Virtual Career Event - Clinical Operations - South Korea

Medpace; United States; On-site; USD 50,000 - 70,000; Full time

Job summary

Medpace is hosting a Virtual Career Event for candidates with degrees in Life Science or related fields, focusing on opportunities in Clinical Operations. Attendees will learn about the company and available positions, with responsibilities including project coordination and collaboration on global study activities.

Benefits

Competitive total compensation and benefits package

Opportunities for internal growth

Qualifications

• Previous experience in the Clinical Trial industry is preferred.
• Fluency in the local language and excellent English skills.

Responsibilities

• Communicating and collaborating on global study activities.
• Ensuring timely delivery of recurrent tasks with high accuracy.
• Maintaining project-specific status reports within data management systems.

Skills

Communication

Collaboration

Attention to detail

Education

Bachelor's, Master's, or PhD in life sciences or a related field

Job description

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 discussions about potential job opportunities 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 Clinical Operations at the 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 event format will be provided if you are selected to attend. We're excited to speak with you!

Responsibilities

Depending on the position, responsibilities may include:

• Communicating and collaborating on global study activities;
• Ensuring timely delivery of recurrent tasks 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, Master's, or PhD in life sciences or a related field;
• Previous experience in the Clinical Trial industry is preferred;
• Fluency in the local language and excellent English skills.

Medpace Overview

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 a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across major areas including oncology, cardiology, metabolic diseases, endocrinology, central nervous system, antiviral, and anti-infective therapies. Headquartered in Cincinnati, Ohio, we employ over 5,000 people across more than 40 countries.

Why Medpace?

Joining Medpace means becoming part of a team dedicated to supporting the development of groundbreaking drugs and devices. Our employees give hope to those living with debilitating diseases. We offer a competitive total compensation and benefits package and opportunities for internal growth.

Awards:

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024
• Consistently awarded 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. If interested, you will be contacted for an RSVP. Responsibilities may include:

• Communicating and collaborating on global study activities;
• Ensuring timely delivery of recurrent tasks with high accuracy;
• Maintaining project-specific status reports within data management systems;
• Interacting with project teams, sponsors, study sites, and vendors;
• Coordinating meetings and producing minutes.