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Clinical Trial Coordinator

2 months ago

Irving Texas, United States Medpace, Inc. Full time
Job Summary:

Medpace, Inc. is seeking a highly organized and detail-oriented Clinical Trial Intern to join our Clinical Operations team in a full or part-time, office-based capacity. This internship will provide valuable hands-on training and support for various clinical trial management projects.

Key Responsibilities:
  • Provide day-to-day project support activities, including maintenance of project-related files and correspondence with study teams.
  • Perform administrative duties in accordance with company policies and procedures.
  • Coordinate and schedule meetings, provide meeting minutes, and maintain databases/project specific status reports.
  • Support filing and quality control reviews of our internal regulatory filing system.
  • Manage study supplies and perform other administrative tasks as needed.
Requirements:
  • Working towards a Bachelor's degree in a Life Science field.
  • Excellent organizational, communication, and prioritization skills.
  • Knowledge of Microsoft Office.
  • Availability to work a minimum of 20 hours per week in our office for 1-2 semesters.
About Medpace:

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.

Why Medpace?

At Medpace, we value our employees and offer a range of benefits, including hybrid work-from-home options, competitive PTO packages, flexible work hours, and a comprehensive compensation and benefits package. We are committed to providing a supportive and inclusive work environment that fosters professional growth and development.