Sr. CRA, Sponsor Aligned, Oncology

Lifelancer
Overland Park, KS
Category Research
Job Description
Join our dynamic team as a Clinical Research Associate! You’ll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking cancer research and make a real impact on patients’ lives.

Requirements

  • Conduct site monitoring visits
  • Collaborate with sites to develop and track recruitment plans
  • Provide protocol and study training to sites
  • Assess site practices for protocol adherence and regulatory compliance
  • Oversee regulatory submissions and study progress
  • Ensure all site documents are filed in the Trial Master File (TMF) and Investigator’s Site File (ISF)
  • Generate visit reports, follow-up letters, and other necessary documentation
  • Mentor clinical staff through co-monitoring and training visits
  • Work closely with study team members to support project execution

Benefits

  • Health and welfare benefits
  • Incentive plans
  • Bonuses
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