Clinical Research Associate Minnesota

FloodGate Medical•Tampa, FL
•Remote

About The Position

Mobius Medical is hiring a Clinical Research Associate or Senior Clinical Research Associate to support medical device clinical studies. The role is based in the Minneapolis, Minnesota area and is remote with travel. Mobius is a medical-device-focused CRO operating in the USA, Australia, and New Zealand, with a lean, growing U.S. team and a portfolio spanning multiple therapeutic areas. The CRA serves as the primary site manager across a variety of device studies and owns study execution from planning and startup through monitoring and closeout. The position offers autonomy, accountability, and visibility with sponsors and company leadership, and includes contributing to the development of Mobius’s growing U.S. operations. The CRA partners with clinical operations leadership to shape project portfolios, monitoring schedules, and scope, and performs work in accordance with Mobius SOPs, study plans, GCP, and applicable regulations. The position involves regular travel, typically one to two trips per week depending on project needs. Compensation is a competitive base salary determined by experience. Benefits include medical, dental, and vision coverage, with the company paying 70% of the premium; 160 hours of PTO and 48 hours of sick leave annually; and a 401(k) with a 4% match.

Requirements

  • Bachelor’s degree in life sciences or a related field; clinicians who have transitioned into clinical research are encouraged to apply.
  • At least 3 years of CRA experience in medical devices.
  • Working command of the clinical trial lifecycle, including FDA and IDE studies, IRB submissions, TMF, GCP, site management, monitoring, and audit readiness.
  • Comfort using EDC, CTMS, and study-specific systems and tools.
  • Self-starter who asks questions, challenges the team when appropriate, and is comfortable wearing multiple hats.
  • Strong communication skills with sponsors, sites, and internal teams.
  • Comfort with regular travel, typically one to two trips per week depending on the project.

Nice To Haves

  • Cardiovascular device experience.

Responsibilities

  • Own clinical trial execution from planning and startup through monitoring and closeout.
  • Partner with the VP and Manager of Clinical Operations to shape the project portfolio, monitoring schedules, and scope.
  • Execute studies in line with Mobius SOPs, study plans, GCP, and applicable regulations.
  • Build trusted relationships with investigators and site teams, supporting high-quality data and strong compliance.
  • Troubleshoot site and study issues and find compliant, practical solutions.
  • Run regular project meetings and manage status reporting to sponsors.
  • Support budgeting, timekeeping, and billing.
  • Mentor colleagues and share knowledge as the team grows.
  • Continue professional development through ongoing training.

Benefits

  • Medical, dental, and vision coverage, with the company paying 70% of the premium.
  • 160 hours of PTO annually.
  • 48 hours of sick leave annually.
  • 401(k) with a 4% match.
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