Neurology MedTech Regulatory VP - Strategy & Submissions
IQVIA
IQVIA MedTech hosts the MCRA team seeking a VP of Regulatory Affairs in Neurology MedTech to lead regulatory strategy and submissions for client companies. You will manage regulatory projects, mentor staff, and collaborate with multiple departments to advance therapies from concept through development and commercialization. Experience in neurology medical devices and 15+ years in regulatory affairs are required. #J-18808-Ljbffr IQVIA
$169.2k
MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech... ...commercialization, offering expertise in regulatory strategy, clinical trial design and execution,... ...supporting regulatory strategy and submissions for the firm’s clientele, and managing...RegulatoryFull timePart timeWork experience placementImmediate startWorldwide$225k - $300k
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