
Safety Data Management Specialist
- Escazú, San José
- Permanente
- Tiempo completo
- Monitor and manage the company's drug, biologics, and medical devices surveillance program, ensuring comprehensive oversight.
- Intake, evaluate, and process adverse reports for both clinical trials and post-marketing activities, ensuring accurate and timely handling.
- Act as a subject matter expert, liaising with key partners regarding safety data collection, reconciliation, and ensuring regulatory compliance.
- Review, analyze, prepare, and complete safety-related reports to determine the safety profile of products and meet regulatory requirements.
- Verify the accuracy, consistency, and compliance of processed cases, and review case data for special scenarios, ensuring high standards are maintained.
- Manage safety resources within the local team, provide specific pharmacovigilance or product knowledge, mentor colleagues, and maintain advanced knowledge of Pfizer's product portfolio and corporate policies.
- BA/BS with at least 2 years of experience or MBA/MS with any years of experience
- Strong organizational and project management skills
- Solid knowledge of global regulations and guidelines for drug development
- Demonstrated analytical and statistical skills
- Fluency in spoken and written English
- Master's degree
- Relevant pharmaceutical industry experience
- Familiarity with management of performance metrics
- Strong problem-solving skills
- Proficiency in safety database and data mart search functions