Safety Data Analyst
Há 1 mês
As a leading contract research organization (CRO), Fortrea is dedicated to delivering high-quality clinical development solutions across various therapeutic areas. We are seeking a highly skilled Safety Data Analyst to join our team.
The successful candidate will be responsible for managing the receipt and processing of adverse event reports, ensuring timely and accurate data entry, and maintaining a comprehensive understanding of Standard Operating Procedures (SOPs) and guidance documents. Key responsibilities include:
- Data entry of safety data onto adverse event databases and tracking systems
- Review of adverse events for completeness, accuracy, and appropriateness for expedited reporting
- Code adverse events accurately using MedDRA and determine listedness against applicable labels
- Identify clinically significant information missing from reports and ensure its collection, preparing follow-up correspondence as needed
The ideal candidate will possess excellent analytical and problem-solving skills, with the ability to work effectively in a team environment. A strong understanding of pharmacovigilance and safety management principles is essential. If you are a detail-oriented and organized individual with a passion for delivering high-quality results, we encourage you to apply.
Fortrea is proud to be an Equal Opportunity Employer, committed to fostering a diverse and inclusive work environment. We do not discriminate based on race, religion, color, national origin, gender, family or parental status, marital status, sexual orientation, gender identity, age, veteran status, disability, or any other protected characteristic.
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