
201 - 500 employees
💊 Pharmaceuticals
🧬 Biotechnology
💰 $135M Series E on 2021-09
Healthcare • Pharmaceuticals • Biotechnology
Elligo Health Research is a company that facilitates clinical trials by bridging the gap between research and healthcare. They provide essential tools and services such as patient recruitment, engagement, and innovative technologies, including their proprietary IntElligo® system. With access to a vast network of healthcare and research sites, Elligo supports sponsors, clinical trial sites, and patients in navigating the complex landscape of clinical research across a wide range of therapeutic areas.
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201 - 500 employees
💊 Pharmaceuticals
🧬 Biotechnology
💰 $135M Series E on 2021-09
Healthcare • Pharmaceuticals • Biotechnology
Elligo Health Research is a company that facilitates clinical trials by bridging the gap between research and healthcare. They provide essential tools and services such as patient recruitment, engagement, and innovative technologies, including their proprietary IntElligo® system. With access to a vast network of healthcare and research sites, Elligo supports sponsors, clinical trial sites, and patients in navigating the complex landscape of clinical research across a wide range of therapeutic areas.
• Support the successful performance and operations of Elligo’s clinical trials. • Serve as a liaison between multiple departments to ensure project tasks are tracked and/or completed. • Coordinate collection and submission of all regulatory related documents. • Obtain and review required medical records, data entry, and other various project support tasks. • Perform set-up, maintenance and close out project files and study information. • Works within forecasted submission/approval timelines and tracks milestone progress. • Prepare and complete the preparation of regulatory documents required for IRB/IBC approvals. • Assist with coordination of team meetings, attend meetings, and prepare accurate meeting minutes.
• BS/BA in Life Science or related discipline. • Minimum of one (1) year clinical research experience (including Study Coordinator, CRO experience) or working in a healthcare setting. • Previous GCP training and certification is preferred. • Experience working with electronic medical records (EMRs); electronic health record system proficiency is preferred. • Data entry experience is preferred.
• Fully Remote
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