Medpace - Cincinnati, OH

posted about 2 months ago

Full-time - Entry Level
Remote - Cincinnati, OH
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, Infectious Disease, and more. This full-time, office-based position is designed for individuals looking to thrive in a fast-paced, collaborative environment, with a comprehensive training program available for those new to clinical research.

Responsibilities

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

Requirements

  • Minimum of a Bachelor's Degree in a Life Sciences field.
  • Excellent computer, organizational, and time management skills.
  • Research experience preferred.

Benefits

  • Hybrid work-from-home options (dependent upon position and level)
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Flexible work schedule
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs
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