Vacancy of Clinical Research Associate (CRA)

Vacancy of Clinical Research Associate (CRA)
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Piper Companies ยท Location: United States

About the job

Piper Clinical Solutions is actively seeking a Clinical Research Associate (CRA) to join an global research organization. The Clinical Research Associate will work remotely when not on site visits and travel will remain mostly regional to their area. This person should be in Central, Midwest, or West Coast regions. CRA’s will work traditional hours, Monday – Friday.

Responsibilities of the Clinical Research Associate:

  • Monitor regional investigational sites, focusing on data integrity, and patient safety by following specific regulations
  • Plans for and executes on-site qualification, study initiation, interim monitoring, and close-out monitoring visits at investigator sites in accordance with the clinical monitoring plan.
  • Trial Master File (TMF) / Electronic Trial Master File (eTMF) management
  • Review designated site documents and validates accuracy and provide updates as necessary
  • Maintain communication with study teams and management

Qualifications of the Clinical Research Associate:

  • 3 or more years of monitoring experience within a Clinical Research Organization (CRO), academic site, or pharmaceutical organization
  • Understanding of current FDA, ICH/GCP regulations
  • Ability to travel
  • Numerous therapeutic areas accepted

Compensation for the Clinical Research Associate:

  • Salary Range: $68-80/hr., depending on years of monitoring experience and years of experience at a CRO
  • Full Benefits: Medical, Dental, Vision, 401k, PTO

Keywords: clinical research associate, CRA, senior, senior CRA, trial, site monitoring, regulatory, ICH, GCP, CRO, clinical research organization, Trial Master File, TMF, study initiation, study start up, qualification, patient study, pharmaceutical, study coordinator ย 

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