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Clinical Trials Project Coordinator

2 months ago

Lenexa, Kansas, United States Vitalograph Full time

Benefits:

  • Competitive compensation package
  • Comprehensive benefits program
  • Employee assistance program
  • Health insurance
  • Paid time off
  • Professional development opportunities
  • Tuition reimbursement

About the Role:

We are seeking a highly organized and proactive Clinical Trials Project Coordinator to join our team at Vitalograph. As a key member of our Clinical Trials team, you will be responsible for assisting the project management team with general study duties, monitoring for GCP compliance, and reporting on study progress.

Responsibilities:

  • Assist the project management team with general study duties, including data management and reporting
  • Monitor for GCP compliance within centralized clinical trials
  • Report on study progress and provide regular updates to the project management team
  • Problem-solve project issues and provide solutions
  • Assist with training monitors and investigators
  • Write study-related documents as requested by the project team
  • Assist with writing, updating, and printing study manuals
  • Gather information on pharmaceutical and biotech companies to assist the sales team
  • Attend conferences on behalf of Vitalograph in a sales capacity
  • Ensure study-related documents are filed and stored appropriately

Requirements:

  • Organizational skills and ability to use project management tools
  • Previous experience in a clinical trials environment is preferred
  • Understanding of GCP
  • Proficient in Microsoft Office applications

Educational Requirements:

  • High School Diploma or GED
  • Associate's Degree or higher