Clinical Trial Coordinator - Brussels

☞ PPD

見る: 140

更新日: 26-11-2025

場所: Brussels Brussels Capital

カテゴリー: R & D IT-ソフトウェア

業界: Biotechnology Pharmaceuticals Research

ジョブタイプ: Full-time

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仕事内容

Job Description

We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients.  

Our global Clinical Monitoring department consists of colleagues with institutional knowledge, in-depth therapeutic experience, and robust operational tools. Together, we help clients define and develop clinical programmes, minimise delays and execute high-quality, cost-efficient clinical studies.

PPD is currently looking for a Clinical Trial Coordinator to join our clinical team in Brussels. We will offer you a positive and supportive working environment within one of the most engaged teams in the industry. We will provide you with meaningful and challenging work and the opportunity to acquire valuable personal and professional skills, through our best in class training and development.

As a Clinical Trial Coordinator you will provide technical support to the project team. Will coordinate non-clinical responsibilities of project administration as applicable to the client contract under the direction of the assigned Clinical Manager or Sr. Clinical Manager.

Responsibilities Include

, But Are Not Limited To
  • Reviews regulatory documents for proper content
  • Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools
  • Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments
  • Assists with the identification of potential investigators and development/distribution of initial protocol packets
  • Creates meeting agendas and minutes
  • Coordinates team conference calls and distribution of meeting minutes
Job Qualification

Education And Experience
  • Excellent English, French and Dutch language skills
  • Working skills across all of the Microsoft packages
  • Ability to effectively analyse project specific data/systems to ensure accuracy and efficiency
  • Strong interpersonal skills and high attention for detail, with proven ability to handle multiple tasks efficiently and effectively
  • Good communication skills
  • Ability to handle multiple tasks effectively
  • Excellent organisational skills will be necessary, along with a self-motivated and positive attitude
  • Some previous administration experience, preferably within clinical research, although this is not essential.
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD truly value a work-life balance. We’ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel.

PPD Defining Principles
  • We have a strong will to win - We earn our customer’s trust - We are gamechangers - We do the right thing - We are one PPD –
If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, then please submit your application – we’d love to hear from you.

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締切: 10-01-2026

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