Job Type : Walk-In Interview
Job Title: Drug Safety Associate
Work Location: Mysore
Years Of Experience: 0 to 2 Years
Educational Qualification: B Pharmacy, M Pharmacy, Pharm D, BDS, MDS, BAMS, BHMS, B.Sc Nursing, M.Sc Nursing
ROLES & RESPONSIBILITIES
As Case Intake Member:
– Responsible for case intake, duplicate check, and registration
– Maintain log of source documents and other communications
As Case Processor:
– Responsible for data entry of individual case safety reports into the safety database.
– Review and evaluate AE case information to determine required action based on and following internal policies and procedures
– Process all incoming cases in order to meet timelines
– Full data entry including medical coding and safety narrative
As Medical Coder
– Responsible for coding all medical history, events, drugs /procedures/indications and laboratory tests according to the appropriate dictionary (For e.g. MedDRA, Company Product Dictionary, WHO-DD)
As Narrative Writer
– Responsible for writing medically relevant safety narrative of cases and checking the completeness and accuracy of the data entered in the various fields.
As Literature Review Specialist
– Ensure effective and accurate collection, recording, review and reporting of literature searches conducted.
– Review of literature articles to identify case safety reports.
– Responsible for operational Pharmacovigilance activities for assigned developmental and /or marketed products.
– Assist in signal generation and safety analysis activities.
– Ensure quality of literature searches and reporting.
– Review of local/global literature reports determining regional reportability.
– Create/maintain study summary documents.
– Assist with narrative writing for periodic/ad hoc submissions.
– Assist with ad hoc or routine safety monitoring activities
– Responsible for case intake, duplicate check, and registration
– Maintain log of source documents and other communications
As Case Processor:
– Responsible for data entry of individual case safety reports into the safety database.
– Review and evaluate AE case information to determine required action based on and following internal policies and procedures
– Process all incoming cases in order to meet timelines
– Full data entry including medical coding and safety narrative
As Medical Coder
– Responsible for coding all medical history, events, drugs /procedures/indications and laboratory tests according to the appropriate dictionary (For e.g. MedDRA, Company Product Dictionary, WHO-DD)
As Narrative Writer
– Responsible for writing medically relevant safety narrative of cases and checking the completeness and accuracy of the data entered in the various fields.
As Literature Review Specialist
– Ensure effective and accurate collection, recording, review and reporting of literature searches conducted.
– Review of literature articles to identify case safety reports.
– Responsible for operational Pharmacovigilance activities for assigned developmental and /or marketed products.
– Assist in signal generation and safety analysis activities.
– Ensure quality of literature searches and reporting.
– Review of local/global literature reports determining regional reportability.
– Create/maintain study summary documents.
– Assist with narrative writing for periodic/ad hoc submissions.
– Assist with ad hoc or routine safety monitoring activities
Venue :
Bioclinica India Pvt. Ltd
No:18/2 & 18/3, V G Heritage,
No:18/2 & 18/3, V G Heritage,
Vanivilas Road, Kanakapura,
Basavanagudi, Bengaluru,
Karnataka 560004
Candidates who are attending this drive should be registered or applied for the state council registration
Meet us on
Meet us on
Date : Saturday, 18th August 2018
Time :between 9 AM to 1 PM at the below
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