Ideal Background MD with specialist training in Ophthalmology Board-certified or board-eligible Ophthalmologist Proven hands-on Medical Monitoring experience in Ophthalmology Minimum 3 years of clinical practice treating ophthalmology patients 1+ years of pharmaceutical or CRO Medical Monitoring experience in Ophthalmology Experience supporting Phase II / III clinical trials CRO experience preferred, although sponsor-side candidates with strong Medical Monitoring experience will be considered Experience across ophthalmology indications, particularly: Wet AMD Dry AMD Thyroid Eye Disease Other front-of-the-eye and back-of-the-eye indications What You’ll Do Serve as Medical Monitor for assigned ophthalmology clinical studies Provide medical oversight of subject safety, clinical data, and study delivery Act as a key medical contact for sponsors, investigators, and internal study teams Review clinical and safety data and identify emerging trends, risks, and mitigation strategies Partner with Drug Safety / Pharmacovigilance and cross-functional clinical teams Provide medical input into protocols, study materials, feasibility, and study start-up Deliver therapeutic training and occasionally support investigator meetings, RFPs, and bid defenses Compensation & Working Model Director: $250,000 – $290,000 base + bonus + benefits Senior Director: $270,000 – $315,000 base + bonus + benefits Fully remote – United States Occasional travel: approximately 3–5 times per year Final level and compensation determined based on experience, scope, and overall fit Job Description: Director / Senior Director Medical Monitor– Clinical Development, Ophthalmology Remote | United States | Full-Time About the Role A hands-on Clinical Development / Medical Monitoring opportunity within a highly regarded global life sciences organisation supporting actively running ophthalmology clinical trials.