ICMR Jobs 2019: 09 Consultant Vacancy for MS/MD, DNB, MBBS, M.Pharma, M.Sc, M.Phil/Ph.D, BAMS Salary 70,000 published on 17th June 2019

On 14/06/2019, ICMR announced Job notification to hire candidates who completed MS/MD, DNB, MBBS, M.Pharma, M.Sc, M.Phil/Ph.D, BAMS for the position of Consultant.
Vacancy 1 Consultant
Qualification MS/MD, DNB, MBBS, M.Pharma, M.Sc, M.Phil/Ph.D, BAMS
Vacancies 09 Posts
Salary Rs. 70,000/-Per Month
Experience 1 - 10 years
Job Location New Delhi
Walk-In Date 24/06/2019
Other Qualification Details:

1. Post Consultant Clinical Operations

a. Qualification: Post Graduate Degree (MD)/MS/DNB) after MBBS with one year of demonstrated experience in clinical research/trial from reputed institutions. OR MBBS or equivalent with four year of demonstrated experience in clinical research /trial from reputed Institutions. OR I stclass Masters in M.Pharma or M.Sc in Pharmacology/Medical Microbiology/ Biochemistry/BiotechnoIogy/ Clinical Research with 4years of demonstrated experience of clinical research/trial OR 2 n class Masters in M.Pharma , M.Sc in Pharmacology/Medical Microbiology/ Biochemistry/BiotechnoIogy/ Clinical Research with ars ost Ph.D demonstrated experience of clinical

b. Desirable: Experience in implementing / conducting and all aspects of regulatory Vaccine/drug trial/clinical research. Experience in establishing clinical trial sites, management & implementation of trials and managing and maintaining databases for qualitysystems. Able to write& review SOPs and logs relevant requirementrial sites. Able to prepare project management plan, study monitoring plan for regulatory clinical trials Thorough knowledge of Schedule Y, new clinical trial guidelines. GCP, GCLP, ICII guidelines andregulatory requirements and new clinical trial rules for conduct of clinical trial.

2. Consuliant (Scientific) Biomedical Research: 

a. Qualification: Post Graduate Degree (MD)/MS/DNB) after MBBS with one year of demonstrated experience in clinical research/trial from reputed institutions. OR MBBS or equivalent with four year of demonstrated experience in clinical research /trial from reputed Institutions. OR I stclass Masters in M.Pharma or M.Sc in Pharmacology/Medical Microbiology/ Biochemistry/BiotechnoIogy/ Clinical Research with 4years of demonstrated experience of clinical research/trial OR 2 n class Masters in M.Pharma , M.Sc in Pharmacology/Medical Microbiology/ Biochemistry/BiotechnoIogy/ Clinical Research with ars ost Ph.D demonstrated experience of clinical

b. Desirable: Experience conducting multicentric Experience in research//Biomedical Research. Experience in managing and maintaining databases for quality systems. Able to prepare SOPS, project management plan and study monitoring plan for trial conduct. Thorough knowledge of GCP, GCLP, ICII guidelines and regulatory requirements for clinical trial. Good communication skills

3. Consultant (Scientific) Clinical Coordinator

a. Qualification: Post Graduate Degree (MD/MS/DNB/Ph.D) after MBBS with one year of demonstrated experience in clinical research/Biomedical Research from reputed Institutions. OR MBBS or equivalent with four year ofclinical experience in Government Institutionof which 2 years should be demonstrated experience in clinical research/BiomedicaI Research from reputed Institution. OR I stclass Masters in M.Pharma , M.Sc in Pharmacology/Mcdical Microbiology / Biochemistry/ Biotechnology with 4 yearsof demonstrated experience in clinical research/ /Biomedical Research from reputed Institution. OR 2n class Masters in M.Pharma , M.Sc in Pharmacology/Medical Microbiology/ Biochemistry/Biotechnology/ Clinical Research with Ph.D in an of the above disci lines with 2 years post Ph.d)

b. Desirable: Experience in conducting Vaccine/drug trial/clinical research//BiomedicaI Research. Experience in managing and maintaining databases for quality systems. Knowledge of preparation of the protocol and budget for studies. Update the landscape documents in all thematic areas of TB Able to prepare SOPs for trial conduct. Thorough knowledge of GCP, ICH guidelines and regulatory requirements för clinical trial conduct. Good communication skills

4. Consultant (Scientific) Clinical Development

a. Qualification: Post Graduate Degree (MD/MS/DNB/Ph.D) after MBBS with one year of demonstrated experience in clinical research/Biomedical Research from reputed Institutions. OR MMBBS or equivalent with four year of clinical experience Government Institution of which 2 years should be demonstrated experience in clinical research /Biomedical Research from reputed Institution. OR I stclass Masters in M.Pharma , M.Sc in Pharmacology/Medical Microbiology / Biotechnology with 4 years of demonstrated experience in clinical research/ Biochemistry /Biomedical Research from reputed Institution. OR 2ndclass Masters in M.Pharma , M.Sc in Pharmacology/Medical Microbiology/ Biochemistry/BiotcchnoIogy/ Clinical Research with Ph.l) in any of the above disciplines with 2 years post Ph.D demonstrated experience of clinical research/trial.

b. Desirable: Experience in conducting clinical researchBiomedical Research. Experience in managing and maintaining databases for quality systems. Have medical writing skills for writing protocols/ clinical study reports/ prepare CRFs, proforma etc. Able to prepare SOPs for clinical trial conduct. Thorough knowledge of GCP, GCLP, ICH guidelines and regulatory requirements for clinical trial. Good communication skills

5. Consultant (Senior Project Manager)

a. Qualification: Post Graduate Degree (MS/MD/ DNB)NB/Ph.d) after MBBS with Four years 01 dernonstrated core experience after post graduation in Vaccine/drug trial from reputed Institution/CR. OR MBBS or equivalent with 8years of demonstrated core experience in managing regulatory Vaccine/drug trial/ from reputed Instilution/CR(). OR I stclass Masters degree M.Pharma/ or M.Sc in Pharmacology/ Biotechnology/liIO sciences with 8 years of demonstrated core experience in managing / monitoring regulatory Vaccine/drug trial from reputed Institution

b. Desirable: Experience in conducting Vaccine/drug trial/clinical research. Fxperience in establishing clinical trial sites, management & implementation of trials and managing and maintaining databases for quality systems. Able to prepare & review SOPs and logs relevant requirement for trial sites 'lhorough knowledge of new clinical trial rules, Schedule Y, GCP, (GCLP, ICII guidelines and regulatory requirements for conduct of clinical trial. Good communication skill

Consultant (Scientific) Clinical Service: 

a. Qualification: Post Graduate Degree (MD/MS/DNB/Ph.D) after MBBS with one year Of demonstrated experience in Vaccine/drug trial/clinical research/Clinical management from reputed Institutions. OR MBBS or equivalent with four year of clinical experience in Government Institution or which 2 years should be demonstrated experience in regulatory Vaccine/drug trial/clinical research from reputed Institutions.

b. Desirable: Experience in conducting Vaccine/drug trial/clinical research/CIinicaI Management. Able to prepare safety reports and ensure the timely management and reporting of AES an SAEs by sites by supporting them Experience in managing and maintaining databases for qualitysystems. Able to prepare SOPs for trialconduct and write safety reports and SAE narratives. Thorough knowledge of GCP, ICH guidelines andregulatory requirements for clinical trialconduct. communication skills

Consultant (Project Manager): 

a. Qualification: MBBS/BAMS or equivalent with 4year of demonstrated core clinical experience of managing/monitoring of regulatory clinical trials specially Vaccine/drug trial/clinical research from reputed Institutions. OR 1st Class Masters M.Pharma or M.Sc in Life sciences with4 years of core experience in managing/monitoring of regulatory clinical trials specially Vaccine/drug trial from reputed Institutions OR 2ndclass Masters in M.Pharma/M.Sc in life sciences with Ph.D and 3 years of post Ph.D demonstrated core experience in managing/monitoring of regulatory clinical trials speciallyVaccine/drug trial from reputed Institutions.

b. Desirable: Experience in conducting/managing and monitoringregulatory clinical research/ trials and carry out all the activities related to regulatory trials Experience in checking all source documents and cross check data entry in CRFs. Experience in managing and maintaining databases for quality systems. Able to prepare SOPS, logs etc. for trial conduct. Thorough knowledge of New clinical trial guidelines, Schedule Y, GCP, GCLP, ICH guidelines and regulatory requirements for clinical trial conduct. Good communication skills

Tenure: One Years

Age: Upto 70 years

Venue

Indian Council of Medical Research, V. Ramalingaswami Bhawan, Ansari Nagar, New Delhi, Delhi 110029

Selection Procedure

1. Written
2. Interview

How to Apply

The Walk In Interview will be held on 24/06/2019.The candidates should bring 5 copies of Biodata along with all original certificates of educational qualifications (from SSC onwards), experience, Aadhaar Card, with two set of photocopies of the supportive documents duly attested (can be self-attested) along with a passport size photograph for attending the Written Test/ interview.
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