ICMR Delhi Biotech & Biochem Scientist Jobs – Rs. 57,000 pm Pay

ICMR Delhi Vacancies For Biotech & Biochem – Applications Invited

ICMR Delhi Vacancies For Biotech & Biochem – Applications Invited. MSc/PhD Biotechnology & Biochemistry Project Scientist Job Openings at ICMR New Delhi. Interested and eligible applicants can check out all of the details on the same below:

This Job Expires In :

 

NOTIFICATION FOR THE PROJECT POSTS

Advertisement No. 1/2021

Interested candidates for the position mentioned below are requested to send out the application in the prescribed format only along with updated Bio-Data and also one passport size photograph up to 05:30 PM of 25th March 2021by email at [email protected]. Applicants making an application for more than one post must apply separately. Applicants are additionally asked to fill up the details in the attached Excel sheet likewise. Late received applications will not be entertained. The list of qualified shortlisted applicants will be displayed on the ICMR web site and also shortlisted applicants would be informed telephonically or via email (provided in CV) for the interview. A link to join for an interview through Video Conference will be shared with shortlisted candidates by e-mail.

An interview would certainly be held via Webex/VC/ on 30th & 31st

March. 2021 from 10.00 AM onwards. The candidate will certainly be asked to join the internet link Web-Link for the interview concerning thirty minutes prior to the start of the interview.

NOTE: All the posts are open to all caste categories

Post I

Name of the Post: Project Scientist Support-V (Clinical Operations)

Number of positions: One

Age limit: 40 years. (Relaxable to OBC and also SC/ST Candidate as per Govt. of
India).

Tenure: Upto 31st March 2022. May continue for an additional year based on the performance evaluation report.

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Post II

Name of the Post: Project Scientist Support-V (Clinical Coordinator/QC)

Number of positions: One

Age limit: 40 years. (Relaxable to OBC and also SC/ST Candidate as per Govt. of
India).

Tenure: Upto 31st March 2022. May continue for an additional year based on the performance evaluation report.

How to apply:

1. Departmental candidates or candidates working/have worked on projects of ICMR Institutes/Centre’s shall be given age relaxation to a minimum of five (5) years or a completed months/year based on an earlier project service, whichever is less, they meet the essential qualification and also experience prescribed for the post, with a view to providing the opportunity to compare to other applicants.
2. Age relaxation against post earmarked for reserved candidates will certainly be based on the Govt. of India Norms. No relaxation will be allowed in unreserved posts.
3. Qualification and experience ought to be in a pertinent discipline/field as well as from a reputed institution/organization recognized by the relevant authority. Experience shall count from the date of completion of the minimum educational qualification.
4. Submission of incorrect or false information during the process of personal discussion and/or video conferencing shall disqualify the candidature at any stage.
5. Mere fulfilling the essential qualification/ experience does not guarantee selection.
6. Candidates employed in Govt. Service/ Semi Govt. Autonomous Bodies of State/ Central Govt. should send a” No Objection Certificate” from their employer.
7. The above post is contractual for the duration offered may or may not be renewed subject to satisfactory performance and requirement.
8. Age will be reckoned from the last date of receipt of application.
9. This post is purely short-term and co-terminable with the project. Employees will be on a consolidated pay basis.
10. The appointment will certainly be made on the basis of the results of personal discussions and/ or video conferencing mode.
11. The selected candidate will certainly not have any type of right to claim for regular appointment in the council on the basis of contract appointment.
12. Applicants willing to apply for the post with a hard copy may download the application from the ICMR website. (www.main.icmr.nic.in). Duly filled application with Recent Photograph together with self-attested copies of all pertinent certifications as well as experience ought to be sent out to Room No 311, Division of ECD, Indian Council of.
    Medical Research, V. Ramalingaswami Bhawan, Ansari Nagar, New Delhi-110029 prior to the end of the last date as per advertisement.
13. Late received applications will not be taken into consideration. Only short-listed will certainly be informed by means of Phone/email as well as called for interview/video-conferencing, no correspondence will certainly be entertained in this regard.
14. Incomplete application, without a photo or without copies of pertinent certificates and also application not in prescribed format including Xcel sheet will certainly not be entertained. The Director ICMR reserves the right to increase/decrease the no. of posts or reject the applications or cancel the applications or cancel the notification without assigning any kind of reason thereof.
15. No TA/DA will be paid for appearing in interview/ video conferencing.
16. Any kind of canvassing by or on behalf of the applicants or to bring political or outside influence with regard to selection/recruitment will be a disqualification.
17. Shortlisted candidates will certainly be called for personal discussion and also/ or video conferencing after verification of essential qualification and also experience.
18. The Selection Committee reserves the right to reduce the experience in case of deserving applicants.

GENERAL CONDITIONS: The conditions of employment will be the same as that of the project staff on a contract basis. The candidates have no right to claim any kind of regular employment at this institute.

For any query please contact Mrs Harjeet Kaur Bajaj, Administrative Officer, Division of ECD or Mr Ramesh Chand, Section Officer, Division of ECD, ICMR HQ., New Delhi @ extension number 259 /284 or at 011-26589699.

For Post I

Salary: Rs. 57660/- monthly.

Essential Qualification: Candidates must possess 1st Class Master Degree in
Biotechnology or any equivalent post from a recognized university with 4 years of experience in the CRO industry/Pharma/Biotech/ Public Health/clinical research
OR
2
nd Class M. Sc. or second Class M. Pharm or any kind of equal post + PhD degree in relevant subjects from a recognized university with 4 years experience in experience in Pharma/Biotech/CRO industry/ Public Health/ clinical research.

Desirable Qualification and also & Experience:

1. A minimum of 2-year post-Doc experience in a biomedical subject particularly in
   health research related areas. Working experience in scholarly publications
2. Knowledge of computer applications or business intelligence tools/data management/ data synthesis/Report writing, data mining, writing popular articles/ working on databases.
3. Thorough knowledge of GCP, ICH guidelines as well as regulatory requirements for clinical trial conduct

Nature of duties:

1. To manage all clinical aspects of the study including assessing operational feasibility as well as recommending study execution plan; developing and handling comprehensive study timelines and metrics.
2. To participate in Selection as well as management/Oversight of CRO/vendors develops vendor specifications; review vendor reports, budgets and metrics.
3. To provide study-specific training as well as leadership to Clinical Research
   Staff, including CRO, CRAs, Sites and other contract personnel.
4. To plan, Execute and Lead study-specific meetings.
5. To participate in Site monitoring visits as well as oversee clinical monitoring activities ensuring compliance with Good Clinical Practices.
6. To prepare and/or review study-related Standard Operating procedures and also Documents.
7. To develop and also handle the study budget and also maintain it within financial
   goals.
8. To handle study files and process or administrative approvals.
9. Any other work assigned by the team leader pertaining to ITRC.
10. The job might require travel to the trial sites and also attending outstation meetings.

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For Post II

Salary: Rs. 57660/- monthly.

Essential Qualification: Applicants need to have a 1st Class Master Degree in Biochemistry/Biotechnology or 1st Class M.Pharm or any kind of equal post from a recognized university with 4 years experience in CRO industry/ Pharma/ Biotech/ Public Health/clinical research pertaining to clinical research/ trials.
OR.
2nd Class M. Sc. In Biochemistry/Biotechnology or 2nd Class M.Pharm or any kind of equivalent post + PhD degree in relevant subjects from a recognized university with 4 years experience in experience in Pharma/Biotech/CRO industry/ Public Health related to clinical research/ trials.

Desirable Qualification and also & Experience:

1. At the very least 2-year post-Doc experience in a biomedical subject particularly in.
   health research related areas. Working experience in Quality Control/Assurance.
2. Knowledge of computer applications or business intelligence tools/data management/ data synthesis/Report writing, data mining, writing popular articles/ working on databases.
3. Comprehensive knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial conduct.

Nature of duties:

1. To manage all clinical aspects of the study including assessing operational feasibility as well as recommending study execution plan; developing and handling comprehensive study timelines and metrics.
2. The job requires frequent All India travel to sites for monitoring, quality guarantee and also quality management for at the very least 15 days a month.
3. To prepare QA/QC Prepare for the sites for all studies and participate in Selection and management/Oversight of sites, CRO/vendors develops vendor specifications; review vendor reports, budgets and metrics.
4. To provide study-specific training as well as leadership to Clinical Research
   Staff, including CRO, CRAs, Sites and other contract personnel.
5. To plan, Execute and Lead study-specific meetings.
6. To participate in Site monitoring visits as well as oversee clinical monitoring activities ensuring compliance with Good Clinical Practices.
7. To prepare and/or review study-related Standard Operating procedures and also Documents.
8. To develop and also handle the study budget and also maintain it within financial
   goals.
9. To handle study files and process or administrative approvals.
10. Any other work assigned by the team leader pertaining to ITRC.
11. The job might require travel to the trial sites and also attending outstation meetings.

Click here for Application Format (Word Doc)

Click here for Application Format (Excel Sheet)

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