Clinical Res Project Mgr Hlth Job Description Template
Our company is looking for a Clinical Res Project Mgr Hlth to join our team.
Responsibilities:
- Prepare appropriate reports on each research patient, maintaining and completing the supplied case report forms for investigator and/or sponsor;
- Supervise the scheduling and the collection, processing and analysis of data;
- Screen and have oversight for the recruitment of subjects per study protocol;
- Coordinate the handling of study medications;
- Design work flow and participate in quality assurance measures and coordinate study site visits;
- Assist in the reporting of test results (36%);
- Collects and manages patient and laboratory data for clinical research projects;
- Build and maintain regulatory binders for each study;
- Write Clinical Trial Protocols and Abstracts/Manuscripts (17%);
- Lead and participate in conferences related to the project and/or its progress;
- Submit Data Safety reports to the Data Safety Management Board and IRB;
- Collect specimens, monitor subjects and ensure patient’s response to therapy is adequate to continue on study;
- Facilitate audits from sponsor institutions or internally (32%);
- Consent research participants for clinical research studies/trials;
- Create and manage required clinical research billing calendars.
Requirements:
- Master’s Degree in Public Health or Epidemiology;
- Reasonable knowledge of University research policies, procedures and computer systems;
- Experience with multi-institutional protocols;
- Experience in healthcare and/or academia;
- Experience with Pediatric Oncology/BMT/Complex Patient Care;
- Experience with the University of Michigan’s eResearch system;
- Experience with mobile health app projects.