified at any time.
4. The rates of emoluments/stipends shown in this advertisement are project-specific and may vary according to the sanction of the funding agency of the Project.
5. The cut-off date for the age limit will be the date of the last date for the submission of applications.
6. Age relaxation will be as per the guidelines of ICMR.
7. Reserved category candidates must produce their latest Caste Validity Certificate. OBC candidates must possess the latest valid non-creamy layer certificate. PWD candidates shall produce the latest disability certificate issued by a Medical Board of a Government hospital with not less than 40% disability.
8. A separate application should be submitted for each position. Allotment of the project to the successful candidates will be decided by the competent authority at its discretion.
9. Qualification & experience should be in a relevant discipline/field and from an Institution of repute. Experience should have been gained after acquiring the minimum essential qualification.
10. Mere fulfilling the essential qualification does not guarantee the selection.
11. Persons already in regular time-scale service under any Government Department / Organization are not eligible to apply.
12. No TA/DA will be paid to attend the interview / personal discussion and candidates have to arrange transport/accommodation themselves.
13. ICMR reserves the right to consider or reject any application/candidature.
14. Submission of wrong or false information during the process of selection shall disqualify the candidature at any stage.
15. Persons engaged in Project Human ResourcePositions cannot be permitted to register for PhD, due to time constraints.
16. Persons engaged in Project Human ResourcePositions will normally be posted at the study site; however. they can be posted to any other sites in the interest of research work. They are liable to serve in any part of the country.
17. Persons engaged in Project Human Resource Positions shall not have any claim on a regular post in ICMR or in any of its Institutes/Centers or in any Department of Government of India and their project term with breaks or without breaks in any or multiple projects will not confer any right for further assignment or transfer to any other project or appointment/absorption/regularization of service in funding agency or in ICMR. Benefits of the Provident Fund, Pension Scheme, Leave Travel Concession, Medical claim, Staff Quarters and other facilities applicable to the regular staff of ICMR etc. are not admissible to the project human resource.
18. Successful candidates will normally be engaged in Project Human Resource Position initially for a period of one year or less, depending upon the sanctioned tenure of the Project and functional requirements. Continuation / Extension to the engagement of Project Human Resource Positions will be depending upon evaluation of performance, tenure of the project, availability of funds, functional requirements and approval of Competent Authority. The maximum term of any Project Human Resource Position in any or multiple projects, with breaks or without breaks shall be five years only. The concerned Project Investigator, Division Head and Head of the host Institute shall personally be responsible and accountable for the continuation/extension given if any without prior concurrence of the Director-General, ICMR to any project human resource position beyond five years either with or without breaks in any or multiple projects.
19. ICMR reserves the right to terminate the project human resource position even during the agreed contract
    period or extended contract period without assigning any reason.
20. Leave shall be as per the ICMR’s policy for project human resource positions.
21. Candidate must submit his/her online application form in https://projectjobs.icmr.org.in portal with a recent passport-size colour photograph along with a detailed bio-data/C.V. and all relevant documents; duly self-attested; in proof of his/her educational qualifications [all certificates and mark-sheets from 10th Std. onwards], working experience, age, caste and photo id [Aadhar Card/Indian Passport/PAN Card/Driving License] etc., within the scheduled date and time for submission of the application, failing which his/her candidature will not be considered. Late/Delayed/Incomplete/Unsigned applications will not be considered at all and no correspondence will be entertained in this regard.
22. ICMR reserves the right to cancel/modify the process at any time, at its discretion.
23. The decision of the DG, and ICMR will be final and binding.
24. Canvassing in any form will be a disqualification.
25. Corrigendum/addendum/further information; if any; in respect of this advertisement, will be published on our website only. Hence, the candidates are advised to see the website ICMR regularly for further updates related to this advertisement.

Essential Qualifications –

• 1st Class Master Degree in Biotechnology/Clinical Pharmacology/ M. Pharm/life sciences or any equivalent degree from a recognized university with 4 years experience in CRO industry /Pharma/Biotech/ Public Health/clinical research.
  OR
• 2nd Class M. Sc. / M. Pharm or any equivalent degree + PhD degree in Biotechnology/ Pharmacology/ M.Pharm Life sciences from a recognized university with 2 years of experience in Pharma /Biotech/CRO industry/ Public Health/ Clinical research.

Desirable Qualification :

1. PhD with at least 2 years post-Doc experience in biomedical subjects, particularly in health research-related areas. Working experience in scholarly publications.
2. Knowledge of computer applications or business intelligence tools/data management/data synthesis/Report writing, data mining, writing articles/ working on databases.
3. Knowledge of New Drug and Clinical Trial Rules 2019 (Schedule Y), GCP, ICH guidelines and regulatory requirements for clinical trial conduct.

Nature of duties

1. Protocol writing, Monitoring the clinical trial including safety data and ensuring timely completion of targets.
2. Source data verification, Monitoring vaccine trial, monitoring e CRFs data entry and query resolution.
3. Review and submit SAE and update the SAE document repository.
4. Prepare patient tracker to ensure compliance and minimize missing visits
5. Monitor site performance for project targets, and project staff for patient compliance.
6. Monitor the conduct of processes contributing to the performance of a clinical trial.
7. Prepare annual reports of projects and quality trending reports.
8. Prepare weekly site wisely and consolidated site report regarding enrollment /FU data for targets vs achievement.
9. Keep up to date with all quality and compliance issues for quality levels of the staff, systems and production activities.
10. Any other job assigned by the PI or Programme officer. The job requires frequent All India travel to sites for monitoring, quality assurance and quality management for at least 15 days a month.

Consolidated Emoluments per month – Rs. 57,660/- Fixed per month

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