BIOCLINICA - Freshers Walk-In for Pharmacovigilance on 8th & 9th Jan' 2019 @ Mysore

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 : 

·         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.