Safety Data Coordinator

We are seeking a Safety Data Coordinator to review, assess, and process safety data and information across service lines. The successful candidate will distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members.

Main Responsibilities:

• Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
• Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities.
• Ensure compliance with quality, productivity, and delivery standards per project requirements.
• Liaise with different functional team members and healthcare professionals to address project-related issues.

Qualifications:

• Bachelor’s degree in Life sciences or a related field.
• Fluency in English and Spanish.
• 1 or 2 years of pharmacovigilance experience.
• Experience with Safety Databases, such as ARGUS.

Work Modality:

• 100% home-based