Freshers Walk-in for Pharmacovigilance on 8th & 9th Jan @ Mysore
PLEASE NOTE : BIOCLINICA IS CONDUCTING THIS WALK-IN INDEPENDENTLY AND NOT WITH PARTNERSHIP WITH CONSULTANCIES.
Bioclinica invites you for an opportunity to be part of our PHARMACOVIGILANCE team.
Meet us on 8th or 9th Jan 2019 between 9 AM to 1 PM at the below address:
Venue Details:
Bioclinica India Pvt Ltd
Silver Spirit Tech Park
317 (P), (PII) 318, Hebbal Industrial Area,
Mysore-16
JOB TITLE: DRUG SAFETY ASSOCIATE
WORK LOCATION: MYSORE
YEARS OF EXPERIENCE: 0 TO 2 YEARS
EDUCATION: M PHARMACY, PHARM D, BDS, MDS, MSc / BSc (Nursing)
ROLES & RESPONSIBILITIES
As Case Intake Member :
Silver Spirit Tech Park
317 (P), (PII) 318, Hebbal Industrial Area,
Mysore-16
JOB TITLE: DRUG SAFETY ASSOCIATE
WORK LOCATION: MYSORE
YEARS OF EXPERIENCE: 0 TO 2 YEARS
EDUCATION: M PHARMACY, PHARM D, BDS, MDS, MSc / BSc (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 to determine 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.
