Project Coordinator (CRO)

☞ Medpace

看过: 170

更新日: 16-11-2025

位置: Leuven Flemish Brabant

类别: 其他

行业: Pharmaceutical Manufacturing

水平: Entry level

工作类型: Full-time

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工作内容

Job Summary

Our clinical activities are growing rapidly in Belgium, and we are currently seeking a full-time Project Coordinator to join our Clinical Operations team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. 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.

As a paid, full-time project coordinator you will have the opportunity to work within Clinical Trial Management, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with Clinical Trial Managers, you will gain valuable hands on experience to enable you to develop a career in clinical research.

Responsibilities
  • Provide day-to-day departmental/project support activities, such as maintenance of project-related files and faxing documents to sites;
  • Coordinate and provide minutes for department/project meetings or conference calls;
  • Conduct quality control of documents;
  • Maintain spreadsheets and compile reports; and
  • Perform other tasks as needed.

Qualifications
  • Master or/and PhD degree is required (preferably in a Life Sciences field);
  • Some experience in an office setting is preferred;
  • Excellent organizational and prioritization skills;
  • Knowledge of Microsoft Office;
  • Great attention to detail and excellent oral and written communication skills; and
  • Preferred: Dutch & French language skills and fluency spoken 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?

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:
  • Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
  • Recognized by Forbes as one of America’s Best Mid-size Companies in 2021
  • Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
  • 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 interview.

EO/AA Employer M/F/Disability/Vets
  • WARNING: Please beware of phishing scams that offer opportunities with Medpace in exchange for sending money. These scammers pose as legitimate employees from actual companies. Please be advised that a Medpace employee will never ask you for a credit card, send you a check, or ask you for any type of payment as part of consideration for a role with our company. All of our careers require that you first complete an online application and go through some sort of interview process.
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最后期限: 31-12-2025

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