Senior CRA - Contract

Piper Companies is hiring a Clinical Research Associate (CRA II/III/Senior CRA) for a global clinical research organization located in a remote setting. The Clinical Research Associate will support an ongoing project driven by an overload of work, ensuring clinical trials are conducted efficiently and in compliance with regulatory standards. This is a contract position requiring prior notice for interviews and phone-based screening. Therapeutic experience in Oncology or Ophthalmology is non-negotiable. 

Responsibilities of the Clinical Research Associate: 

• Build and maintain strong relationships with Principal Investigators, study coordinators, pharmacists, and site personnel 
• Manage and monitor clinical trial sites in accordance with ICH GCP §5.18 and study-specific Clinical Monitoring Plans 
• Conduct site visits including site selection, initiation, monitoring, and close-out (remote or onsite as required) 
• Ensure patient safety, protocol compliance, and proper reporting of adverse events/SAEs 
• Verify accuracy and completeness of trial data and resolve CRF queries within study timelines 
• Collaborate with IHCRA and regulatory teams on site documentation, submissions, and approvals 
• Drive patient recruitment strategies and ensure enrollment targets are met 
• Maintain Trial Master File (TMF) and ensure audit/inspection readiness at all times 
• Provide detailed monitoring reports and study updates to project leadership 
• Support study execution, including payment tracking and project planning with cross-functional teams 

Requirements of the Clinical Research Associate: 

• Bachelor’s degree in life sciences or a related clinical field 
• Oncology or Ophthalmology experience required (non-negotiable) 
• Experience level based on title: 
• CRA II: 1–2 years of CRA or equivalent clinical research experience 
• CRA III: 2–3 years of CRA experience 
• Senior CRA: 3–5+ years of CRA experience 
• Strong understanding of ICH GCP, regulatory requirements, and clinical trial processes 
• Ability to work in a fast-paced, high-volume project environment 
• Strong communication skills and ability to manage site relationships effectively 

Compensation for the Clinical Research Associate: 

• Competitive hourly rate (based on experience level) 
• Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law 

Keywords: 

Clinical Research Associate, CRA II, CRA III, Senior CRA, Oncology, Ophthalmology, ICH GCP, Clinical Trials, Monitoring, Regulatory, Remote, Contract 

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This role becomes available for applicants on 7/29/2026 and will remain open for at least 30 days from the listed posting date.