Project Coordinator III – Peripheral Vascular Health
Job in
6200, Maastricht, Limburg, Netherlands
Listed on 2026-09-25
Listing for:
Planet Pharma
Part Time
position Listed on 2026-09-25
Job specializations:
-
Healthcare
Clinical Research, Healthcare Compliance, Medical Science
Job Description & How to Apply Below
Join Our Team as a Project Coordinator III – Peripheral Vascular Health and Make a Difference in Patient Care
Are you passionate about advancing healthcare and coordinating impactful clinical initiatives? We’re seeking a dedicated Project Coordinator III to join our Peripheral Vascular Health Clinical Organization. In this vital role, you’ll provide essential support to clinical teams and studies, helping to drive innovations that improve patient outcomes worldwide. If you thrive in a dynamic environment and possess strong project management skills, this is your chance to contribute to life-changing therapies in a collaborative, inclusive setting.
What You’ll Bring to the Role:- At least 4 years of administrative or project coordination experience, ideally within clinical research or the medical device industry
- Exceptional verbal and written communication skills in English
- Demonstrated ability to manage multiple tasks with precision and attention to detail
- Strong proficiency with Microsoft Office Suite (Excel, PowerPoint, Word) and familiarity with project management tools and web-based applications
- Basic knowledge of GCP and regulatory guidelines for clinical trials
- Experience with clinical study documentation, systems, and compliance standards is advantageous
Skills and Experience:
- Bachelor’s or Associate degree preferred
- Over 5 years of experience in project coordination or administrative support within clinical settings
- Experience working with clinical trial systems such as Siebel CTMS and TMF platforms
- Knowledge of cardiovascular therapies and medical terminology
- Familiarity with process improvement methodologies and system support for clinical studies
Education and Experience:
- Bachelor’s degree or higher in life sciences, healthcare, or related fields
- Proven track record in clinical research or medical device product support, especially in cardiovascular therapies
- Experience working in a regulated environment with knowledge of GCP and FDA/ISO standards
- Location:
Maastricht, Netherlands (hybrid model requiring 2-3 days per week in-office) - Contract length: 12 months
- Full-time, 40 hours per week
- Immediate start preferred
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