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Project Manager, Research Support
Company | University of Miami |
Address | Miami, FL, United States |
Employment type | FULL_TIME |
Salary | |
Category | Higher Education |
Expires | 2023-08-29 |
Posted at | 9 months ago |
Current Employees:
- Develop research instruments (protocol specific source documentation, lab forms, and template notes) necessary for study execution if needed
- Participates in internal study reviews and assures compliance with outside monitoring
- Meet regularly with principal investigator(s), and protocol team leaders to review patient participation, data accuracy and overall project progress
- Detect and help solve logistical, technical, and patient related problems as they pertain to protocol participation.
- Provides timely research reports to the PI/Administrator
- Establish and update timelines and processes to guide implementation of protocols
- Work closely with PI and Administrator in performing activities associated with a grant close-out (i.e., accounting, final reports, record archive, web site closure
- Act as liaison between the Neuromuscular Division and other departments/centers/institutes as necessary for protocol implementation and execution
- Oversee internal and external processes related to each study’s deliverables in accordance with the associated grant and/or contract expectations, timelines, and terms
- Oversight of research portfolio, ensuring that research protocols are executed appropriately
- Assist with coordination of specific research studies as needed.
- Coordinate laboratory specimen processing and handling with appropriate lab supervisors.
- Maintain databases of deliverables and reporting requirements for all active research projects, proposal-related documents/information (biosketches, SOPs, facilities, etc.)
- Prepare IRB submissions and manage interactions with the central IRB for the Consortium’s portfolio of studies
- Control quality of source documentation and research integrity
- Meet with, and coordinate activities related to industry-sponsored clinical trials
- Responsible for up-to-date knowledge of UM systems associated with research management
- Master's degree or a Doctorate degree from an accredited institution with clinical research experience preferred.
- Grants management experience.
- Experience with Human Subjects' Research, highly preferred.
- Strong research background with publication experience.
- Bachelor’s degree in relevant field.
- Must be very adoptable and change projects instantaneously.
- Willing to work in a highly collaborative environment.
- Project management skills.
- Clinical Research Coordinator (or similar) certification preferred.
- Demonstrates excellent problem-solving skills and critical analyses abilities
- Minimum 3 years of relevant experience
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