Join Alexion as a Pharmacovigilance Quality Specialist on a 12-month contract and contribute to life-saving medicines. Drive patient safety efforts by analyzing adverse event data.
This role is pivotal to the Patient Services Team for all US approved products. You will manage case processing, ensure quality compliance, and respond to adverse event inquiries. Your analytical skills will help identify trends, supporting the mission of Alexion in enhancing patient care.
Key Responsibilities:
Support pharmacovigilance activities within Patient Services
Collect and report data on adverse events and safety info
Work with teams to confirm accurate safety data
Participate in pharmacovigilance training sessions
Conduct quality reviews for submissions of adverse events
Requirements:
1+ years in pharmaceutical or biotech industry
Solid communication and attention to detail
Adaptive problem solver and decision maker
Ability to manage multiple tasks independently
Familiarity with Windows-based software and Salesforce
Utilize your passion for patient-centric strategies in promoting safety within Alexion's unique workplace.
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