Clinical Research Coordinator B/C

Requirements

• Bachelor of Science and 2 to 3 years of experience or equivalent combination of education and experience is required.
• Clinical Research Coordinator C
• Job Responsibilities
• Data entry - complete source documents and worksheets and complete and/or enter all clinica

Benefits

Additional Information

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. As an employer Penn has been ranked nationally on many occasions with the most recent award from Forbes who named Penn one of America's Best Large Employers in 2023. 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 B/C Job Profile Title Clinical Research Coordinator B Job Description Summary Clinical Research Coordinator B Responsible for implementing clinical research activities within the Cardiovascular Division of PPMC Responsible for assisting with study coordination and recruitment for industry sponsored studies. Works directly with study physicians, research director and other research staff. Major duties include screen/enroll patients, conduct follow-up assessments, data collection and use of EDC systems, assessment of adverse events. This coordinator will assist in ensuring patient and data safety, manage samples and related processing, and will be a proactive communicator with the team and its PIs. Clinical Research Coordinator C Responsible for implementing clinical research activities within the Cardiovascular Division of PPMC. Responsible for assisting with study coordination and recruitment for industry sponsored studies. Works directly with study physicians, research director and other research staff. Performs screening visits, consenting of participants, processing and shipping of labs, entering data into databases, escorting participants to other testing/procedure areas.. . Coordinate several investigational device trials in the cath lab, instruct and support investigators and study staff on carrying out clinical protocol and other study related requirements. Job Description This position is contingent upon favorable funding. Clinical Research Coordinator B Job Responsibilities Assist in coordinating the conduct of assigned clinical trials performed by the physicians of Penn Cardiology and collaborates with principal investigators to assure research activities are conducted with the currently approved protocol/amendments, according to Good Clinical Practice (GCP) guidelines applicable federal and state requirements and University policies. Provides oversight of administration of medications, study drugs or study interventions and monitor subject care and status throughout the course of the study. Creates and maintains research data, regulatory files, subject data and patient tracking databases. Assures reported trial data are accurate, complete and verifiable from source documents; collects data on adverse events and reports serious adverse events according to regulatory requirements. Prepares all documents for IRB review including draft informed consents written for subject reading levels. Assist in conducting in conducting initiation, monitoring and closeout visits with sponsors . Provides training and education for patient care staff in all aspects of trial initiation, conduct and closure. Serves as primary contact for subjects, sponsors and staff of research related University offices and hospital departments in nursing, pharmacy, billing, medical records related to assign studies. Travel to attend investigator's meeting presented by study sponsors.

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