Writes CERs, SSCPs, SOAs, and LRRs.
Participates in literature reviews: search, screen, extract data, analyze.
Summarizes data for medical devices and performs risk/benefit analysis.
Compares safety and performance to state-of-the-art and investigates outcomes.
Uses MS Office, EndNote, Distiller, Wrike, and in-house AI tools.
Follows procedures and regulatory requirements; partners with cross-functional teams.

🎯 Requirements

Bachelor of science or equivalent in health-related or scientific field.
1-2 years CER writing experience.
Experience with medical devices preferred.
Strong writing and data synthesis skills.

🎁 Benefits

Flexible Working Hours
Team events and end of year party
Employee satisfaction survey
Health Insurance

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