Job Details
Posted 22 September, 2026
Job Id: 631127
Project Coordinator III – Peripheral Vascular Health
Job Description
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
Nice to Have 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
Preferred 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
Additional Requirements:
- 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
Take the next step in your career to impact millions of lives through innovative therapies–apply now and become part of a team committed to changing healthcare worldwide!
Equal Opportunity Employer
We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert
Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
