Clinical Research Associate

Now Hiring: Clinical Research Associate

Location: Acton, MA (Remote)

Pay Rate: $63-$64 per hour

Duration: 6-month contract (possible extension)

Travel: Up to 60% (domestic & international)

A growing clinical research organization is seeking an experienced Clinical Research Associate (CRA / Monitor) to support domestic and international clinical trials. This contract opportunity is ideal for a detail-oriented CRA with strong monitoring experience who thrives in a fast-paced, GCP-compliant environment.

Key Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols and regulatory requirements
• Partner with senior CRAs and clinical team members to support clinical trial execution
• Train investigative site staff on protocol requirements, source documentation, and CRF completion
• Monitor clinical trial sites to ensure:
  
  
  
  • Protocol compliance
  • Accurate and complete source data documentation
  • Timely and appropriate reporting
  
  
  
  
• Support IRB submissions, including site-specific consent and assent documents
• Maintain accurate, real-time filing of site documentation within the Trial Master File (TMF)
• Ensure compliance with ICH-GCP, SOPs, and local/global regulatory requirements
• Participate in study team meetings, document meeting minutes, and track action items
• Provide study support for clinical study reports and validation activities as needed
• Collaborate cross-functionally with internal stakeholders and external study sites

Required Qualifications

• Bachelor's degree (B.S. or B.A.) or equivalent combination of education and experience
• Minimum 3 years of Clinical Research Associate (CRA) or clinical monitoring experience
• Strong knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes
• Ability to independently manage travel schedules with up to 60% travel
• Excellent attention to detail, analytical thinking, and organizational skills
• Strong interpersonal and communication skills
• Comfortable working in a remote, fast-paced clinical research environment

Skills & Competencies

• Clinical monitoring and site management
• Regulatory compliance and documentation
• Trial Master File (TMF) maintenance
• CRF and source document review
• Microsoft Word, Excel, databases, and internet-based systems
• Ability to prioritize tasks and meet deadlines
• Team-oriented with strong problem-solving abilities

Employee Benefits

Medical, dental, vision, and pet insurance | 401(k) Retirement Savings Plans | Employee Assistance Program (EAP) | Commuter/Parking Accounts | People Perks | Health Savings Account (HSA) | AD & D Insurance

Apply today to be considered for this Clinical Research Associate opportunity based in Acton, MA.

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