ICMR
Project Scientist Recruitment 2022 | ICMR: 14 Project Scientist Posts 2022 | ICMR
Project Scientist Job Notification 2022 | ICMR Project Scientist 2022
Application Form PDF Download @ https://main.icmr.nic.in/– ICMR invites
applications for recruitment of 14 Project Scientist, Consultant Posts. The
applicants are requested to Download Application Form through Official Website
@ https://main.icmr.nic.in/.
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ICMR Recruitment 2022 [Quick Summary] |
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Organization Name: |
Indian Council Of Medical Research |
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Notification No: |
ITRC/ECD/1/2022 |
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Job Category: |
Central Govt Jobs |
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Employment Type: |
Regular Basis / Contract Basis / Temporary Basis |
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Total No of Vacancies: |
14 Project Scientist, Consultant Posts |
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Place of Posting: |
New Delhi |
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Walk in Date: |
22nd June, 2022, 10:30 A.M. |
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Apply Mode: |
Offline |
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Official Website |
https://main.icmr.nic.in/ |
Latest
ICMR Project Scientist Vacancy Details:
Name of the Post & No of Vacancies:
ICMR
intends to engage following Non-Institutional project human resource positions,
purely on temporary contract basis for its short-term research projects, being
undertaken at Division of Epidemiology and Communicable Diseases (ECD)
(Unit-Tuberculosis, Leprosy and Tribal Health), ICMR Hqrs, New Delhi.
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SI No |
Name of Posts |
No. of Posts |
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1. |
Project Scientist -V (Bio-Statistician/Data Scientist) (Non-Medical) |
01 |
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2. |
Project Scientist Support-II (Medical Affairs and Clinical Development) |
01 |
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3. |
Project Scientist -II (Medical / Clinical Services) (Medical) |
01 |
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4. |
Sr. Consultant (Project Management) |
01 |
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5. |
Consultant (Quality Assurance) |
01 |
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6. |
Consultant (Clinical Research Associate) |
03 |
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7. |
Consultant (Clinical Research Associate) |
03 |
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8. |
Consultant (Clinical research Coordinator) |
03 |
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Total |
14 |
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ICMR Project Scientist Eligibility Criteria:
Educational
Qualification:
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1. Project
Scientist -V (Bio-Statistician/Data Scientist) (Non-Medical) - Essential: - 1st Class Post Graduate Degree (Biostatistics /Statistics, M.Tech/MCA
– Data Scientist/ Computer Science or equivalent) from reputed organization
and 3 years of experience in data management preferably in clinical
research/clinical trials. OR - 2nd Class Post Graduate Degree (Biostatistics / Statistics,
M.Tech/MCA – Data Scientist/ Computer Science or equivalent) from reputed
organization with Ph.D. in relevant subject with 3 years of relevant
experience with published research papers. Desirable: i. Knowledge of data management and SPSS. ii. Ability to develop and advice on training programs. Experience of
Data Management in multicentric clinical trials/studies specially drug
trials/vaccine trials. iii.Experience in handling clinical trial data-base. iv. Experience in data-cleaning, raising database queries, query
resolution. Experience in handling and monitoring eCRF based studies.
Experience in statistical analysis and preparation of report. |
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2. Project
Scientist Support-II (Medical Affairs and Clinical Development) - Essential: - Post Graduate Degree (MD/MS/DNB) after MBBS with one year experience.
OR - Postgraduate Diploma in Medical subjects after MBBS with two years’
experience OR - MBBS degree with 4 years’ experience in clinical research after MBBS Desirable: i. Master degree in the relevant subject (Community Medicine/
Preventive & Social Medicine/ Paediatrics/ Medicine/ Tropical Medicine/
Microbiology/Pharmacology/Community Health Administration/Health
Administration/ Family Medicine/ Epidemiology/ Public Health) from a
recognized university. ii. Thorough knowledge of New Drug and Clinical Trial Rules 2019
(Schedule Y), GCP, ICH guidelines and regulatory requirements for clinical
trial conduct. iii. Additional Post-doctoral research/teaching experience in relevant
subjects in recognized institute(s). Knowledge of Computer Applications or
Business Intelligence tools /Data Management. |
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3. Project
Scientist -II (Medical / Clinical Services) (Medical) – Essential: -Post Graduate Degree (MD/MS/DNB) after MBBS with one year experience
in clinical research OR -Postgraduate Diploma in Medical subjects after MBBS with two years’
experience. - MBBS degree with 4 years of experience, preferably in clinical
research/trial after MBBS Degree. Desirable: i. Experience in conducting Vaccine/drug trial/clinical research
/Clinical Management. ii. Able to prepare safety
reports and ensure the timely management and reporting of AEs and SAEs by
sites by supporting them iii. Experience in managing and maintaining databases for quality
systems. iv. Able to prepare SOPs for trial conduct and write safety reports and
SAE narratives. Knowledge of New Drug and Clinical Trial Rules 2019 (Schedule
Y), GCP, ICH guidelines and other regulatory requirements for clinical trial
conduct. |
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4. Sr.
Consultant (Project Management) – Essential: - Professional with M.D. or Ph.D. (Medical Pharmacology/Medical
Microbiology/Public health/Life Sciences/Biotechnology/Biosciences) in
relevant subject from recognized Institution and published papers with 10
years of experience in clinical research/clinical trials with published
papers. OR - Retired Government employees with requisite educational qualification
of MD/Ph.D in Life Sciences with 10 years of experience in clinical
research/clinical trial (related to TB research) drawing pay in pay band of
Rs.15,600/-39100+grade pay of Rs.6600/-at the time of retirement Desirable: I. Experience in management and monitoring of regulatory Clinical
Trials and Biomedical Research. II. Able to prepare SOPs, logs, protocols and other related 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 for clinical trial conduct. IV. Experience in managing and maintaining databases for quality systems |
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5. Consultant
(Quality Assurance) - Essential: Professionals with MD with 2 years’ experience in quality assurance of
clinical research/trial with published papers OR or 1st Class Masters M.
Tech. in Biotechnology/ M. Pharma/ M.Sc. in Pharmacology/ Clinical
Research/Biochemistry/Chemistry/Bioscie nces with Ph.D. in relevant subject
with 2 years’ experience of Quality Assurance in Clinical Studies with
published papers. i. Desirable: Experience in monitoring/Quality Assurance for conducting Vaccine/drug
trial/clinical research /Clinical Management. ii. Evaluating quality events,
incidents, queries and complaints, handling compliance issues. iii.
Experience in managing and maintaining databases for quality systems.
Knowledge of regulatory New Drug and Clinical Trial Rules 2019 (Schedule Y),
GCP, ICH guidelines and other regulatory requirements for clinical trial
conduct. |
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6. Consultant
(Clinical Research Associate) – Essential: - 1st Class Master Degree in Life sciences/Biotechnology/Bio-Medical
sciences/M.Pharm or any equivalent degree from a recognized university with 4
years’ experience or BAMS/BHMS/BDS/BV.Sc or any equivalent degree from a
recognized university with 5 years’ experience in Biotech/clinical research
related to 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’ experience related to clinical research. Desirable: i. Ph.D. with 2 years post-Doctoral experience in biomedical subject
particularly in health research related areas. Working experience in Quality
Control/Assurance. ii. 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. |
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7. Consultant
(Clinical Research Associate) – Essential: - 1st Class Master Degree in Life sciences/Biotechnology/Bio-Medical
sciences/M.Pharm or any equivalent degree from a recognized university with 4
years’ experience or BAMS/BHMS/BDS/BV.Sc or any equivalent degree from a
recognized university with 5 years’ experience in Biotech/clinical research
related to 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’ experience related to clinical research. Desirable: i.Ph.D. with 2 years post-Doctoral experience in biomedical subject
particularly in health research related areas. Working experience in Quality
Control/Assurance. ii. 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. |
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8. Consultant
(Clinical research Coordinator) – Essential: - Professional having M.Sc in Biomedical sciences or B.Tech (Comp.
Sceience, 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: -Post graduate degree in relevant subjects - Knowledge of computer applications or business intelligence
tools/data management/data synthesis/Report writing, data mining, working on
databases. |
Age Limit:
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1. Project
Scientist -V (Bio-Statistician/Data Scientist) (Non-Medical) - Upper age limit upto 40 years. |
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2. Project
Scientist Support-II (Medical Affairs and Clinical Development) - Upper age limit upto 40 years |
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3. Project
Scientist -II (Medical / Clinical Services) (Medical) - Upper age limit upto 40 years |
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4. Sr.
Consultant (Project Management) - Upper age limits up to 70 years |
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5. Consultant
(Quality Assurance) - Upper age limit upto
55 years |
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6. Consultant
(Clinical Research Associate) - Upper age
limit upto 55 years |
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7. Consultant
(Clinical Research Associate) - Upper age
limit for up to 45 years |
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8. Consultant
(Clinical research Coordinator) - Upper age limit for up to 45 years |
Candidates
Relaxation in Upper Age limit will be provided as per Govt. Rules. Go through ICMR
official Notification 2022 for more reference
Salary Details:
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1. Project
Scientist -V (Bio-Statistician/Data Scientist) (Non-Medical) - Rs. 57,660/- Fixed Per month |
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2. Project
Scientist Support-II (Medical Affairs and Clinical Development) - Rs. 72,325/- Fixed
Per month |
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3. Project
Scientist -II (Medical / Clinical Services) (Medical) - Rs. 72,325/- Fixed
Per month |
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4. Sr.
Consultant (Project Management) - Rs. 1,00,000/-
Fixed Per month |
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5. Consultant
(Quality Assurance) - Rs. 1,00,000/- Fixed Per month |
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6. Consultant
(Clinical Research Associate) - Rs. 60,000/- Fixed Per month |
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7. Consultant
(Clinical Research Associate) - Rs. 31,000/- Fixed per month |
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8. Consultant
(Clinical research Coordinator) - Rs. 31,000/- Fixed
per month |
ICMR Project Scientist Selection Process 2022:
ICMR may follow the
following process to select the candidates.
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1. |
Interview |
How to apply
for ICMR Project Scientist Post:
Eligible Candidates advised to
Download and read ICMR Job notification to get aware of recruitment schedule
and venue from official website ICMR. Candidate must reach advertised venue
(Address & Walk in Date Mentioned in Official Notification) with all
original document and Xerox copies, filled in application form (if required)
Important Dates
for ICMR Project Scientist Post:
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Venue: |
All the
candidates who wish to appear for the interview should report at Reception,
ICMR HQ, V Ramalinga swami Bhawan, Ansari Nagar, New Delhi |
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Date: |
22.06.2022 |
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Time: |
8.30 am
onwards till 10:30 AM. |
ICMR Project
Scientist Official Notification & Application Link:
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ICMR Official Website
Career Page |
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ICMR Official
Notification & Application Form PDF |
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