ICMR jobs for Project Scientist Support-V Clinical Coordinator/QC in Delhi. Last Date to apply: 25 Mar 2021
Project Scientist Support-V Clinical Coordinator/QC
ICMR
Expired
Posted: 15 Mar 21
Job Description
Indian Council of Medical Research (ICMR) invites application for the position Project Scientist Support-V (Clinical Coordinator/QC)
No. of Vacancy: One
Essential Qualification & Minimum Experience required: Candidates should possess 1st Class Master Degree in Biochemistry/Chemistry/Pharmacology/Biotechnology or 1st Class M. Pharm or any equivalent post from a recognized university with 4 years’ experience in CRO industry/Pharma/Biotech/ Public Health/clinical research related to clinical research /trials OR 2 nd Class M. Sc. In Biochemistry/Chemistry/Pharmacology/Biotechnologyor 2nd Class M. Pharm or any 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:
a. At least 2 year post Doc experience in biomedical subject particularly in health research related areas. Working experience in Quality Control/Assurance
b. Knowledge of computer applications or business intelligence tools/data management/data synthesis/Report writing, data mining, writing popular articles/working ondatabases.
c. Thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical trialconduct
Consolidated Emoluments: Rs. 57660/- per month
Tenure: Upto 31st March 2022. May continue for another year based on performance evaluation report.
Project: India TB Research Consortium – Project Management Unit
Nature of duties:
i. To manage all clinical aspects of study including assessing operational feasibility and recommending study execution plan; developing and managing comprehensive study timelines andmetrics
ii. Job requires frequent All India travel to sites for monitoring, quality assurance and quality management for at least 15 days a month.
iii. To prepare QA/QC Plan for the sites for all studies and participate in Selection and management/Oversight of sites, CRO/vendors, develops vendor specifications; review vendor reports, budgets andmetrics
iv. To provide study specific training and leadership to Clinical Research Staff, including CRO, CRAs, Sites and other contractpersonnel
v. To plan, Execute and Lead study specificmeetings
vi. To participate in Site monitoring visits and oversee clinical monitoring activities ensuring compliance with Good ClinicalPractices
vii. To prepare and/or review study related Standard Operating procedures and Documents
viii. To develop and manage study budget and maintain it within financialgoals
ix. To manage study files and process or administrativeapprovals
x. Any other work assigned by the team leader pertaining toITRC
xi. The job may require travel to the trial sites and attending outstationmeetings
Age Limit: 40 years. (Relaxable to OBC and SC/ST Candidate as per Govt. of India)
Job Particulars
Role research jrf srf
Education M Phil / Ph.D, M.Pharm, ME/M.Tech, MSc
Who can apply Experienced (3 to 3+ Years)
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id1146249
Job Category Govt Jobs , 1 to 3 Yr Exp
Locality Address
State Delhi
Country India
About Company
The Indian Council of Medical Research (ICMR), New Delhi, the apex body in India for the formulation, coordination and promotion of biomedical research, is one of the oldest medical research bodies in the world.
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