Pharmacovigilance Associate II
VirtualVocationsFontana, California, United Statesjob_description.job_card.variable_days_ago
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A company is looking for an Associate II, Pharmacovigilance.
Key Responsibilities
Author Safety Management Plan for assigned studies
Review incoming SAE data for completeness and accuracy
Generate regulatory reports and perform safety submissions as needed
Required Qualifications, Training, and Education
Bachelor's degree in a science-related field, nursing, or equivalent
Minimum of 1 year of pharmacovigilance experience (pre-approval clinical trials)
Computer literacy and strong working knowledge of MS Office applications
Ability to work independently and prioritize effectively
Strong understanding of medical and scientific terminology and international regulations
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Associate Ii • Fontana, California, United States
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