Clinical Research Coordinator A (Department of Radiology)
HUP, United States
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Posted Job Title
Clinical Research Coordinator A (Department of Radiology)Job Profile Title
Clinical Research Coordinator AJob Description Summary
This position's primary function is to facilitate, promote, and ensure good clinical practice in the conduct of all research protocols in the Department of Radiology/Interventional Radiology. Independently coordinates and manages different tasks of complex clinical trials and mentors Coordinators and Research Assistants. Participates in study team meetings, disease site group meetings, and ongoing protocol training/compliance meetings. Adheres to all University and other regulatory guidelines.The clinical trials will be conducted at Penn Presbyterian Medical Center (PPMC) and Hospital of the University of Pennsylvania.
Overall job description.
The Clinical Research Coordinator A (CRC-A) will report directly to the Project Manager within the Interventional Radiology division of the Clinical Imaging Core. The CRC-A will have the following responsibilities: 1) Coordinate patient activities on DVT protocols: serve as primary study contact for providers, track patient referrals, screen patients for study eligibility, coordinate enrollment, schedule study visits and procedures, attend procedures, ensure all data points are collected, 2) Track enrolled study participants throughout the protocol follow up period, offer participants optional follow up procedures per protocol windows, collect follow-up specimens as outlined above and …
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Hybrid Eligible Hybrid work schedule Non-traditional work hours
Benefits/PerksCompetitive benefits package Excellent healthcare Excellent healthcare and tuition benefits Generous retirement benefits Health and wellness programs Healthcare Healthcare and tuition benefits Healthcare Benefits Hybrid work Hybrid work schedule Professional development Professional development opportunities Retirement benefits Supportive work and family benefits Tuition benefits Wellness programs Work and family benefits Work-life balance
Tasks- Regulatory submissions
Behavioral health Clinical Research Clinical trials Communication Compliance Database Management Data Management Documentation Mentoring Monitoring Patient Coordination Regulatory Compliance Research Research Protocols
Experience2 years
Education TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9