ICMR jobs for Project Scientist Support-II Clinical Services in Delhi. Last Date to apply: 25 Mar 2021
Project Scientist Support-II Clinical Services
ICMR
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-II (Clinical Services)
No. of Vacancy: Two
Essential Qualification & Minimum Experience required: 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 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 an 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.
v. Thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial conduct. vi. Good communication skills
Consolidated Emoluments: Rs. 72325/-
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:
a. Monitor the clinical trial and Prepare strategy for site monitoring and timely completion of recruitment targets and follow -up visits
b. Checking of resources and Site initiation
c. Monitor vaccine trial, check all the source documents and completeness of data CRFs and ensuring timely completion of data entry in compliance with study protocol.
d. Review SAE tracker and SAE document repository every 15 days
e. Prepare a patient tracker and discuss with site PI to ensure compliance and minimize missing visits of subjects
f. To match the tracker every week against recruitment target for each site and take necessary actions accordingly
g. Discussion with PI’s and project staff for patient compliance
h. Review of Ensure that all processes contributing to the performance of a clinical trial are conducted properly.
i. Prepare and assist in preparing annual reports and quality trending reports.
j. Prepare the site wise and consolidated site report regarding enrollment data vs. targets and share with Team lead/PO every week.
k. Keep upto date with all quality and compliance issues and Report the status of the quality levels of the staff, systems and production activities.
l. Any other job assigned by the PI or Programme officer
m. Job requires frequent All India travel to sites for monitoring, quality assurance and quality management for at least 15 days a month.
Age Limit: 40 years. (Relaxable to OBC and SC/ST Candidate as per Govt. of India)
Job Particulars
Role research jrf srf
Education MD, MBBS, MS, PG Diploma
Who can apply Experienced (1 to 3+ Years)
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id1146285
Job Category Govt Jobs , Research , 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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