Pharmaceutical Safety Specialist for Regulatory Compliance
hace 16 horas
Pfizer Worldwide Medical and Safety colleagues play a crucial role in connecting evidence-based medical decision support with colleagues and stakeholders to enable better health and treatment outcomes.
We empower healthcare decisions regarding the safe and appropriate use of medicines for patients by monitoring our drug, biologics, and medical devices surveillance program.
This includes intake, evaluation, and processing of adverse reports received, supporting clinical trials as well as post-marketing activities.
As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team.
Your focus and ability to meet team targets will help in completing important deliverables on time.
You will be responsible for managing safety resources in the local team, providing specific pharmacovigilance or product knowledge and experience, and mentoring colleagues accordingly.
A key responsibility will be to develop and maintain advanced knowledge of all products within the Pfizer portfolio.
You will also design and oversee the tracking of applicable safety metrics and manage project and process management meeting established deadlines.
To succeed in this role, you must have a Bachelor's Degree, 3+ years' experience, and demonstrated organizational/project management skills.
You should have solid knowledge of global regulations and guidelines for drug development, demonstrated analytical and statistical skill, and ability to make decisions independently and resolve issues appropriately.
Fluent in spoken and written English is essential, and a Master's degree, relevant pharmaceutical industry experience, and familiarity with management of performance metrics are desirable.
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