The Director will partner with all Regulatory Affairs functions, Medical Affairs, Legal, Compliance, Commercial and International distributors and will serve as a key member of the Medical/Legal/Regulatory (MLR) Review Committee. • Conduct review and approval of advertising/promotional materials as the lead regulatory reviewer on the MLR Committee for US and international markets. • Serve as an expert resource for regulatory advertising/promotion advice across departments. • A minimum of 10 years of biopharmaceutical industry experience, with a minimum of 8 years of experience in the regulatory review of advertising/promotional materials for prescription drug and/or biologic products. Or, feel free to email your resume
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