Director – Medical Affairs (FullTime)

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Increasing clinical development activities related to:

• NDA and pre-launch activities
• Expanding DME program
• Phase 3b/4 AMD program
• Additional clinical indications for Macugen

Summary

• Design and conduct clinical trials.
• Write protocols.
• Oversee writing of investigator brochures, annual reports, and study reports.
• Prepare for meetings with Health Authorities.
• Prepare submissions for Health Authorities.
• Provide input to Drug Safety and Surveillance Team.
• Provide input to Discovery and Pre-Clinical Team
• Provide input to Commercial Team.

Qualifications

• MD, OD, PhD, or PharmD with at least 5 years of pharmaceutical in clinical trial design and conduct.
• Strong interpersonal and leadership skills.
• Strong verbal and written communication skills.
• Meticulous and self motivated.
• Ophthalmology experience a plus.