Clinical Research Associate II - Oncology WI- Remote

Added
26 minutes ago
Type
Full time
Salary
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Related skills

crm gcp regulatory knowledge clinical research site monitoring
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πŸ“‹ Description

  • Primary contact for investigative site; connect stakeholders and sites.
  • Train and motivate site staff and PI on trial goals and patient treatment.
  • Conduct site evaluation, training, monitoring per protocol and regulations.
  • Develop site engagement strategies; report progress using CRM tools.
  • Link protocol, science, and trial execution for recruitment and retention.
  • Mentor less experienced CRAs; participate in global/local initiatives.

🎯 Requirements

  • Tertiary qualification in health-related field preferred.
  • At least 1 year clinically-related experience; 6 months in trial monitoring.
  • Knowledge of regulatory requirements, ICH/GCP guidelines.
  • Strong collaboration, planning, organizational skills.
  • Proficiency with technology/tools for patient-centric site support.
  • Excellent communication; ability to build site partnerships.

🎁 Benefits

  • Comprehensive benefits package; PTO, medical/dental/vision insurance, 401(k).
  • Eligibility to participate in incentive programs.
  • Equal opportunity employer; diverse, inclusive environment.
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