Full-Time

Manager – Clinical Research

Cardiology

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Biology & Biotech (4)
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Required Skills
Ruby
Requirements
  • Bachelor’s degree in relevant field
  • Minimum 5 years of relevant experience
  • Knowledge of business and management principles
  • Ability to direct, manage, implement, and evaluate department operations
  • Ability to establish department goals, and objectives that support the strategic plan
  • Ability to effectively plan, delegate and/or supervise the work of others
  • Ability to lead, motivate, develop, and train others
Responsibilities
  • Works with investigators and study teams to help meet targets and milestones, ensures timely and accurate submission to IRBs, sponsors and master agreements, and coordinates with the Research Program Director on remediation
  • Coordinates the efforts of relevant team members to manage, retain and control all applicable Regulatory Affairs submissions pertaining to University held INDs and IDEs as well as exemption requests
  • Assembles project plans, team and work assignments, directing and monitoring work efforts on a daily basis, identifying resource needs, performing quality review, and escalating functional, quality and timeline issues appropriately
  • Manages investigator relationships
  • Maintains IND and IDE documentation, including annual reports for delegated studies and works with the primary investigator and project team to assist in responding to queries from regulatory agencies including the FDA
  • Tracks proposals and other study relevant documentation through signature/approval processes then through collaboration with Contracts and budgets
  • Serves as liaison and facilitates meetings between project stakeholders and leadership and completes and maintains professional documentation for projects and deliverables, develops SOPs as needed, and assists in the auditing and monitoring of studies
  • Identifies areas for improvement within daily functions, internal procedures, and regulatory agency interactions
  • Interacts with project team members to define submission logistics and workflow scheduling
  • Oversees the ongoing maintenance of records detailing the number of active INDs and IDEs and related data via an internal tracking system
  • Prepares and presents the annual summary report for clinical trial and research areas
  • Provides consultation and guidance for UM held INDs and IDEs
  • Develops, implements, maintains and oversees internal policies and SOPs as well as University‐wide policies and SOPs intended to assist University researchers in maintaining compliance with FDA regulations and other Clinical Research Best Practices
  • Establishes and continuously assesses the effectiveness of the internal controls within the unit and compliance with University policies and procedures. Ensures employees are trained on controls within the function and on University policy and procedures
Desired Qualifications
  • Master’s degree preferred

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