Clinical Trials Project Coordinator - Vitalograph

Benefits:

• 401(k)
• Employee assistance program
• Health insurance
• Paid time off
• Professional development assistance
• Tuition reimbursement

We are seeking a customer focused and proactive Project Co-Ordinator to join our Clinical Trials team in Lenexa, KS. We offer a flex schedule, opportunities for international travel and exciting development opportunities. Due to expansion and growth in the market, now is a very exciting time to become part of our team.

Vitalograph is the world's leading manufacturer of medical respiratory diagnostic devices and software for 60 years! Headquartered in the UK, VItalograph has operations in Ireland, Germany and the USA.

Responsibilities as a Clinical Trials Co-Ordinator:

      Assisting the project Management Team with general study duties

      Assisting the Project Manager with the monitoring for GCP compliance within centralized clinical trials

      Reporting on study progress

      Problem solving project issues

      Assisting with training Monitors and Investigators

      Writing study related documents as requested by Project Team

      Assisting with writing, updating and printing study manuals

      Gathering information on Pharmaceutical and Biotech companies (as required) to assist other members of Vitalograph team with sales opportunities

      Attending conferences on behalf of Vitalograph in a sales capacity

     Ensuring any study related documents are filed and stored appropriately

Requirements as a Clinical Trials Co-Ordinator:

      Organizational skills and the ability to use project management tools

      Previous experience in a clinical trials environment is preferred

      Understanding of GCP*

      Proficient on Microsoft Office applications

Educational Requirements:

High School Diploma or GED

Associate's Degree or higher