Join a nationwide health services organization as an Oncology Clinical Quality & Compliance Auditor.  The company's corporate office is in Houston, but the position will be field-based anywhere in the US. 

RESPONSIBILITIES:

• Conducts research site audits for adherence to GCP, ICH and FDA requirements and for timeliness and quality of clinical research data on investigator-initiated trials.
  
• Monitors compliance with written research operating procedures.
  
• Validates raw data from patient charts and audits for accuracy.
  
• Audits case record to determine if tests are completed in accordance with protocols.
  
• Audits information on CRFs to ensure consistency with medical records.
  
• Reviews site audit reports and works with research operations managers on action plans.
  
• Completes and submits research QA site audit reports.
  
• Develops and implements corporate-wide research QA programs.
  
• Responsible for new research site qualification.

QUALIFICATIONS:

• Bachelor’s degree in a clinical discipline, BSN preferred.
  
• 5+ years experience in oncology clinical research, CCRA or CCRC.
  
• Experience with collecting and reviewing data for clinical research studies.
  
• Work will require significant travel approximately 80% of workweek, on average.

Please respond with a copy or your resume as a Word document to franke@albrecht-assoc.com