Global Safety Senior Manager with Direct Pharmacovigilance Experience (Fully Remote Job)
Location: Thousand Oaks, CA
Terms: Contract W2
Duration : 12 Months Contract
Skill Sets:
Direct Pharmacovigilance experience (Not PV operation or safety reporting)
Safety signal assessment and management experience
Aggregate data review and assessment
Must-Have Experience (all three ideal):
• Safety signal management
• Aggregate data review and assessment
• Pharmacovigilance signal-related activities (not operations)
Day to Day Responsibilities:
Review daily SAEs
Assist GSO and other scientist is filing activities, responds to RTQs, daily routine PV activities, and other ad hoc requests
Description:
The Global PV Sr. Scientist works with the Therapeutic Safety Teams for safety assessment activities for medical/scientific operations.
This person will also provide scientific and compliance expertise as needed to GPS.
Serious Adverse Events (SAEs) in Pharmacovigilance is a critical Safety Process, particularly during clinical trials
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