Sr. Clinical Research Associate

Clinical United States


Description

Responsible for day-to-day oversight of site management activities in the U.S. following good clinical practice and all applicable regulations.  This position will work collaboratively with Contract Research Organization that may be partnering with Inari.

Responsibilities

  1. Perform all aspects of site selection, site management, and site monitoring from start to closure of a clinical trial
  2. Use site metrics to maintain/improve recruitment, enrollment and retention
  3. Develop all study documents necessary for trial execution
  4. Contribute to drafting of protocols, patient informed consent forms and case report forms
  5. Present study related topics to audiences
  6. Manage payments to sites
  7. Work independently and prioritize study related activities
  8. Travel as needed to clinical sites
Qualifications
  1. Bachelor’s degree required
  2. 7 or more years of experience in executing and/or monitoring medical device clinical trials
  3. Experience with Microsoft programs
  4. Proficient with electronic databases used for clinical trials
  5. Experience in medical device trials preferred
  6. Experience in vendor management
  7. Able to work independently and in remote settings