Medical Director / Snr Director, Medical Monitor - Ophthalmology Job at i-Pharm Consulting, West Virginia

  • i-Pharm Consulting
  • West Virginia

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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Job Tags

Full time, Remote work

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