ICMR Recruitment 2023 12 Consultant Posts

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]

Organization Name:

ICMR-National Institute of Medical Statistics

Notification No:

ITRC/ECD/1/2023 

Job Category:

Central Govt Jobs 

Employment Type:

Contract Basis

Total No of Vacancies: 

12 Consultant, Project Scientist, Sr. Project Manager Posts

Place of Posting: 

Delhi 

Walk in Date: 

05.04.2023 

Apply Mode:

Offline

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.

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

Click Here

ICMR-ICMR Official Notification PDF

Click Here

ICMR-ICMR Application Form PDF

Click Here

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