Clinical Research Associate - 119425

Format: 3-6 month contract-to-hire Our client is is hiring a Senior Clinical Research Associate (Sr. CRA) to oversee ophthalmic medical device trials for dry Age-Related Macular Degeneration (AMD). The remote, Midwest-based role requires 4+ years of medical device monitoring experience, ophthalmology expertise, and 50% to 60% travel. Key Responsibilities Site Management: Evaluate and select clinical investigators, conduct qualification, initiation, interim, and close-out visits. Compliance & Monitoring: Ensure trial compliance with ICH GCP guidelines, Declaration of Helsinki, and FDA regulations. Training: Provide on-site and remote training to clinicians on the use of the proprietary bioelectric stimulation device. Documentation: Manage Trial Master File (TMF) documents, site visit reports, and promptly escalate any protocol deviations. Recruitment: Collaborate with recruitment teams to develop patient materials and identify study participants. Requirements Experience: 4+ years of clinical research study monitoring for medical devices. Specialty: Ophthalmology experience is highly preferred. Education: Bachelor of Science (BS) degree or equivalent experience. Location & Travel: Home-based in the Midwestern USA with the ability to travel frequently (50% to 60%).