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Philadelphia, Pennsylvania, United States University of Pennsylvania Full timeJob Title: Clinical Research CoordinatorUniversity OverviewThe University of Pennsylvania, a world-renowned leader in education, research, and innovation, is seeking a highly skilled Clinical Research Coordinator to join its team. As a member of the Perelman School of Medicine, this individual will play a critical role in managing mixed methods and...
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Clinical Research Coordinator B
6 days ago
Philadelphia, Pennsylvania, United States Trustees of University of Pennsylvania Full timeJob SummaryThe Clinical Research Coordinator B will assist in the management of multiple clinical trials and will be responsible for study coordination for industry studies, investigator-initiated studies, and multi-center research studies. They will facilitate, promote and ensure good clinical practice in the conduct of all research protocols in the...
Clinical Research Coordinator
2 months ago
Job Summary
We are seeking a highly skilled and experienced Clinical Research Coordinator to join our team at InsideHigherEd. The successful candidate will be responsible for coordinating Phase I-IV clinical trials, recruiting and consenting patients, and ensuring adherence to protocol requirements.
Key Responsibilities
- Coordinate clinical trials, including recruiting and consenting patients, scheduling patient visits, and monitoring patient data
- Organize and maintain all documentation required by sponsors or CROs, including source documentation, case report forms, and research charts
- Collect, review, and report study data, complete case report forms, and resolve data queries
- Process and ship study specimens, including blood, urine, and tissue samples
- Participate in initiation, monitoring, audit, and close-out visits, as well as study team meetings and disease site group meetings
- Assist in the development and maintenance of study-specific case report forms and source document tools
- Show vigilance in patient safety, protocol compliance, and data quality
Requirements
- Bachelor's degree and 2-4 years of related experience or an equivalent combination of education and experience
- Effective problem-solving abilities, effective communication and writing skills, strong organizational and time management skills
- Flexible and able to multi-task, demonstrated ability to work as part of a team, as well as independently
- Knowledge of IRB and human research protection regulations
Special Requirements
- Background check required after a conditional job offer is made
Job Family
I-Technical/Professional Research