Adverse Event Review Specialist
hace 3 semanas
We are seeking an experienced Adverse Event Review Specialist to join our team at Pfizer. As a key member of our pharmacovigilance department, you will play a crucial role in ensuring the safety profile of our products and meeting regulatory requirements.
Key Responsibilities:- Report Review and Processing: You will be responsible for reviewing and processing reports of adverse drug experiences, identifying and prioritizing cases, assessing complexities, and documenting case narratives.
- Regulatory Compliance: Your tasks will include generating reports that adhere to regulatory compliance timelines, liaising with stakeholders, including Pfizer Country Organizations and Clinical Development, and developing expertise on Pfizer's products and regulations.
- Bachelor's Degree: A Bachelor's degree in a science-related field, pharmacy, or nursing is required. Healthcare professional qualification is preferred.
- Communication Skills: Excellent communication and computer literacy skills are essential for this role.
- Language Fluency: Fluency in spoken and written English is mandatory.
$70,000 - $100,000 per year, depending on experience.
Work Location:This position is located on premise.
About Pfizer:Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation.
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