Full-Time

Project Manager

Research Support

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Business & Strategy (1)
Required Skills
Ruby
Data Analysis
Requirements
  • Bachelor’s degree in relevant field
  • Minimum 3 years of relevant experience, 5 years of experience preferred
  • Experience with Human Subjects' Research required
  • Project management skills
  • Demonstrates excellent problem-solving skills and critical analyses abilities
  • Willing to work in a highly collaborative environment
Responsibilities
  • Aids in the evaluation of problems with workflow, organization, and planning and develops appropriate analytical approaches
  • Maintains multiple protocol books and chronicles manuscript preparation
  • Performs analyses of computerized datasets using standard packages to import, update, and manipulate datasets
  • Oversight of research portfolio, ensuring that research protocols are executed appropriately
  • Prepare IRB submissions and manage interactions with the central IRB for the Consortium’s portfolio of studies
  • Develop research instruments (protocol specific source documentation, lab forms, and template notes) necessary for study execution if needed
  • Oversee internal and external processes related to each study’s deliverables in accordance with the associated grant and/or contract expectations, timelines, and terms
  • Establish and update timelines and processes to guide implementation of protocols
  • Maintain databases of deliverables and reporting requirements for all active research projects, proposal-related documents/information (biosketches, SOPs, facilities, etc.)
  • Meet regularly with principal investigator(s), and protocol team leaders to review patient participation, data accuracy and overall project progress
  • Control quality of source documentation and research integrity
  • Detect and help solve logistical, technical, and patient related problems as they pertain to protocol participation
  • Coordinate laboratory specimen processing and handling with appropriate lab supervisors
  • Act as liaison between the Neuromuscular Division and other departments/centers/institutes as necessary for protocol implementation and execution
  • Participates in internal study reviews and assures compliance with outside monitoring
  • Responsible for up-to-date knowledge of UM systems associated with research management
  • 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
  • Provides timely research reports to the PI/Administrator
  • Assist with coordination of specific research studies as needed
  • Meet with, and coordinate activities related to industry-sponsored clinical trials
Desired Qualifications
  • Master’s degree or Doctorate degree from an accredited institution with clinical research experience preferred
  • Clinical Research Coordinator certification preferred
  • Minimum 5 years of relevant experience preferred

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