• Job Description

  Req#: 11400

  Medpace is delighted to host a Virtual Career Event tailored to candidates with all levels of degree(s) in Life Science or related. This is a rare and exciting opportunity for individuals seeking an understanding in the Clinical Trials Industry! There will be introductory talks from various Clinical Operations departments and discuss what potential job opportunities are available now and in the future.

  Join us on 3 July 2025, Thursday from 2pm to 3.30pm (KST) to learn about Medpace and our available positions in the Clinical Operations in Medpace Korea Office.

  LOCATION: Virtual (Meeting link will be provided to selected candidates)

  DATE: 3 July 2025 (Time: 2pm - 3.30pm KST)

  APPLICATION CLOSE DATE: 28 June 2025

  What to Expect Next:

  A member of our recruitment team will review your qualifications. More details regarding the format of the event will be provided should you be selected to attend. We're excited to speak to you!

  
  Responsibilities
  
  

  Dependent on the position but may include;

  • Communicating and collaborating on global study activities;
  • Ensuring timely delivery of recurrent tasks, consistently, with a high degree of accuracy;
  • Compiling and maintaining project-specific status reports within department-specific data management systems;
  • Interacting with internal project teams, Sponsors, study sites, and third-party vendors;
  • Coordinating project meetings and producing quality minutes.

  
  Qualifications
  
  

  • Bachelor's degree, Masters or PhD in life science pr related field;
  • Previous experience in the Clinical Trial industry is welcome;
  • Fluency in local language and excellent English.

  
  Medpace Overview
  
  

  Medpace is a full-service clinical contract research organization (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

  
  Why Medpace?
  
  

  When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.

  Awards:

  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

  What to Expect Next:

  A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an RSVP.

  
  

  • Bachelor's degree, Masters or PhD in life science pr related field;
  • Previous experience in the Clinical Trial industry is welcome;
  • Fluency in local language and excellent English.

  
  

  Dependent on the position but may include;

  • Communicating and collaborating on global study activities;
  • Ensuring timely delivery of recurrent tasks, consistently, with a high degree of accuracy;
  • Compiling and maintaining project-specific status reports within department-specific data management systems;
  • Interacting with internal project teams, Sponsors, study sites, and third-party vendors;
  • Coordinating project meetings and producing quality minutes.

• About the company

  Medpace Holdings, Inc. is a midsize, clinical contract research organization based in Cincinnati, Ohio.

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