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: · Conduct protocol management for an assigned set of multiple research protocols. · Conduct background check research, write and develop new clinical research protocols under the guidance of a medical
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through cutting-edge research. Exciting opportunity for a detail-oriented individual! Join us as a Clinical Research Assistant I in which you will manage an assigned set of multiple research protocols
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alignment with a given research protocol requiring EDC support. Design, develop, validate, and maintain applications used to capture eCRF data within Forte EDC. Provide programming of validation checks and
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progress internally or externally. · Ability to work in a fast-paced team environment and handle multiple projects simultaneously. Your qualifications should include: · Ph.D., MD, or MD/Ph.D
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multiple research protocols to assure efficiency and regulatory compliance of the protocol, attending clinic as needed. You will be responsible for compilation, registration and submission of data
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, implement, and maintain the process for entering summary level accrual information in OnCore and manage the data integrity across multiple clinical research systems. Additionally, you will be responsible
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management skills, with the ability to analyze trends. Excellent organizational skills, ability to manage multiple priorities and responsibilities Outstanding customer service skills Must be willing to travel
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registration. Additional duties include: generating registration visits for multiple patient types including surgical, physician office visits, patient transfers, managing both the registration hotline on a 24/7
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of Medical Oncology at both the Duarte campus and Lennar campus in Orange County. As a successful candidate, you will: · Conduct protocol management of multiple research protocols. · Maintain
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and conducting meetings Excellent organizational skills and be able to manage multiple priorities and responsibilities Efficient, reliable, flexible, goal oriented and adaptable to change, while