About the role

To support innovative clinical trials in Ophthalmology, the part-time contract Ophthalmology Medical Monitor will provide medical monitoring and study startup activities, advise on clinical trial-related medical questions, and ensure compliance with safety protocols while working remotely.
Key responsibilities: Provide medical monitoring and support for 1-3 Ophthalmology programs under the direction of the Global Medical Lead Review and analyze eligibility of participants, adverse events, and ensure compliance with regulatory requirements Develop and review operational, medical monitoring, and safety plans, and generate safety-related documentation
Required qualifications: Medical Degree with completion of residency in Ophthalmology and active or prior Board Certification At least 8 years of relevant experience in drug development within a biotech/pharmaceutical company or academic clinical research institute Excellent scientific writing skills and experience analyzing clinical trial data Proficiency with ICH/GCP guidelines and understanding of medical terminology and clinical research Willingness to work across different ophthalmic indications

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JOB OVERVIEW

Experience level

Senior

Location

New York, NY

Occupation

Ophthalmic Medical Technicians

Industry

Offices of Physicians (except Mental Health Specialists)

Posted

8 days ago

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