Das ist der Job
Prepare clinical and regulatory documents needed for drug and device development.
Darum lohnt es sich
Arrange and conduct review meetings with the team and ensure delivery within project timelines. Eligible for long-term incentive programs and comprehensive benefits package. Coordinate review, approval, and quality control of other functions involved in document production.
Qualifications Minimum 4+ years in global pharma, biotech, or life science industry. Bachelor's degree required; scientific discipline preferred. Outstanding written and oral communication skills with knowledge of medical terminology. Additional Information Compensation range reflects base pay based on geographic location and job grade.
AbbVie is an equal opportunity employer committed to diversity and inclusion.
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