Fresher's Walk-in for Pharmacovigilance on Sunday, 29th July @ Bioclinica, Bangalore, for Exp. 0 - 2 yrs.

Bioclinica invites you for an opportunity to be part of our PHARMACOVIGILANCE team!


**Candidates who are attending this drive should be registered or applied for the state council registration


Meet us on SUNDAY, 29th July between 9 AM to 1 PM at the below address:

Bioclinica India Pvt Ltd
No:18/2 & 18/3, V G Heritage,
Vanivilas Road, Kanakapura,
Basavanagudi, Bengaluru,
Karnataka 560004


JOB TITLE: DRUG SAFETY ASSOCIATE

WORK LOCATION: MYSORE

YEARS OF EXPERIENCE: 0 TO 2 YEARS

EDUCATION: B PHARMACY, M PHARMACY, PHARM D, BDS, MDS, BAMS, BHMS, BSC NURSING, MSC 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.