Safety Data Governance Specialist

hace 2 semanas


San José, San José, Costa Rica Pfizer A tiempo completo
About the Role

Pfizer is seeking a skilled Safety Data Management Specialist to join our team

The ideal candidate will be responsible for monitoring our drug, biologics, and medical devices surveillance program, including intake, evaluation, and processing of adverse reports. This role will also support clinical trials and post-marketing activities.

In this position, you will contribute to the completion of complex projects, manage your time to meet agreed targets, and develop plans for work activities on your own projects within a team. You will also provide oversight, team mentoring, and review and analyze safety-related reports.

Key qualifications for this role include a Bachelor's Degree in Health Sciences, 3+ years of experience, and solid knowledge of global regulations and guidelines for drug development.



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