University Overview The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World Report survey. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn’s distinctive interdisciplinary approach to scholarship and learning. Penn offers a unique working environment within the city of Philadelphia. The University is situated on a beautiful urban campus, with easy access to a range of educational, cultural, and recreational activities. With its historical significance and landmarks, lively cultural offerings, and wide variety of atmospheres, Philadelphia is the perfect place to call home for work and play. The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A Job Profile Title Clinical Research Coordinator A Job Description Summary This position will assist in the management of multiple clinical trials and responsibilities in specific research area. The Research Coordinator will be responsible for all aspects of clinical trails coordination including: subject recruitment, detailed data entry, subject visits and follow-up regulatory documentation. Job Description The primary role of the Clinical Research Coordinator is the organization , coordination, and implementation of research studies for the MCHRC. The essential functions of the position include but are not limited to: Detailed screening of patients for eligibility across multiple studies. Consenting of patients into multiple studies. Coordinate scheduling of trail participants visits with study investigators and nurse practitioners as per protocol. Collaborate with clinical team as necessary to provide a positive encounter. Provide clinical services, including phlebotomy and obtain biospecimens as required by the protocol. Intercept and respond to trail participants phone calls. Perform telephone follow-up per study protocol. Data collection and management in accordance with study protocol and the maintenance of source documents and case reports forms. Collect and report timely, valid accurate data, maintain individual patient records. Maintain study compliance and integrity through close collaboration with nurse practitioners and investigators as well as the patient. Position is contingent upon funding. Qualifications: Bachelor's Degree with 1- 3 years of research experience or an equivalent combination of education and experience required. Position requires a highly motivated, articulate individual with excellent oral and written communication skills. The candidate should possess the ability to work independently and also as part of a team. Strong planning, organizational and prioritizing capabilities along with problem solving skills desired. Must be able to work flexible hours. Position contingent upon funding
