Medpace - Denver, CO

posted about 2 months ago

Full-time - Entry Level
Remote - Denver, CO
1,001-5,000 employees
Professional, Scientific, and Technical Services

About the position

The Project Coordinator at Medpace plays a crucial role in the Clinical Trial Management team, focusing on the management of clinical trials across various therapeutic areas including Oncology, Cardiovascular, and Infectious Diseases. This full-time, office-based position is designed for individuals looking to develop their careers in a fast-paced and collaborative environment, with a comprehensive training program provided for those without prior clinical research experience.

Responsibilities

  • Engage in clinical trial management on a day-to-day level.
  • Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy.
  • Compile and maintain project-specific status reports.
  • Interact with the Sponsor, study sites, and internal associates.
  • Provide oversight and quality control of our internal regulatory filing system.
  • Manage study supplies.
  • Create and maintain project timelines.
  • Coordinate project meetings and produce quality meeting minutes.

Requirements

  • Bachelor's degree in a health/life sciences field.
  • Prior experience as a Study Coordinator or within the pharmaceutical industry.
  • Excellent computer skills (word-processing, databases, Excel, Windows).
  • Strong organizational and communication skills.

Benefits

  • Medical insurance
  • Dental insurance
  • Vision insurance
  • 401(k) plan
  • Vacation policy
  • Sick days
  • Paid holidays
  • Work from home flexibility
  • Short-term disability
  • Long-term disability
  • Health savings accounts
  • Flexible savings accounts
  • Life and AD&D insurance
  • Pet insurance
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