About this opportunity
i-Pharm Consulting lists this Medical Director / Snr Director, Medical Monitor - Ophthalmology opportunity in united, West Virginia. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Job Description
Director / Senior Director Medical Monitor– Clinical Development, Ophthalmology
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Remote | United States | Full-Time
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About the Role
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A hands-on Clinical Development / Medical Monitoring opportunity within a highly regarded global life sciences organisation supporting actively running ophthalmology clinical trials.
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This is a delivery-focused role within a collaborative global medical organisation. The successful candidate will provide medical oversight across multiple ophthalmology programs, working closely with sponsors and cross-functional study teams to support subject safety, data integrity, and successful study delivery.
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The position is particularly suited to an ophthalmologist who has already worked as an industry Medical Monitor and can step directly into active Phase II/III studies.
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Ideal Background
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- MD with specialist training in Ophthalmology
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- Board-certified or board-eligible Ophthalmologist
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- Proven hands-on Medical Monitoring experience in Ophthalmology
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- Minimum 3 years of clinical practice treating ophthalmology patients
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- 1+ years of pharmaceutical or CRO Medical Monitoring experience in Ophthalmology
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- Experience supporting Phase II / III clinical trials
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- CRO experience preferred, although sponsor-side candidates with strong Medical Monitoring experience will be considered
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- Experience across ophthalmology indications, particularly:
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- Wet AMD
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- Dry AMD
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- Thyroid Eye Disease
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- Other front-of-the-eye and back-of-the-eye indications
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What You’ll Do
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- Serve as Medical Monitor for assigned ophthalmology clinical studies
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- Provide medical oversight of subject safety, clinical data, and study delivery
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- Act as a key medical contact for sponsors, investigators, and internal study teams
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- Review clinical and safety data and identify emerging trends, risks, and mitigation strategies
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- Partner with Drug Safety / Pharmacovigilance and cross-functional clinical teams
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- Provide medical input into protocols, study materials, feasibility, and study start-up
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- Deliver therapeutic training and occasionally support investigator meetings, RFPs, and bid defenses
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Compensation & Working Model
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- Director: $250,000 – $290,000 base + bonus + benefits
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- Senior Director: $270,000 – $315,000 base + bonus + benefits
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- Fully remote – United States
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- Occasional travel: approximately 3–5 times per year
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- Final level and compensation determined based on experience, scope, and overall fit
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.