Clinical Research Associate (CRA) -Multiple Locations


Perm Salary

Advanced Clinical is currently seeking a Clinical Research Associate (CRA) responsible for conducting monitoring activities at a clinical site(s) for a clinical trial(s) multiple projects and must be able to work both independently and in a team environment.


  • Follow Standard Operating Procedures (SOPs).
  • Travel to research sites as needed.
  • Attend project-specific training and client meetings as needed for the clinical trial.
  • Create materials as needed to successfully execute assigned responsibilities.
  • Perform source data verification, review regulatory documents and test article, assess protocol and regulatory compliance, and prepare trip reports as outlined in the Monitoring Plan.

Job Requirements:

  • Bachelor’s Degree, business or science/healthcare preferred
  • 1-3 years of monitoring experience or combination of on-site monitoring and clinical research experience or education; CRA monitoring experience in multiple therapeutic areas; industry certification preferred
  • Ability to perform national travel depending on project needs
  • Excellent verbal and written. communications skills; excellent interpersonal and organizational skills with demonstrated attention to detail
  • Computer literacy with proficiency in MS Office including Word, Excel, and PowerPoint

Advanced Clinical is an Equal Opportunity Employer, M/F/D/V.

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