Data Coordinator - CRO (Leuven, Entry-Level) at Medpace, Inc.

Leuven, Flemish Brabant, Belgium -

Full Time

Start Date

Immediate

Expiry Date

06 Jul, 26

Salary

0.0

Posted On

07 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Data management, Clinical data analysis, Database design validation, Data conflict resolution, Data reconciliation, Documentation management, Microsoft Excel, Microsoft Word, English communication, Attention to detail, Clinical research, Metrics reporting

Industry

Pharmaceutical Manufacturing

Description

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Data Coordinator to join our Data Management team in Leuven, Belgium. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. By studying clinical data, these professionals ensure the accuracy of data that is reported from clinical studies. At Medpace, Data Coordinators go through an extensive onboarding and training process, which prepares them to become experts in their field. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Participate as part of a team on various project(s) Validate an entry database design Report metrics and data trends on project(s) Identify data conflicts and issues on project(s) Collaborate with research sites globally to resolve data conflicts Reconcile data from multiple sources Create and update study documentation on project(s) Qualifications Bachelor's degree in Life Sciences or Mathematics Strong attention to detail Excellent working knowledge of Microsoft Excel and Word Solid oral and written English Language communication skills We kindly ask to send applications in 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? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives 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 Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Responsibilities

The Data Coordinator will validate database designs, report on data trends, and identify data conflicts within clinical studies. They will also collaborate with global research sites to resolve discrepancies and maintain accurate study documentation.