Other Jobs- ICMR Project Scientist Recruitment 2022 – ICMR invites applications for recruitment of 14 Project Scientist, Consultant Posts. The walk in selection process will be held on 22 June 2022.

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ICMR

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.

SI No Name of Posts No. of Posts
1. Project Scientist -V (Bio-Statistician/Data Scientist) (Non-Medical) 01
2. Project Scientist Support-II (Medical Affairs and Clinical Development) 01
3. Project Scientist -II (Medical / Clinical Services) (Medical) 01
4. Sr. Consultant (Project Management) 01
5. Consultant (Quality Assurance) 01
6. Consultant (Clinical Research Associate) 03
7. Consultant (Clinical Research Associate) 03
8. Consultant (Clinical research Coordinator) 03
Total 14

Educational Qualification:  

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.

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.

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.

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

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.

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.

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.

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:

1. Project Scientist -V (Bio-Statistician/Data Scientist) (Non-Medical) – Upper age limit upto 40 years.
2. Project Scientist Support-II (Medical Affairs and Clinical Development) – Upper age limit upto 40 years
3. Project Scientist -II (Medical / Clinical Services) (Medical) – Upper age limit upto 40 years
4. Sr. Consultant (Project Management) – Upper age limits up to 70 years
5. Consultant (Quality Assurance) – Upper age limit upto 55 years
6. Consultant (Clinical Research Associate) – Upper age limit upto 55 years
7. Consultant (Clinical Research Associate) – Upper age limit for up to 45 years
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:

1. Project Scientist -V (Bio-Statistician/Data Scientist) (Non-Medical) – Rs. 57,660/- Fixed Per month
2. Project Scientist Support-II (Medical Affairs and Clinical Development) – Rs. 72,325/- Fixed Per month
3. Project Scientist -II (Medical / Clinical Services) (Medical) – Rs. 72,325/- Fixed Per month
4. Sr. Consultant (Project Management) – Rs. 1,00,000/- Fixed Per month
5. Consultant (Quality Assurance) – Rs. 1,00,000/- Fixed Per month
6. Consultant (Clinical Research Associate) – Rs. 60,000/- Fixed Per month
7. Consultant (Clinical Research Associate) – Rs. 31,000/- Fixed per month
8. Consultant (Clinical research Coordinator) – Rs. 31,000/- Fixed per month

Selection Process:

ICMR may follow the following process to select the candidates.

1. Interview

How to apply:  

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: 

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
Date: 22.06.2022
Time: 8.30 am onwards till 10:30 AM.

View Notification

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