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ICMR Delhi Jobs With Rs. 57,660 pm Pay For Biotech, Attend Walk-In

ICMR Delhi Jobs With Rs. 57,660 pm Pay For Biotech, Attend Walk-In. MSc Jobs. PhD Jobs. Non-Medical Biological Sciences Jobs. Project Scientist 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
Division of Epidemiology and Communicable Diseases, Unit-TB, Lep & TH

NOTIFICATION FOR WALK-IN-INTERVIEWS FOR THE VARIOUS PROJECT POSTS

Following posts are to be filled purely on a contractual basis for working under various TB projects under the Division of Epidemiology and Communicable Diseases (ECD) (Unit-Tuberculosis, Leprosy and Tribal Health), ICMR Hqrs, New Delhi.

Advertisement No. ITRC/ECD/1/2022

NOTE: All the posts are open to all caste categories

A. Project: Project Management Unit – India TB Research Consortium

Post I

Name of the Post – Project Scientist -V (Clinical Coordinator/QC)

No. of Posts – 01

Age – Upper age limit up to 40 years. (Relaxable to OBC and SC/ST Candidate as per
Govt. of India)

Tenure – Up to 31 March 2023, may continue for another year based on performance
evaluation report.

Place of Work

– ICMR Hqrs

Post II

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

No. of Posts – 01

Age – Upper age limit up to 40 years. (Relaxable to OBC and SC/ST Candidate as per
Govt. of India)

Tenure – Up to 31 March 2023, may continue for another year based on performance
evaluation report.

Place of Work – ICMR Hqrs

B. For Project Management Unit for ‘TB Vaccine trial’

Post III

Name of the Post – Project Scientist -V (Non-Medical) (Non-Medical)

No. of Posts – 01

Age – Upper age limit up to 40 years. (Relaxable to OBC and SC/ST Candidate as per
Govt. of India)

Tenure – Initially for one year. May continue till the duration of the project based on the performance evaluation report.

Place of Work – ICMR Hqrs

How to Apply

A walk-in-interview is scheduled for 22nd April 2022, 10:00 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 April 2022 from 9.00 am onwards till 11:00 AM only.

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 April 2022 will not be entertained.

All the candidates who wish to appear for the interview will be required to come in ai ICMR Hq,. V Ramalingaswami Bhawan, Ansari Nagar, New Delhi on 22nd April 2022 from 9.00 AM till 11:00 AM. And register in room No. 322, 2nd floor, ICMR HQ. The verification of the documents of the candidate will start from 9:00 AM onwards and eligible candidates after verification would be interviewed from 11:00 AM onwards.

Terms & Condition

  1. Departmental candidates or candidates working/have worked on projects of ICMR
    Institutes/ Centre shall be given age relaxation to a minimum of five (5) years or a
    completed months/year based on earlier project service, whichever is less, they meet the essential qualification and experience prescribed for the post, with a view to providing them with the opportunity to compare with other candidates.
  2. Age relaxation against posts earmarked for reserved candidates will be as per Govt. of India Norms and no age relaxation will be allowed in unreserved posts.
  3. Qualification and experience should be in a relevant discipline/field and from a reputed
    institution/organization recognized by the relevant authority. Experience shall count from the date of completion of minimum educational qualification.
  4. Submission of incorrect or false information during the process of personal discussion and/ shall disqualify the candidature at any stage.
  5. Mere fulfilling the essential qualification/experience does not guarantee selection.
  6. Candidates employed in Govt. Service/Semi Govt. Autonomous Bodies of State/Central
    Govt. should submit a “No Objection Certificate” from their employer.
  7. The above post is contractual for the duration offered may or may not be renewed subject to satisfactory performance and requirement.
  8. Age will be reckoned from the last date of receipt of application.
  9. These posts are purely temporary and co-terminable with the project. Employees will be
    on a consolidated pay basis.
  10. The appointment will be made on the basis of the results of a personal discussion/ interview.
  11. The selected candidate will not have any right to claim for a regular appointment in the council on the basis of contract appointments.
  12. Interested candidates who are willing to apply for the post and likely to continue preferably till the completion of the project, may download applications from the ICMR website (www.main.icmr.nic.in). Duly filled application with Recent Photograph along with self-attested copies of all relevant certificates and experience should be brought to Room No 322, Division of ECD, Indian Council of Medical Research, V. Ramalingaswami Bhawan, Ansari Nagar, New Delhi-110029 between 9-11 am on the day of the interview.
    Candidates coming after 11.15 am will not be considered
  13. Incomplete applications, without a photograph or without copies of relevant certificates and applications not in the prescribed format will not be entertained. The Director-General, ICMR reserves the right to increase/decrease the no. of posts or reject the applications or cancel the applications or cancel the notification without assigning any reason thereof.
  14. No TA/DA will be paid for appearing in the interview.
  15. Any canvassing by or on behalf of the candidates or to bring political or outside influence
    with regard to selection/recruitment shall lead to disqualification.
  16. The eligible candidates will be interviewed after verification of essential qualifications and experience on the day of the interview after 11.15 am.
  17. The Selection Committee reserves the right to reduce the experience in the case of deserving candidates.

GENERAL CONDITIONS – The conditions of employment will be the same as that of the
project staff on a contract basis. The candidates have no right to claim any regular employment at this institute.

For any query please contact Mrs Harjeet Kaur Bajaj, Administrative Officer, Division of ECD or Mr. Ramesh Chand, Section Officer, Division of ECD, ICMR-HQ, New Delhi at extension number 259 /284 orat011-26589699

For Post I

Essential Qualifications

  • 1st Class Master Degree in Immunology/ Biotechnology or any equivalent degree from a recognized university with 4 years experience in Biotech/ clinical research related to the development of new diagnostics/drugs/clinical research.
    Or
  • 2nd Class Master’s Degree Immunology/ Biotechnology or any equivalent degree + PhD degree in relevant subjects from a recognized university with 4 years experience related to the development of new diagnostics/drugs/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, working on databases.
  3. Thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial conduct.

Nature of Duties

  • To manage all clinical aspects of the study including assessing operational feasibility and recommending a study execution plan; developing and managing comprehensive study timelines and metrics.
  • The job requires frequent Indian travel to sites for monitoring, quality assurance and quality management for at least 15 days a month.
  • To prepare QA/QC Plan for the sites for all studies and participate in the Selection and management/Oversight of sites, CRO/vendors develop vendor specifications; review vendor reports, budgets and metrics.
  • To provide study-specific training and leadership to Clinical Research Staff, including CROs, CRAs, Sites and other contract personnel.
  • To plan, Execute and Lead study-specific meetings.
  • 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 the study budget and maintain it within financial goals.
  • To manage study files and process or administrative approvals.
  • The job may require travel to the trial sites and attending outstation meetings
  • Any other job assigned by the competent authority.

Consolidated Emoluments – Rs. 57,660/- per month (consolidated) with no other allowances

For Post II

Essential Qualifications

  • 1st Class Master Degree in Biotechnology 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. or any equivalent degree + PhD degree in relevant subjects from a recognized university with 2 years experience in Pharma/Biotech/CRO industry/ Public Health/ Clinical research.

Desirable Qualifications

  1. PhD with at least 2 years post-Doc experience in a biomedical subject,s 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

  • To manage all clinical aspects of the study including assessing operational feasibility and recommending a study execution plan; developing and managing comprehensive study timelines and metrics.
  • To participate in the Selection and management/Oversight of CRO/vendors develop vendor specifications; review vendor reports, budgets and metrics.
  • To provide study-specific training and leadership to Clinical Research Staff, including CROs, CRAs, Sites and other contract personnel.
  • To plan, Execute and Lead study-specific meetings.
  • 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 the study budget and maintain it within financial goals
  • To manage study files and process or administrative approvals.
  • Any other work assigned by the team leader pertaining to ITRC.
  • The job may require travel to the trial sites and attending outstation meetings

Consolidated Emoluments – Rs. 57,660/- per month (consolidated) with no other allowances

For Post III

Essential Qualifications

  • 1st Class Master’s Degree – in Biochemistry/Pharmacology/Bio-Sciences or any equivalent degree from a recognized university with 4 years experience in the CRO industry/Public Health/Clinical research/trials. OR
  • 2nd Class Master’s Degree – in Biochemistry/Bio-Sciences/Life Sciences or any equivalent degree + PhD degree in relevant subjects from a recognized university with 4 years’ experience related to clinical research.

Desirable Qualifications

  1. Ph.D. in Pharmacology with at least 2 years post-Doc 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, working on databases.
  3. Thorough knowledge of New Drug and Clinical Trial Rules 2019 (Schedule Y), GCP, ICH guidelines and regulatory requirements for clinical trial conduct

Nature of Duties

  • To manage all clinical aspects of the study including assessing operational feasibility and recommending a study execution plan; developing and managing comprehensive study timelines and metrics.
  • Job requires frequent all India travel to sites for monitoring, quality assurance
    and quality management for at least 15 days a month.
  • Participate in Selection and management/Oversight of sites, CRO/vendors develops vendor specifications; review vendor reports, budgets and metrics.
  • To provide study-specific training and leadership to Clinical Research Staff, including CROs, CRAs, Sites and other contract personnel.
  • To plan, Execute and Lead study-specific meetings.
  • 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 the study budget and maintain it within financial goals
  • To manage study files and process or administrative approvals.
  • The job may require travel to the trial sites and attending outstation meetings
  • Any other job assigned by the competent authority.

Consolidated Emoluments – Rs. 57,660/- per month (consolidated) with no other allowances

Click here to download the application format

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