Principal Investigator (Virtual)

Added
7 minutes ago
Type
Full time
Salary
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Related skills

clinical research patient safety md do regulatory compliance

πŸ“‹ Description

  • Provide overall medical oversight and review of clinical trials in accordance with study protocols
  • Review sponsor-provided safety reports and assess participant safety throughout the course of
  • Review and maintain accurate case report forms and other required clinical documentation.
  • Protect the safety, wellbeing, and rights of all clinical trial participants under the
  • Assess participant responses to therapy and evaluate, document, and address adverse experiences.
  • Perform physical assessments, examinations, and study-specific clinical procedures when required by

🎯 Requirements

  • MD or DO degree with an active, unrestricted medical license valid in the state where the research
  • Previous experience serving as a Principal Investigator; approximately 2 years of Principal
  • Training and certification in Good Clinical Practice (GCP).
  • Strong understanding of clinical research processes, study protocols, participant safety, and
  • Excellent written and verbal communication skills.
  • Strong critical-thinking and dynamic problem-solving abilities.

🎁 Benefits

  • Fully remote position within the United States.
  • Part-time schedule designed for flexible involvement in clinical research.
  • Less than 10% travel, with occasional planned travel potentially required.
  • Expected compensation range: $200,000-$400,000 USD annually for full-time team members.
  • Paid time off and company-paid holidays for eligible full-time employees.
  • Employer-paid medical, dental, and vision insurance plan options for eligible full-time employees.
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