
Senior Pharmacovigilance Lead — Safety Data & Submissions
Worldwide Clinical Trials, Milwaukee, WI, United States
A global clinical research organization is seeking a Senior Drug Safety professional in Milwaukee, WI. This role involves managing the collection and reporting of Serious Adverse Event data, leading studies, and mentoring junior staff. Candidates should have a Bachelor's degree in a science-related field and at least 5 years of pharmacovigilance experience in clinical trials. A commitment to inclusivity and collaboration is a core value within the organization.
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