CRA

Piper Companies is currently seeking a motivated Clinical Research Associate to work for an award winning global CRO.

Responsibilities of the Clinical Research Associate:

• Develop and maintain relationships with investigative sites and client personnel
• Monitor sites for accuracy and validity of entries related to patient records and clinical notes
• Provide and communicate trial status and progress reports to trial manager and client
• Manage and maintain the data and documents required by local and ICH regulatory authorities
• Ensure SOPs are being followed and assist with client audits and regulatory inspections
• Regional travel

Qualifications of the Clinical Research Associate:

• 2-3+ years of experience, onsite monitoring experience required 
• Experience with FDA, ICH GCP, and local regulations
• Prior experience within the therapeutic areas of Oncology
• Strong Oncology CRA -> heavy in-depth experience 
  • 2-3 days onsite (standard) 
  • Coordinator moving to CRA monitor in oncology would be ideal 
• Site initiation experience
• Bachelor’s degree or equivalent experience required

Compensation for the Clinical Research Associate:

• Salary Range: $100,000-$115,000 based on experience
• Benefits: Paid Holidays, Regional Travel, Advancement opportunities, Support one dedicated sponsor
• Per diem and internet allowance for travel