Safety Data Associate

• 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.

• 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