Medical Doctor or equivalent degree required
Board certification(s) are preferred
Specialty education(e.g. residency/fellowship) required in neurology
This should be accompanied by patient treatment and/or research experience
1-3 years of industry experience required
Experience should be in clinical development in a Pharmaceutical, Biotech or CRO organization
Excellent English, both written and spoken is a must
Ability to travel
Shown understanding with NDA submission process
Shown understanding of regulatory guidelines for adverse event reporting
Proven interpersonal skills enabling to lead a study team, while recognizing individual expert competencies, providing medical advice and evaluations exercising judgment in which issues need to be escalated immediately
Pro-active problem solver with negotiation skills, remaining sensitive to the different cultural needs in a global organization
Strong communication skills to ensure close collaboration with the cross functional team members so that study plans and status are transparent, and that risks, issues, and results are clear to all involved parties