Clinical Research Coordinator

3 weeks ago


Rockville, Minnesota, United States Axle Full time
Job Overview

Axle is seeking a highly skilled Clinical Research Coordinator to join our dynamic team. The ideal candidate will have a strong background in clinical research and experience in developing clinical research protocols and informed consents.

Key Responsibilities:

  • Develop clinical research protocols and informed consents for evaluation of investigational vaccines and monoclonal antibodies.
  • Conduct background research on infectious diseases targets and review and interpret scientific data and technical information.
  • Draft protocol and informed consent documents in close collaboration with the trial principal investigator and other members of the clinical research team.
  • Ensure compliance with regulatory requirements for clinical research and adherence to established protocol development timelines.

Requirements:

  • Ph.D. and/or M.D. with at least one year experience in clinical research or in a related field.
  • Master's degree with at least 3 years of experience in clinical research or in a related field.
  • Prior experience managing a team preferred.

What We Offer:

  • Market-competitive salary with an anticipated base compensation range of $68,000—$85,000 USD.
  • Benefits package including 100% medical, dental, and vision coverage for employees.
  • Paid time off, including holidays.
  • Employee referral bonus.
  • 401K match.
  • Tuition reimbursement and professional development opportunities.

Equal Opportunity Employer:

Axle is an equal opportunity employer and welcomes applications from diverse candidates. We are committed to providing a work environment that is free from discrimination and harassment.



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