Associate Director, Medical Compliance Operations - Material Review
AbbVie
About this role
The Associate Director of Global Material Review Compliance at AbbVie is responsible for implementing processes and standards to ensure compliance in the review and development of medical content for pharmaceutical promotional and non-promotional materials. They support adherence to regulatory standards, provide training, and collaborate with various global teams to maintain high quality and compliant scientific communication.
Skills
About AbbVie
abbvie.caAbbVie is a global biopharmaceutical company (spun out of Abbott in 2013) that discovers, develops and commercializes specialty medicines across immunology, oncology, neuroscience, eye care and virology. It is best known for blockbuster brands such as Humira and a growing portfolio that includes targeted biologics and small molecules (and expanded capabilities after the Allergan acquisition). AbbVie emphasizes large-scale R&D, clinical development and strategic partnerships to advance its pipeline and bring therapies to patients worldwide. Headquartered in North Chicago, Illinois, the company operates globally with a focus on long-term innovation and patient outcomes.
About AbbVie
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Leadership Team
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
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and employee contacts for AbbVie.
Salary
$135k – $170k
per year
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