ICMR-ICMR
Consultant Recruitment 2023 | ICMR-ICMR Consultant Job Notification 2023 | ICMR-ICMR
Consultant 2023 Application Form PDF Download @ https://main.icmr.nic.in/– ICMR-ICMR
invites applications for recruitment of 12 Consultant, Project Scientist, Sr.
Project Manager Posts. The applicants are requested to Download Application
Form through Official Website @ https://main.icmr.nic.in/.
ICMR-ICMR Recruitment 2023 [Quick Summary]
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Organization Name: |
ICMR-National Institute of Medical Statistics |
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Notification No: |
ITRC/ECD/1/2023 |
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Job Category: |
Central Govt Jobs |
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Employment Type: |
Contract Basis |
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Total No of Vacancies: |
12 Consultant, Project Scientist, Sr. Project
Manager Posts |
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Place of Posting: |
Delhi |
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Walk in Date: |
05.04.2023 |
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Apply Mode: |
Offline |
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Official Website |
https://main.icmr.nic.in/ |
Latest
ICMR-ICMR Consultant Vacancy Details:
ICMR-ICMR
Invites Applications for the Following Posts
|
SI No |
Name of
Posts |
No. of Posts |
|
1. |
Consultant Scientific (Project manager ) (For TB Vaccine Trial) |
01 |
|
2. |
Project Scientist Support-II (Medical Affairs and Clinical Development)
(For ITRC) |
01 |
|
3. |
Consultant (Clinical Services) (Medical) (For TB Vaccine Trial) |
01 |
|
4. |
Consultant (Audit) – For TB vaccine trial |
01 |
|
5. |
Sr. Project Manager (For TB vaccine Trial) |
01 |
|
6. |
Consultant (Data Management) |
01 |
|
7. |
Consultant (Clinical Research Coordinator) |
02 |
|
8. |
Project Scientist Support-V (Clinical Operations) (For ITRC) |
01 |
|
9. |
Consultant Scientific (Project Coordinator) (For Tribal TB Project) |
01 |
|
10. |
Consultant Scientific (Medical (Project Coordinator) (For Mission Mode
Saharia TB project) |
01 |
|
11. |
Consultant Scientific (Non-Medical) (Project Coordinator) (For Mission
Mode Saharia TB project) |
01 |
|
|
Total |
12 |
ICMR-ICMR Consultant Eligibility Criteria:
Educational
Qualification: (
|
1. Consultant
Scientific (Project manager ) (For TB Vaccine Trial) - Essential Qualifications: Professional with Masters in
life sciences in relevant subject from recognized Institution with 4-6 years
of demonstrated experience in clinical research/clinical trials with
published papers Desirable
Qualifications: I. Experience in
management and monitoring of clinical Research. II Able to prepare SOPs,
logs, protocols and other related documents for trial conduct. III CRA
experience Program IV Accountable for performance of the studies as per
protocol quality standards and review monitoring Units. V Identify and
escalate training needs/internal management as needed. |
|
2. Project
Scientist Support-II (Medical Affairs and Clinical Development) (For ITRC) - Essential
Qualifications: 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
Qualifications: i. Master degree in
the relevant subject (Community Medicine/ Preventive &Social Medicine /
Pediatrics’ /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 GCP, ICH guidelines and
regulatory requirements for clinical trial conduct. iii. Additional
Post-doctoral research/ teaching experience in relevant subjects in
recognized institute(s). iv. Knowledge of writing safety reports and SAE v.
Contribute to implementation of clinical protocol and facilitate completion
of clinical study reports vi. Ensure Monitoring of safety and adverse events
for projects under development. |
|
3. Consultant
(Clinical Services) (Medical) (For TB Vaccine Trial) - Essential Qualifications: Post Graduate Degree (MD/MS/DNB)
after MBBS with 2 years experience in clinical research with published papers
OR Postgraduate Diploma in Medical subjects after MBBS with 4 years’
experience with published papers Desirable
Qualifications: i. Experience in
conducting Vaccine/drugtrial/clinical research/Clinical Management. ii. Ablet
opreparesafetyreportsaden surethetimely 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. v. Knowledge Of New Drug And
Clinical Trial Rules2019, GCP,ICH guidelines and other regulatory
requirements for clinical trial conduct |
|
4. Consultant
(Audit) – For TB vaccine trial - Essential
Qualifications: Retired Government
employee with Bachelor degree in any discipline drawing pay in the Grade Pay
of Rs. 5400/- and above at time of retirement and having at least 10 years’
work experience in the administration, finance and accounts matters. Desirable
Qualifications: Proficiency in the latest
Accounting packages and Knowledge of MS Office (Word, Power Point, Excel)
along with latest version of Tally. |
|
5. Sr.
Project Manager (For TB vaccine Trial) - Essential
Qualifications: Masters in Life sciences with
6-8 years of research experience including demonstrated core experience in
managing/monitoring of regulatory clinical trials from reputed Institutions
OR 2nd class Masters in life sciences with Ph.D and 3-5 years of post Ph.D
experience with demonstrated core experience in managing/monitoring of
regulatory clinical trials specially Vaccine/drug trial from reputed
Institutions. Desirable
Qualifications: Desirable - Lead cross functional study team for development and execution of
clinical trials. - Develop and maintain Project management Plan (PMP) - Prepare clinical study reports - Thorough knowledge of New clinical trial guidelines, GCP, GCLP, ICH
guidelines and regulatory requirements for clinical trial - Strong written and verbal communication skills - Problem solving skills - Monitor project metrics and prepare required updates to ensure smooth
conduct of the trial. |
|
6. Consultant
(Data Management) - Essential Qualifications: Post Graduate Degree or equivalent (Bioinformatics/ Computer
Sciences/any related subject) from reputed organization and Ph.D. in relevant
subject with 3 years of experience in data management preferably in clinical
research/clinical trials OR 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 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. |
|
7. Consultant
(Clinical Research Coordinator) - Essential
Qualifications: Bachelor Degree in
any discipline of Bio-sciences / Biotechnology/ Life Sciences or equivalent
with 3 years relevant experience. OR Post Graduate Degree in Bio-sciences /
Biotechnology/ Life Sciences or equivalent. Desirable - Experience in handing database and computer applications. - Experience in conducting Vaccine/drug trial/clinical research
/Clinical Management. - 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. |
|
8. Project
Scientist Support-V (Clinical Operations) (For ITRC) - Essential
Qualifications: 1st Class Master Degree in
Biotechnology/Clinical Pharmacology/ M. Pharm/life sciences 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. / M.
Pharm or any equivalent degree + PhD degree in Biotechnology/Pharmacology/ M.
Pharm Life sciences from a recognized university with 2 years’ experience in
Pharma /Biotech/CRO industry/ Public Health/ Clinical research. Desirable
Qualifications: - Experience in Protocol writing, Monitoring the clinical trial and
ensure timely completion of targets - Monitoring project data, eCRFs data entry and query resolution. - Monitor site performance for project targets, and project staff for
patient compliance - Monitor conduct of processes contributing to the performance of a
clinical trial and provide guidance to study sites. - Prepare annual reports of projects and quality trending reports. - Prepare weekly site wise and consolidated site report regarding enrollment
/FU data for targets vs achievement. |
|
9. Consultant
Scientific (Project Coordinator) (For Tribal TB Project) - Professional with Ph.D in Anthropology/Social Science from recognized
Institution and good publication record with 12-15 years of relevant
experience in community work/clinical research/qualitative research Desirable - Experience in planning and executing field studies. - Experience in qualitative software - Lead cross functional study team for execution of multicentric field
study. - Develop and maintain Project management Plan (PMP) - Develop community engagement Plan. Knowledge of computer applications
/Report writing, data management, |
|
10. Consultant
Scientific (Medical (Project Coordinator) (For Mission Mode Saharia TB
project) - Professional with M.D/DNB or
Ph.D after MBBS from recognized Institution and good publication record with
3-5 years of relevant experience in community work and community public
health - Experience in planning and executing/community studies, field
intervention Public Health studies. - Independently initiating and handling research projects in the
related areas - Good clinical experience in managing public health, patient
management in field - Able to conduct telemedicine and coordinate with experts in relevant
areas for the telemedicine - Knowledge of computer applications /data management/Report writing,
data mining, working on databases |
|
11. Consultant
Scientific (Non-Medical) (Project Coordinator) (For Mission Mode Saharia TB
project) - Professional with Ph. D. (Public
health/Life Sciences) fromrecognized Institution and good publication record
with minimum 8- 10 years of relevant experience in clinical studies/field
studies Desirable - Experience in conducting, planning and executing/community studies,
field intervention studies specially in area of TB. - Experience in managing and maintaining data base of research projects
in area of TB. - Independently executing and handling field research projects - Lead cross functional study team for execution of multicentric field
study. - Develop and maintain Project management Plan (PMP) - Develop community engagement Plan. - Knowledge of computer applications /Report writing, data management,
Knowledge of computer applications /data management/Report writing, data
mining, working on databases. |
Age Limit:
|
1. Consultant
Scientific (Project manager ) (For TB Vaccine Trial) - Upper age limit for up to 65 Years |
|
2. Project
Scientist Support-II (Medical Affairs and Clinical Development) (For ITRC) - Upper age limit for up to 40 Years |
|
3. Consultant
(Clinical Services) (Medical) (For TB Vaccine Trial) - Upper age limit for up to 65 Years |
|
4. Consultant
(Audit) – For TB vaccine trial - Upper age
limit for up to 70 Years |
|
5. Sr.
Project Manager (For TB vaccine Trial) - Upper age limit for up to 70 Years |
|
6. Consultant
(Data Management) - Upper age limit for
up to 70 Years |
|
7. Consultant
(Clinical Research Coordinator) - Upper age limit for up to 35 Years |
|
8. Project
Scientist Support-V (Clinical Operations) (For ITRC) - Upper age limit for up to 40 Years |
|
9. Consultant
Scientific (Project Coordinator) (For Tribal TB Project) - Upper age limit for up to 70 years |
|
10. Consultant
Scientific (Medical (Project Coordinator) (For Mission Mode Saharia TB
project) - Upper age limit for up to 55
years |
|
11. Consultant
Scientific (Non-Medical) (Project Coordinator) (For Mission Mode Saharia TB
project) - Upper age limit for up to 55
years |
The Upper age limit is relaxed by 5 years for
SC/ST; 3 years for OBC, 10 Years for Persons with Disabilities (15 years for
SC/ST PWD’s & 13 years for OBC PWD’s) and for Ex-S as per Govt. of India
rules. Candidates Relaxation in Upper Age limit will be provided as per Govt.
Rules. Go through ICMR-ICMR official Notification 2023 for more reference
Salary Details:
|
1. Consultant
Scientific (Project manager ) (For TB Vaccine Trial) - Rs. 70,000/- Fixed Per month |
|
2. Project
Scientist Support-II (Medical Affairs and Clinical Development) (For ITRC) - Rs. 72,325/- Fixed
per month |
|
3. Consultant
(Clinical Services) (Medical) (For TB Vaccine Trial) - Rs. 80,000/- Fixed
Per month |
|
4. Consultant
(Audit) – For TB vaccine trial - Rs. 50,000/- per month |
|
5. Sr.
Project Manager (For TB vaccine Trial) - Rs. 1,00,000/-
fixed per month |
|
6. Consultant
(Data Management) - Rs. 1,00,000/- fixed per month |
|
7. Consultant
(Clinical Research Coordinator) - Rs.31,000 /- fixed per month |
|
8. Project
Scientist Support-V (Clinical Operations) (For ITRC) - Rs. 57,660/- Fixed per month |
|
9. Consultant
Scientific (Project Coordinator) (For Tribal TB Project) - Maximum Upto Rs. 100,000/- per month consolidated |
|
10. Consultant
Scientific (Medical (Project Coordinator) (For Mission Mode Saharia TB
project) - Maximum Upto Rs. 100,000/- per
month consolidated |
|
11. Consultant
Scientific (Non-Medical) (Project Coordinator) (For Mission Mode Saharia TB
project) - Maximum Upto Rs. 100,000/- per
month consolidated |
ICMR-ICMR Consultant Selection Process 2023:
ICMR-ICMR may follow the
following process to select the candidates.
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1. Interview |
|
2. Personal
Discussion |
How to apply
for ICMR-ICMR Consultant Post:
Interested and eligible
candidates possessing the aforementioned Essential Qualification only may
appear for Walk-in-Interview in the Institute with all Original and
self-attested copies of all certificate/testimonials and valid identity proof (Voter
ID card/ PAN Card/Driving License/Passport/Aadhar Card) and one passport size
photograph. No candidate will be allowed to appear in the Interview without the
Original Certificates.
Important Dates
for ICMR-ICMR Consultant Post:
|
Venue: |
ICMR Hqrs.,
ICMR-NIMS building |
|
Walk in
Date: |
The candidates must reach before 10:30 AM on 05/04/2023 at 8.30 AM
till 10:30 AM for registration in ICMR-ICMR. |
ICMR-ICMR Consultant
Official Notification & Application Link:
|
ICMR-ICMR Official
Website Career Page |
|
|
ICMR-ICMR Official
Notification PDF |
|
|
ICMR-ICMR Application
Form PDF |