Safety Data Associate

at  JAC Recruitment Singapore

COMPANY OVERVIEW

Our client, a global pharmaceutical company is now seeking a Safety Data Associate to be part of their Global Patient Safety (GPS) Data Management and will be responsible in performing safety data management of products in clinical trials and marketed drugs.

JOB REQUIREMENTS

Diploma or Degree with specialization in Pharmacy
Basic knowledge of Pharmacovigilance, pharmacology and the pharmaceutical industry is essential.
Working experience in drug adverse event reporting and ARISg/ARGUS database is an added advantage.
Proficient in working with IT systems and databases, well versed in MS Office applications.
Excellent interpersonal skills
Meticulous at work, eye for detail and self-motivated
Good team player, and at the same time able to work independently
Apply online or feel free to contact me directly for more information about this opportunity. Due to the high volume of applicants, we regret to inform that only shortlisted candidates will be notified. Thank you for your understanding.
EA JAC Recruitment Pte. Ltd.
EA Licence: 90C3026
EA Personnel: R1109147
EA Personnel Name: Noor Suliana Liza Binte Ab Lateb

Carry out drug adverse event case processing activities following our client’s policies and good Pharmacovigilance practice.
Review, verify process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency. Process cases based on these assessments.
Write and edit the case narrative.
Determine and perform appropriate case follow-up, including preparing follow-up requests.
Review processed cases to verify accuracy, consistency, and compliance with process requirements, and review case data for special scenarios.
Participate as appropriate in local internal and external drug safety activities.