Vincent, East Pavilion, 6th Floor Sylvan Hill, Highlands Building, 2nd Floor Experience in Ophthalmology highly desirable. Required Education – Bachelor’s degree, or an associate degree with two years relevant research experience required.Įxperience – Combined experience of clinical research along with education. Required knowledge, skills, abilities: EHR experience preferred (NextGen experience desirable) excellent communication and interpersonal skills 45+ WPM flexibility and adaptability critical thinking detail oriented critical thinking team focus. Attend executive director approved investigator meetings and conferences, representing RNW in a professional manner, and act appropriately at all times. Order and maintain drugs and supplies for studies. Maintain adequate medical supplies and investigational products required for the study. Maintain exam rooms for necessary supplies and materials in accordance with RNW policy/process. Coordinate all study activities including scheduling patient appointments and acting as a liaison between physicians, the sponsor and Sylvan clinic staff (Routinely meet with physicians and Sylvan Clinical Site Supervisor to streamline research patient flow). Maintain thorough knowledge of informed consents. Instruct patients regarding study, protocols, and procedures. Communicate with physicians and staff to apprise them of changes in study protocols. Obtain patient histories and performs refractions, EKGs, visual acuities, tonometry and other tests according to study protocols. Takes personal initiative, exhibits self-motivation, and must be able to coordinate multiple projects simultaneously. Submits regulatory documents on the behalf of the clinic site and assists in the resolution of issues to IRB submissions and the approval process throughout the study. Establishes and maintains working relationships with RNW staff, local and central IRBs. Assures that RNW fulfills all requirements of studies, obtains study specific essential documentation and required materials from the sponsor, and ensures that all requirements are documented in the regulatory binder and implemented consistently throughout the trial. Creates, reviews, maintains and updates protocols, brochures, advertisements, informed consents, SOPS, the research intranet, subject information templates and patient files. Develops Research Fee Slips specific to each study working alongside the Business Services Lead and Patient and Business Services Manager. Works in collaboration with physicians to identify, prescreen and recruit eligible patients. Access to reliable transportation is required to support.Ĭlinical Research Coordinator Description : Assures that RNW fulfills all requirements in accordance with all applicable governing regulations to ensure the rights and protection of human subjects in clinical trials. Competitive Salary, 100% paid employee premiums for medical/dental/vision/LTD/Life benefits, Holidays, a flexible Paid Time-Off (PTO) program, 401K, and either free or paid parking at all locations. The position of Clinical Research Coordinator is Full-time, exempt, and benefited, working Monday-Friday at our Sylvan clinic. RNW Core Values ~Īccountability Compassion Continuous Improvement Customer Focus Integrity Quality Teamwork All team members share a common commitment to serve our patients and each other with an emphasis on respect, consideration, and care. Retina Northwest is looking for teammates who are motivated and enthusiastic to join our team in providing the highest quality specialized care in the treatment of threatening diseases and injuries of the retina and vitreous. Retina Northwest physicians and staff utilize the latest medical diagnostic and surgical treatment to provide the best possible outcome and future for our patients. Retina Northwest has been providing cutting-edge and compassionate care to patients with conditions of the retina and vitreous for over 36 years in the Portland/Vancouver community. Clinical Research Coordinator - Ophthalmology
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