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ICMR Delhi Life Sciences & Biotechnology Consultant Job Openings

ICMR Delhi Life Sciences & Biotechnology Consultant Job Openings. MSc Jobs. PhD Jobs. Life Sciences and Biotechnology Jobs. Consultant (Clinical Research Coordinator & Associate) Vacancies. ICMR Delhi Jobs. ICMR Delhi Careers. Interested and eligible applicants can check out all of the details on the same below

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INDIAN COUNCIL OF MEDICAL RESEARCH

Advt. No.: ITRC/ECD/1/2022

ICMR intends to engage following Non-Institutional project human resource positions, purely on a temporary contract basis for its short-term research projects, being undertaken at the Division of Epidemiology and Communicable Diseases (ECD) (Unit-Tuberculosis, Leprosy and Tribal Health), ICMR Hqrs, New Delhi.

Required qualifications and other details are given below.

Post I

Name of the Post – Consultant (Clinical Research Associate)

No. of Posts – 03

Place of Work – ICMR Hqrs., New Delhi

Max Age Limit – Upper age limit for up to 45 years. Age relaxation will be as per the Government of India/ICMR rules

Post II

Name of the Post – Consultant (Clinical Research Associate)

No. of Posts – 03

Place of Work – ICMR Hqrs., New Delhi

Max Age Limit – Upper age limit for up

to 45 years. Age relaxation will be as per the Government of India/ICMR rules

Post III

Name of the Post – Consultant (Clinical Research Coordinator)

No. of Posts – 03

Place of Work – ICMR Hqrs., New Delhi

Max Age Limit – Upper age limit for up to 45 years. Age relaxation will be as per the Government of India/ICMR rules

How to Apply

A walk-in-interview is scheduled for 22nd June 2022, 10:30 A.M. onwards for the following posts for which the details are given below. Interested and eligible candidates for the positions mentioned below may come for the walk-in interview and bring their CV in the prescribed format along with all relevant documents and one passport size photograph and any identity card from 22nd June 2022, 8.30 am onwards till 10:30 AM.

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 22nd June 2022 will not be entertained.

All the candidates who wish to appear for the interview should report at Reception, ICMR HQ, V Ramalinga swami Bhawan, Ansari Nagar, New Delhi on 22nd June 2022 at 8.30 AM till 10:30 AM for registration in room No. 322, 2nd floor, 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.

General Terms & Conditions

  1. A 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 Government hospital with not less than 40% disability.
  8. Separate applications 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 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. The persons engaged in Project Human Resource Positions cannot be permitted to register for PhD, due to time constraints.
  16. The persons engaged in Project Human Resource Positions 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. The 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 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 positions.
  18. Successful candidates will normally be engaged in Project Human Resource Position initially for a period of one year or less, depending upon the 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 duly filled in the application form in the prescribed format 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 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 Competent Authority 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 our website:https://main.icmr.nic.in/, regularly for further updates related to this advertisement.

For Post I

Essential Qualifications

  • 1st Class Master Degree in Life sciences/Biotechnology/Bio-Medical Sciences/M.Pharm or any equivalent degree from a recognized university with 4 years of experience or BAMS/BHMS/BDS/BV.Sc or any equivalent degree from a recognized university with 5 years of experience in Biotech/clinical research related to the development of clinical research.
    OR
  • 2nd Class Master’s Degree in Life sciences/Biotechnology or any equivalent degree + PhD degree in relevant subjects from a recognized university with 4 years of experience
    related to clinical research.

Desirable Qualifications

  1. PhD with 2 years post-Doctoral experience in biomedical subjects particularly in health research related areas. Working experience in Quality Control/Assurance.
  2. Knowledge of computer applications or business intelligence tools/data management/ data synthesis/Report writing, data mining, and working on databases.
  3. Thorough knowledge of GCP, and ICH guidelines and regulatory requirements for clinical trial conduct.

Job Requirement

The activities of the Consultant would include but are not limited to –

  • To follow SOPs for a clinical trial.
  • To monitor all aspects of study execution including assessing the site, capacity building, processes development of various steps of the clinical trial; follow study timelines and metrics.
  • The job requires frequent India travel to sites for monitoring and site audit
  • To participate in Site monitoring visits and oversee clinical monitoring activities ensuring compliance with Good Clinical Practices.
  • To prepare and/or review study-related Standard Operating procedures and Documents.
  • To develop and manage study master files and site files.
  • The job may require travel to the trial sites and attending outstation meetings. Any other job assigned by the competent authority.

Consolidated Emoluments – Rs. 60,000/- Fixed Per month

For Post II

Essential Qualifications

  • 1st Class Master Degree in Life sciences/Biotechnology/Bio-Medical Sciences/M.Pharm or any equivalent degree from a recognized university with 4 years of experience or BAMS/BHMS/BDS/BV.Sc or any equivalent degree from a recognized university with 5 years of experience in Biotech/clinical research related to the development of clinical research. OR
  • 2nd Class Master’s Degree in Life sciences/Biotechnology or any equivalent degree + PhD degree in relevant subjects from a recognized university with 4 years of experience
    related to clinical research.

Desirable Qualifications

  1. PhD with 2 years post-Doctoral experience in biomedical subjects particularly in health research related areas. Working experience in Quality Control/Assurance.
  2. Knowledge of computer applications or business intelligence tools/data management/ data synthesis/ Report writing, data mining, and working on databases.
  3. Thorough knowledge of GCP, and ICH guidelines and regulatory requirements for clinical trial conduct

Job Requirement

The activities of the Consultant would include but are not limited to –

  • To follow SOPs for a clinical trial.
  • To monitor all aspects of study execution including assessing the site, capacity building, processes development of various steps of the clinical trial; follow study timelines and metrics.
  • The job requires frequent India travel to sites for monitoring and site audit
  • To participate in Site monitoring visits and oversee clinical monitoring activities ensuring compliance with Good Clinical Practices.
  • To prepare and/or review study-related Standard Operating procedures and Documents.
  • To develop and manage study master files and site files.
  • The job may require travel to the trial sites and attending outstation meetings. Any other job assigned by the competent authority.

Consolidated Emoluments – Rs. 31,000/- Fixed Per month

For Post II

Essential Qualifications

  • Professional having M.Sc in Biomedical sciences or B.Tech (Comp. Science, Biotechnology or B Pharm or any equivalent degree from a recognized university with 2
    years’ experience in biomedical research particularly in clinical studies/trials.

Desirable Qualifications

  1. Post graduate degree in relevant subjects
  2. Knowledge of computer applications or business intelligence tools/data management/ data synthesis/Report writing, data mining, and working on databases.

Job Requirement

The activities of the Consultant would include but are not limited to –

  • To follow SOPs for a clinical trial.
  • To monitor all aspects of study execution including assessing the site, capacity building, processes development of various steps of the clinical trial; follow study timelines and metrics.
  • The job requires frequent India travel to sites for monitoring and site audit
  • To participate in Site monitoring visits and oversee clinical monitoring activities ensuring compliance with Good Clinical Practices.
  • To prepare and/or review study-related Standard Operating procedures and Documents.
  • To develop and manage study master files and site files.
  • The job may require travel to the trial sites and attending outstation meetings. Any other job assigned by the competent authority.

Consolidated Emoluments – Rs. 31,000/- Fixed Per month

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