DIRECTOR OF REGULATORY AFFAIRS CAROT CTR
Duties: The Director of Regulatory affairs will be responsible for working closely with the FDA representing the CAROT on all continuing and upcoming trials. The Director is responsible for developing and implementing innovative regulatory strategies in support of our on-going ocular clinical trials. In addition, the Director may represent the center with contractors and corporate partners, and serve as the regulatory contact with relevant regulatory authorities. The Director will be responsible for the oversight and management of assigned projects, with optimal efficiency, through effective performance and leadership.
Qualifications: A Master's Degree and 5 years to 7 years of experience, or an equivalent combination of education and experience, are required.
Reference Number: 40-28965
Salary Grade: 029
Employment Type: Exempt
Job Family: B-Executive/Managerial Administration