Clinical Trial Coordinator

PPD Europe

View: 109

Update day: 31-08-2023

Location: Brussels Brussels Capital

Category: R & D IT - Software


Position: Entry level

Job type: Contract

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Job content

We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD clinical research services - 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 clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality review of data and effective interaction with study sites, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants.

PPD clinical research services is currently looking for a Clinical Trial Coordinator to join our Clinical Operations 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.
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.
What We Offer
  • Learning and development programme, ensuring you reach your potential;
  • Extensive benefits package based around the health and well- being of our employees;
  • Competitive salary;
  • Flexible working culture with work- life balance and possibility for remote working;
  • Collaborative and friendly environment;
  • Global exposure and opportunity to work on international assignments.
Our 4i Values:

Integrity – Innovation – Intensity – Involvement

If you resonate with our 4i values above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, submit your application – we’d love to hear from you!

PPD clinical research services is now part of Thermo Fisher Scientific. As the world leader in serving science, our Mission is to enable our customers to make the world healthier, cleaner and safer. We are excited about the opportunities this combination brings to enhance our comprehensive end-to-end offering, enabling customers to move rapidly from scientific idea to approved medicine.
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Deadline: 15-10-2023

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