Highly motivated and detail-oriented Adverse Event Case Intake Processor to join our growing Pharmacovigilance team. In this critical role, you will be responsible for the accurate and timely intake, processing, and tracking of adverse event reports received from various sources. You will play a vital role in ensuring the safety of our products by diligently adhering to regulatory guidelines, internal Standard Operating Procedures (SOPs), and global best practices.

COUNTRY-SPECIFIC REQUIREMENTS:

• Adhere to specific country requirements for case intake and processing, Adhere to specific requirements as outlined in the provided documentation.
• AMERS, EMEA and APAC Countries PII privacy requirements, TGA Health Authority report reception and processing.
• Special handling for fatal cases; SAE reporting requirements for I-SEA countries.

QUALIFICATIONS

Education: Bachelor’s degree in a life science field (e.g., Biology, Pharmacy, Nursing) or equivalent experience.
Fluent local language skills & excellent command of the English language
Experience: 1+ years of experience in pharmacovigilance or a related field (e.g., clinical research, medical information) preferred.

SKILLS:

• Strong attention to detail and accuracy.
• Excellent organizational and time-management skills.
• Proficiency in data entry and management.
• Strong written and verbal communication skills.
• Ability to work independently and as part of a team.
• Proficiency in English language; fluency in other languages (e.g., Spanish, French, German) is a plus.
• Knowledge of medical terminology and pharmacovigilance regulations is preferred.
• Technical Skills:
• Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
• Experience with safety databases (e.g., Argus, APEX) is a plus.