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Clinical Trials Manager

2 months ago

Philadelphia, Pennsylvania, United States InsideHigherEd Full time

Job Summary

We are seeking a highly skilled 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