Safety Data Management Specialist

hace 2 meses


San José, San José, Costa Rica Pfizer A tiempo completo
Purpose:

You will be responsible for monitoring and evaluating adverse reports received by the company. This includes intake, evaluation, and processing of these reports to ensure the safety profile of Pfizer's products is determined in accordance with regulatory requirements.

Key Responsibilities:
- Monitor and evaluate adverse reports
- Process and analyze data to determine the safety profile of Pfizer's products
- Collaborate with cross-functional teams to achieve business objectives
- Develop and maintain advanced knowledge of Pfizer's products and regulatory guidelines

Requirements:
- Bachelor's Degree
- 3+ years of experience in pharmaceutical safety
- Strong analytical and problem-solving skills
- Excellent communication and collaboration skills
- Fluency in English

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