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Job Title: Global Director of Regulatory Affairs
Location: Illinois, Chicago
Discipline: Regulatory
Reference: CMMQ4126
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Description: global directorship/pharm & med device business
CMMQ4126
Global Director of Regulatory Affairs
Chicago, IL
-Provide strategic input into the development of assigned
projects within the Therapeutic Area.
-Responsible for handling complex issues and providing leadership where
appropriate to assigned development teams.
-Act as global regulatory lead on defined products
-Candidate will be responsible to define and implement a wide range of
global pharmaceutical regulatory strategies of new medicinal products
-Responsible for interaction with FDA, European Agencies as appropriate,
-Effectively use negotiation skills to resolve complex regulatory issues
in cross-functional teams to ensure meeting development objectives.
-Ability to effectively negotiate basic regulatory agreements with Global
Health Agencies.
-Responsible to manage and coordinate regulatory responses to agency
inquiries and maintain a high level of understanding of global regulatory
requirements
Qualifications: Minimum Requirements
-At least 12 years in Regulatory, R&D or related area with a minimum of 12
years direct Regulatory Affairs experience.
-International Travel Required
-Education Requirements BS, MS, PhD, or MD
-Percentage of Travel 20%
Apply to: Click Here
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