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Job Requirements
Education and experience
University degree - medical or paramedical (pharmacy,
biology, veterinary etc.), or equivalent by experience
Breadth of regulatory experience in drug development
and commercialization (e.g. experience in multiple products, multiple
phases of development, multiple therapeutic areas)
Experience with EU regulatory procedures (CP, MRP,
national)
Experience in working in project teams and/or a matrix
organization
Skills
Negotiating and conflict handling skills
People management skills
Complex project management skills
Oral & written communication skills
Organization & multi-tasking skills
Knowledge
Excellent knowledge of English
Knowledge of the applicable therapeutic area
In depth knowledge of the regulatory environment,
guidelines and practice of EMEA regions
My Profile
Create and manage profiles for future opportunities.