ICMR Recruitment 2023 for Project Research Scientist

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ICMR Recruitment 2023: The Indian Council Of Medical Research has announced an online recruitment application for the Consultants/Project Research Scientist post. There are 11 vacancies to be filled for this recruitment. Interested candidates who completed a B.E/B.Tech/MBBS/MPH/MD/MS/DNB/B.Sc/M.Sc/PhD/PG degree can apply for this job. Eligible candidates can apply online on or before 28 November 2023. The detailed eligibility and selection process of ICMR Recruitment are given below.

ICMR: The Indian Council of Medical Research, the apex body in India for the formulation, coordination, and promotion of biomedical research, is one of the world’s oldest and largest medical research bodies. The ICMR has come a long way since it was known as the IRFA, but the Council is conscious that it still has miles to go in pursuit of scientific achievements and health targets.

Table of Contents

ICMR Recruitment 2023:

ICMR Walk-in-interview 2023 Consultants/Project Research Scientist:

Job Role	Consultants/Project Research Scientist
Qualification	B.E/B.Tech/MBBS/MPH/MD/MS/DNB/B.Sc/M.Sc/PhD
Job Type	Central Govt Jobs
Total Vacancies	10 Posts
Salary	Rs. 31,000-1,00,000/-
Experience	Experienced
Job Location	New Delhi
Interview Date	28 November 2023

Detailed Eligibility of ICMR Recruitment:

Educational Qualification:

Sr. Consultant (TB Vaccine Trial):

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:
- Experience in management & monitoring of regulatory Clinical Trials
- 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 and maintaining databases for quality systems.
- Able to undertake site visits across India for monitoring
- 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

Consultant Scientific (Project Manager) (TB Vaccine Trial):

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 Qualification & Experience:
- At least 2 year post-Doctoral experience in biomedical subject particularly in health research related areas. Working experience in Quality
  Control/Assurance, Medical writing.
- Knowledge of computer applications or business intelligence tools/data management/data synthesis/Report writing, data mining, working on databases.
- Thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial conduct.
- Able to undertake site visits across India for monitoring and complete the project related work including the support in CSR writing

Consultant Scientific (Medical Project Coordinator) (Saharia TB project):

Post Graduate Degree (MD/MS/DNB) after MBBS with one year experience with published papers (preferably) OR
Postgraduate Diploma in Medical subjects after MBBS with two years experience with published papers (preferably) OR
MBBS degree with 4 years’ experience in clinical research after MBBS with published papers (preferably)
Desirable Qualification & Experience:
- Master’s degree in the relevant subject (Community Medicine/Preventive & Social Medicine/ Paediatrics/ Medicine/ Tropical Medicine/Microbiology/Community Medicine/ Public Health) from a recognized university.
- Thorough knowledge of New Drug and Clinical Trial Rules 2019 (Schedule Y), GCP, ICH guidelines and regulatory requirements for clinical trial conduct.
- Knowledge of Computer Applications & Data Management.
- Able to undertake site visits across India for monitoring and complete the project related work including the support in report writing

Consultant (Data Management) Fateh TB:

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.
- se 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 implementing Security policies and getting a 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

Sr. Consultant – (FaTeh TB project):

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

Project Research Scientist II (Non-Medical) (ITRC) (Clinical Operations):

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:
- At least 2 yrs experience in biomedical subject particularly in health research related areas. Working experience in scholarly publications.
- Knowledge of computer applications /data management/data synthesis/Report writing, Medical writing data mining, writing articles/ working on databases.
- Knowledge of New Drug and Clinical Trial Rules 2019 (Schedule Y), GCP, ICH guidelines and regulatory requirements for clinical trial conduct.
- Able to undertake site visits across India for monitoring

Project Research Scientist II (Medical) (Medical Affairs & Clinical Development) (ITRC):

MBBS degree with 4 years experience in clinical research after MBBS OR
MBBS with MPH/Ph.D 4 years experience in clinical research after MBBS OR
MBBS + PG degree including integrated PG degrees in clinical research after MBBS
Desirable Qualification & Experience:
- Thorough knowledge of New Drug and Clinical Trial Rules 2019 GCP, ICH guidelinesand regulatory requirements for clinical trial conduct.
- Additional Post-doctoral research/ teaching experience in relevant subjects in recognized institute(s).
- Knowledge of Medical writing, writing safety reports and SAE
- Contribute to implementation of clinical protocol and facilitate completion of clinical study reports
- Ensure Monitoring of safety and adverse events for projects under development.
- Able to undertake site visits across India for monitoring

Consultant (Clinical Research Associate):

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:
- Experience in handing data of clinical studies and computer applications.
- Experience in managing clinical research / trial, Medical writing.
- Able to prepare safety Able to prepare SOPs, logs etc. for trial conduct, safety listings and Tables
- Able to prepare SOPs for trial conduct and write safety reports and SAE narratives.
- Thorough knowledge of New Drug and Clinical Trial Rules 2019, GCP, ICH guidelines and regulatory requirements for clinical trial conduct.
- Able to undertake site visits across India for monitoring

Consultant (Clinical Research Coordinator):

Bachelor Degree in any Life Sciences/ IT /Commerce discipline 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(As on 28 November 2023):

Sr. Consultant(TB Vaccine Trial): 65 Years
Consultant Scientific (Project Manager): 40 Years
Consultant Scientific (Medical Project Coordinator): 50 Years
Consultant (Data Management): 40 Years
Sr. Consultant – (FaTeh TB project): 50 Years
Project Research Scientist II (Non-Medical):
Project Research Scientist II (Medical): 40 Years
Consultant (Clinical Research Associate): 35 Years
Consultant (Clinical Research Coordinator): 35 Years

Age Relaxation: Age relaxation will be as per the guidelines of ICMR

Salary:

Sr. Consultant(TB Vaccine Trial): Rs. 1,00,000/-
Consultant Scientific (Project Manager): Rs. 70,000/-
Consultant Scientific (Medical Project Coordinator): Rs. 1,00,000/-
Consultant (Data Management): Rs. 1,00,000/-
Sr. Consultant – (FaTeh TB project): Rs. 1,00,000/-
Project Research Scientist II (Non-Medical): Rs. 67000+ HRA
Project Research Scientist II (Medical): Rs. 80,000+ HRA
Consultant (Clinical Research Associate): Rs. 60, 000/-
Consultant (Clinical Research Coordinator): Rs.31,000 /-

Total Vacancies: 10 Posts

Sr. Consultant(TB Vaccine Trial): 01 Post
Consultant Scientific (Project Manager): 02 Posts
Consultant Scientific (Medical Project Coordinator): 01 Post
Sr. Consultant – (FaTeh TB project): 01 Post
Project Research Scientist II (Non-Medical): 01 Post
Project Research Scientist II (Medical): 01 Post
Consultant (Clinical Research Associate): 01 Post
Consultant (Clinical Research Coordinator): 02 Posts

Selection Process:

The selection process includes Interviews.

How to apply for ICMR Recruitment 2023?

All interested and eligible candidates who can appear for the interview should report at the mentioned address along with 5 copies of their Bio-data in the Application format given below on 28 November 2023. at 8.30 am.

For More Details & Application Form: Click here.

Interview Date: 28 November 2023

Time: 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

Venue:

ICMR Hqrs. Office,
Delhi

Documents to be Submitted

Recent passport-size color photograph along with a detailed bio-data/C.V.
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

ICMR Recruitment 2023 Project Research Scientist:

Job Role	Project Research Scientist
Qualification	M.Sc/PG degree
Job Type	Central Govt Jobs
Total Vacancies	01 Post
Salary	As per ICMR norms
Experience	Experienced
Job Location	New Delhi
Last Date	21 November 2023

Detailed Eligibility – ICMR Recruitment:

Educational Qualification:

Project Research Scientist- I (Non-Medical):

First Class Post Graduate Degree, including the integrated PG Degrees in relevant subjects (Science/Public Health/Life Sciences/ Psychology)
Second Class Post Graduate Degree, including the integrated PG Degrees with PhD (Science/Public Health/Life Sciences/ Psychology)

Desirable Qualification:

Candidate with knowledge and technical experience in Public Health. Candidate may be required to do field visits as per requirement.
Experience working in the field and managing multicentric projects in government institutes will be an added advantage.
Candidate has at least two research/review papers published in UGC-recognized journals.

Job Requirement:

The candidate must coordinate with the Institute/other Centers selected under this call for proposal and monitoring of the work under multicentric projects and assist the Program officer in reviewing the data collected and preparing reports and any other work assigned by the Program Officer.

Duration: 01 Years

Age Limit(As on 21 November 2023): 35 Years

Age Relaxation: Age relaxation will be as per the guidelines of ICMR.

Total Vacancies: 01 Post(UR)