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Project Coordinator

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Job DescriptionFor over 60 years, Vitalograph has been at the forefront of medical respiratory diagnostic devices and software, setting the standard globally. Headquartered in the UK, with thriving operations in Ireland, Germany, and the USA, we are expanding our dynamic team in the U.S!

The Role: Project Coordinator – Clinical Trials

Are you passionate about making a difference in healthcare? Join our Clinical Trials team as a Project Coordinator, where you'll play a crucial role in driving forward cutting-edge clinical studies. You'll work in a stunning office environment, surrounded by a team dedicated to innovation and excellence.

Why Vitalograph?

At Vitalograph, we believe in fostering a vibrant and supportive work environment. Based in Lenexa, KS, enjoy a competitive salary, excellent benefits, flexible scheduling and exciting career development opportunities.

Key Responsibilities

  • Assist Project Managers and Senior Project Managers with various study duties, ensuring seamless project execution.
  • Help maintain GCP compliance within centralized clinical trials, safeguarding the integrity and quality of our research.
  • Keep our team informed with regular updates on study progress, identifying and solving project issues proactively.
  • Aid in training Monitors and Investigators, enhancing the capabilities of our clinical team.
  • Craft, update, and manage study-related documents and manuals, ensuring accuracy and accessibility.
  • Gather insights on pharmaceutical and biotech companies, supporting our sales team's strategic efforts.
  • Ensure all study-related documents are meticulously filed and stored, maintaining a high standard of documentation.

Desired Skills

  • Strong organizational skills with the ability to effectively use project management tools.
  • Previous experience in a clinical trials environment is a plus.
  • A solid understanding of Good Clinical Practice (GCP) standards.
  • Proficient in Microsoft Office applications.

Educational Requirements

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

Ready to Make an Impact?

If you're a customer-focused, proactive individual with a passion for clinical research, we want to hear from you! Join Vitalograph and be a part of a team that's shaping the future of respiratory diagnostics. Apply now and embark on a career that's as exciting as it is rewarding.
Job DescriptionFor over 60 years, Vitalograph has been at the forefront of medical respiratory diagnostic devices and software, setting the standard globally. Headquartered in the UK, with thriving operations in Ireland, Germany, and the USA, we are expanding our dynamic team in the U.S!

The Role: Project Coordinator – Clinical Trials

Are you passionate about making a difference in healthcare? Join our Clinical Trials team as a Project Coordinator, where you'll play a crucial role in driving forward cutting-edge clinical studies. You'll work in a stunning office environment, surrounded by a team dedicated to innovation and excellence.

Why Vitalograph?

At Vitalograph, we believe in fostering a vibrant and supportive work environment. Based in Lenexa, KS, enjoy a competitive salary, excellent benefits, flexible scheduling and exciting career development opportunities.

Key Responsibilities

  • Assist Project Managers and Senior Project Managers with various study duties, ensuring seamless project execution.
  • Help maintain GCP compliance within centralized clinical trials, safeguarding the integrity and quality of our research.
  • Keep our team informed with regular updates on study progress, identifying and solving project issues proactively.
  • Aid in training Monitors and Investigators, enhancing the capabilities of our clinical team.
  • Craft, update, and manage study-related documents and manuals, ensuring accuracy and accessibility.
  • Gather insights on pharmaceutical and biotech companies, supporting our sales team's strategic efforts.
  • Ensure all study-related documents are meticulously filed and stored, maintaining a high standard of documentation.

Desired Skills

  • Strong organizational skills with the ability to effectively use project management tools.
  • Previous experience in a clinical trials environment is a plus.
  • A solid understanding of Good Clinical Practice (GCP) standards.
  • Proficient in Microsoft Office applications.

Educational Requirements

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

Ready to Make an Impact?

If you're a customer-focused, proactive individual with a passion for clinical research, we want to hear from you! Join Vitalograph and be a part of a team that's shaping the future of respiratory diagnostics. Apply now and embark on a career that's as exciting as it is rewarding.