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Safety Data Management Expert
hace 2 semanas
About the Role
We are seeking a highly skilled Safety Data Management Specialist to join our team at Pfizer.
The ideal candidate will have experience in pharmacovigilance, regulatory compliance, and data management. They will be responsible for monitoring drug surveillance programs, processing adverse reports, and supporting clinical trials and post-marketing activities.
Key Responsibilities:
- Monitor and manage safety resources in the local team.
- Review and analyze safety-related reports to determine the safety profile of Pfizer's products.
- Manage project and process management meeting established deadlines.
Requirements:
- Bachelor's Degree in Health Science or related field.
- 3+ years' experience in pharmacovigilance, regulatory compliance, or related field.
- Demonstrated organizational/project management skills.
- Solid knowledge of global regulations and guidelines for drug development.
About Us
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
