About this role

Participate in the development, conduct and reporting of corporate/global clinical trials
Understand and keep updated with the pre-clinical and clinical data relevant to the product(s)
Collaborate with the appropriate leaders in the development and maintenance of clinical strategy
Plan, collaborate on, and review the scientific content of clinical documents such as protocols, informed consent documents, final study reports, and submissions
Monitor patient safety during the conduct of studies and conduct the appropriate tracking and follow-up of adverse events
Participate in development and review of label changes and labeling modifications

Medical Doctor; must be board-eligible or certified in appropriate specialty/subspecialty
At least 5 years clinical research or pharmaceutical medicine experience desirable
Demonstrated knowledge of drug development process
Fluent in English; both written and verbal communications
Demonstrated strong communication, interpersonal, organizational, teamwork and negotiation skills
Demonstrated ability to influence others (both cross-functionally and within the function)

Medical, dental, vision and prescription drug benefits
Flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
Life insurance and death benefits
Company-sponsored 401(k)
Pension benefits
Vacation benefits
Certain time off and leave of absence benefits
Well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)

Clinical Research Physician – Ophthalmology

Key skills