The Adverse Event Intake Coordinator plays a critical role in ensuring the timely and accurate processing of adverse event reports related to our company’s products. This position is responsible for receiving, reviewing, and processing incoming adverse event reports (AEs) from various sources, including healthcare professionals, consumers, and regulatory agencies. The ideal candidate is highly organized, detail-oriented, and possesses strong communication and problem-solving skills.

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 year of experience in pharmacovigilance or a related field preferred.

SKILLS:

• Strong attention to detail and accuracy
• Excellent organizational and time-management skills
• Proficiency in Microsoft Office Suite (Word, Excel, Outlook)
• Strong written and verbal communication skills
• Ability to work independently and as part of a team
• Excellent problem-solving and analytical skills

PREFERRED QUALIFICATIONS:

• Experience with electronic data capture (EDC) systems
• Knowledge of medical terminology and coding systems (e.g., MedDRA)
• Experience with regulatory submissions