Indian Council of Medical Research (ICMR) is an Autonomous Organization, under the Department of Health Research, Ministry of Health & Family Welfare, Govt, of India. ICMR is dealing with biomedical/ health research in various areas, in collaboration with National/ International agencies, through its Headquarters at New Delhi and 27 Institutes/ Centres and a large number of field stations, situated across the country.
Following posts are to be filled purely on contractual basis for working under various projects under ITRC (ECD) ICMR Hqrs, New Delhi, through walk-in Interview on 28th Nov. 2023 at ICMR Hqrs., Delhi
Sr. Consultant - One post (TB Vaccine Trial)
Essential Qualification : • Professional with M.D. or Ph.D. in relevant subject (Life sciences) from recognized Institution with 3-5 years of experience in clinical research/ trial with published papers (preferably). Or • 1st class Master’s degree in life sciences/Medical science from a recognized university with 6-8 yrs of experience in clinical research/trial with published papers (preferably).
Desirable Qualification & Experience : i. Experience in management & monitoring of regulatory Clinical Trials
ii. Able to prepare SOPs, logs, protocols and other documents for trial conduct.
iii. Knowledge of Regulatory Guidelines, New Drug and Clinical Trial Rules 2019 (Schedule Y), GCP, GCLP, ICH guidelines and other regulatory requirements
iv. Experience in managing and maintaining databases for quality systems.
v. Able to undertake site visits across India for monitoring
vi. Able to manage multicentric trial and complete the activities at all trial sites and compile the data ensuring compliance and data query resolutions and support CSR writing
Age Limit : Upper age limit upto 65 years.
Consolidated Emoluments : 1,00,000/-
Tenure : Upto 31st March 2024
Consultant Scientific (Project Manager)- Two posts (TB Vaccine Trial)
Essential Qualification : • 1st Class Master’s Degree or equivalent in Medicine/Bio-Sciences/Life Sciences/Biochemistry /Pharmacology/ Chemistry or any equivalent post from a recognized university with 4 years’ experience in clinical research with published papers (preferably). OR
• 2nd Class M. Sc. In Biochemistry/Bio-Sciences/Life Sciences/ Pharmacology/ Biotechnology/M. Pharm or any equivalent Masters degree + PhD degree in relevant subjects from a recognized university with 2 years’ experience in clinical research with published papers (preferably)
Desirable :
i. At least 2 year post-Doctoral experience in biomedical subject particularly in health research related areas. Working experience in Quality Qualification & Experience: Control/Assurance, Medical writing.
ii. Knowledge of computer applications or business intelligence tools/data management/data synthesis/Report writing, data mining, working on databases.
iii. Thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial conduct.
iv. Able to undertake site visits across India for monitoring and complete the project related work including the support in CSR writing
Age Limit : Upper age limit upto 40 years
Consolidated Emoluments : Rs. 70,000/- per month (consolidated) with no other allowances
Tenure : Upto 31 March 2024.
Place of Work : ICMR Hqrs.
Consultant (Data Management) Fateh TB
Essential Qualification : Essential Qualifications Post Graduate Degree or equivalent (Bioinformatics/ Computer Sciences any related subject) from reputed organization and 5 years of experience in data management preferably in clinical research/clinical trials Or BE/B.Tech Degree in information Technology (IT)/Computer Science (CS) from the recognized Institute /University with 6 years of experience in Data management.
Desirable Qualification & Experience:
• Expertise in PHP and PHP Framework like PDO, Codeigniter, Laravel, etc.
• Proficiency in Scripting languages, jQuery, Ajax etc.
• Expertise in MySQL, Postgresql, MS-SQL, Oracle or equivalent.
• Experience in CMS based web development (Joomla, Drupal, Word Press).
• Excellent knowledge of Database Management Systems.
• Use of commercial and proprietary clinical data management systems, coding dictionaries / encoding systems (e.g. MedDRA, WHODRL), other software in support of data management activities (e.g. SAS, ACCESS, SQL, Oracle) programming skills and experience with electronic data capture.
• Knowledge of implementation of Security policies and to get Security Audit of the developed system.
• Ability to develop and advice on training programs.
• Experience in managing and maintaining databases for quality systems
• Able to undertake site visits across India for monitoring and complete the data queries and prepare tables for the CSR reports
Age Limit : Upper age limit upto 40 years
Consolidated Emoluments : Rs. 1,00,000/-
Tenure : For 1 year
Sr. Consultant - One post (FaTeh TB project)
Essential Qualification : • Professional with M.D. or Ph.D. in relevant subject (Life sciences) from recognized Institution with 5 years of experience in clinical research/ trial with published papers (preferably). Or • 1st class Master’s degree in life sciences/Medical science from a recognized university with 8 yrs. of experience in clinical research/trial with published papers (preferably) Desirable Qualification & Experience :
• Experience in management & monitoring of regulatory Clinical Trials and medical writing
• Able to prepare SOPs, logs, protocols and other documents for trial conduct.
• Knowledge of Regulatory Guidelines, New Drug and Clinical Trial Rules 2019 (Schedule Y), GCP, GCLP, ICH guidelines and other regulatory requirements
• Experience in managing data for quality systems
• Able to undertake site visits across India for site feasibility, monitoring and complete the capacity building of sites for trial and write CSR reports
Age Limit : Upper age limit upto 50 years
Consolidated Emoluments : 1,00,000/-
Tenure : One year
Project Research Scientist II (Non-Medical) (ITRC) (Clinical Operations) – One post
Essential Qualification : 1st Class Master’s Degree in Biotechnology/Clinical Pharmacology/ M. Pharm or any equivalent degree from a recognized university with 3 yrs. experience or Ph.D in CRO industry/ Public Health/clinical research
Desirable Qualification & Experience : i. At least 2 yrs experience in biomedical subject particularly in health research related areas. Working experience in scholarly publications.
ii. Knowledge of computer applications /data management/data synthesis/Report writing, Medical writing data mining, writing articles/ working on databases.
iii. Knowledge of New Drug and Clinical Trial Rules 2019 (Schedule Y), GCP, ICH guidelines and regulatory requirements for clinical trial conduct. iv. Able to undertake site visits across India for monitoring Age Limit : Upper age limit upto 40 years. (Relaxable to OBC and SC/ST Candidate as per Govt. of India)
Consolidated Emoluments : Rs. 67000/- + HRA as admissible
Tenure : Up to March 2024
Consultant (Clinical Research Associate) : One post
Essential Qualification : Post Graduate Degree in Bio-sciences / Biotechnology/ Life Sciences or equivalent with 2 yrs. or more experience in clinical research/trials.
Desirable Qualification and & Experience : i. Experience in handing data of clinical studies and computer applications. ii. Experience in managing clinical research / trial, Medical writing.
iii. Able to prepare safety Able to prepare SOPs, logs etc. for trial conduct, safety listings and Tables iv. Able to prepare SOPs for trial conduct and write safety reports and SAE narratives.
v. Thorough knowledge of New Drug and Clinical Trial Rules 2019, GCP, ICH guidelines and regulatory requirements for clinical trial conduct. vi. Able to undertake site visits across India for monitoring
Age Limit : Upper age limit upto 35 years
Consolidated Emoluments : Rs. 60, 000/- per month (consolidated) with no other allowances
Tenure : For 1 year Place of Work ICMR Hqrs.
Consultant (Clinical Research Coordinator) – Two posts
Essential Qualifications
• Bachelor Degree in any discipline of Life Sciences/ IT /Commerce with 3 or more years relevant experience.
OR
• Post Graduate Degree in Life Sciences/ IT /Commerce with one year or more relevant experience.
Desirable
• Experience in maintaining and handing data and computer applications.
• Knowledge in maintaining trackers for clinical studies.
• Able to prepare SOPs, logs etc. listings and Tables for clinical study reports
• Basic knowledge of administrative and regulatory requirements for clinical studies
Age Limit : Upper age limit upto 35 years
Consolidated Emoluments : Rs.31,000 /- fixed per month
Tenure : For 1 year
Place of Work : ICMR Hqrs
All the deserving candidates who wish to appear for the interview should report on 28/11/2023 along with 5 copies of their Bio-data in Application format given below the advertizement. The candidates must reach at 8.30 AM on 28/11/2023 for registration at ICMR Hqrs. Office, Delhi. The verification of the documents of the candidate will start from 8:30 AM onwards and eligible candidates after verification would be interviewed 10:30 AM onwards. One Candidate can apply for a maximum of 2 posts only and should indicate the names of the posts clearly on application form. Applicants coming after 11.00 AM on 28th Nov. 2023 will not be entertained.
General Terms and conditions: -
1. Number of positions may vary.
2. These positions are meant for temporary projects and co-terminus with the project.
3. Engagement of the above advertised Project Human Resource Positions will depend upon availability of funds, functional requirements and approval of the Competent Authority. Therefore, we are not committed to fill 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/stipend shown in this advertisement are project specific and may vary according to sanction of the funding agency of the Project.
5. Cut-off date for age limit will be as on the date of last date for 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 a latest valid non-creamy layer certificate. PWD candidates shall produce latest disability certificate issued by a Medical board of Government hospital with not less than 40% disability.
8. Separate application should be submitted for each position. Allotment of project to the successful candidates will be decided by the competent authority at its discretion.
9. Qualification & experience should be in 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 / Organizations 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 rights 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 on Project Human Resource Positions cannot be permitted to register for Ph.D., due to time constraints.
16. The persons engaged on 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 on 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 Quartersand other facilities applicable to the regular staff of ICMR etc. are not admissible to the projecthuman resource positions.
18. Successful candidates will normally be engaged on 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 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 application form in the prescribed format with arecent passport size color 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 schedule 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 the website of ICMR regularly for further updates related to this advertisement.
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