• Job Description

  Req#: 53450
  Pay Rate Low: 65 | Pay Rate High: 85
  We are seeking a high-level, technically proficient Senior or Principal CRA to oversee complex monitoring activities for specialized Medical Device trials. This role requires a "hands-on" expert who possesses the deep clinical intuition and technical skills that only come with years of dedicated field experience.
  
  Job Title: Senior / Principal Clinical Research Associate (Medical Device)
  Location: Remote (Midwest or Central Time Zone preferred)
  Pay rate: $65-80/hr (Depending on experience)
  Term: 12-Month Renewable Contract (W-2 with benefits)
  Travel: Approximately 60-70% The Role
  You will manage site performance across the East Coast and Midwest, focusing on high-enrollment sites and long-term follow-up monitoring.
  Core Responsibilities
  • Conduct comprehensive monitoring visits (PSV, SIV, RM, COV) across East Coast and Midwest territories.
  • Manage a high volume of site activities, ensuring adherence to protocols, IDE regulations, and ISO 14155 standards.
  • Drive enrollment and oversee long-term patient follow-up for complex device studies.
  • Act as a primary liaison for clinical sites, fostering strong investigator relationships.
  Qualifications
  • Minimum 5+ years of CRA experience (must be at a Senior or Principal level).
  • Direct Medical Device monitoring experience is required.
  • Cardiology therapeutic experience is highly preferred.
  • Experience outside of "Big CRO" environments is preferred; we value versatile talent capable of working independently.
  • Ability to travel 60% of the time (approx. 2 weeks/month).
  • Must be based in the U.S.; Central Time Zone is a plus to bridge Eastern and Western engagements.
  INDBH
  #LI-MG1

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