November 28
• Manages cross functional project teams derived from the groups within clinical development to deliver a high-quality clinical trial(s) in compliance with all regulations and SOPs. • Works with functional areas on initiating, planning, executing, controlling, closing and resourcing clinical trial projects. • Prepares high-quality reports (financial, project, etc.) for management on program status and issues. • Ensures review of clinical electronic Trial Master File (eTMF) for completeness. • Clear and sustained demonstration of Ora’s values -- prioritizing kindness, operational excellence, cultivating joy and scientific rigor.
• Bachelor's degree in Life Science with at least 5 years of clinical trial experience. • Minimum of 1 year of clinical project management experience • Ophthalmology experience preferred. • Understanding of multi-center drug and/or device trials. • Experience with Veeva TMF and CTMS systems.
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