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ICMR jobs for Project Scientist Support-V in Delhi. Last Date to apply: 25 Mar 2021

Project Scientist Support-V

ICMR
experience-icon 3 to 3+ Years
salary-icon Not disclosed
Expired

Posted: 15 Mar 21

Job Description

Advertisement No. 1/2021

Indian Council of Medical Research (ICMR) invites application for the position Project Scientist Support-V (Clinical Operations)

No. of Vacancy: One

Essential Qualification & Minimum Experience required: Candidates should possess 1st Class Master Degree in Biotechnology/clinical Pharmacology 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 OR 2 nd Class M. Sc. or 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/ clinical research

Desirable: 
i. At least 2 year post Doc experience in biomedical subject particularly in health research related areas. Working experience in scholarly publications
ii. Knowledge of computer applications or business intelligence tools/data management/data synthesis/Report writing, data mining, writing popular articles/working on databases.
iii. Thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial conduct

Consolidated Emoluments: Rs. 57660/- per month

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

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 and metrics
ii. To participate in Selection and management/Oversight of CRO/vendors, develops vendor specifications; review vendor reports, budgets and metrics
iii. To provide study specific training and leadership to Clinical Research Staff, including CRO, CRAs, Sites and other contract personnel iv. To plan, Execute and Lead study specific meetings
v. To participate in Site monitoring visits and oversee clinical monitoring activities ensuring compliance with Good Clinical Practices
vi. To prepare and/or review study related Standard Operating procedures and Documents
vii. To develop and manage study budget and maintain it within financial goals
viii. To manage study files and process or administrative approvals
ix. Any other work assigned by the team leader pertaining to ITRC
x. The job may require travel to the trial sites and attending outstation meetings

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

Job Particulars

Who can apply Experienced (3 to 3+ Years)
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id1146248
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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