Location: Flexible within Europe (remote work possible)
Position type: Full-time
Start date: As soon as possible
VERIGRAFT is a pioneering biotechnology company developing personalized tissue therapies for patients with serious and currently untreatable conditions. Our lead product, P-TEV, is currently in early clinical development for the treatment of Chronic Venous Insufficiency (CVI).
As we prepare for Phase II clinical trials in Europe and the United States, we are expanding our team and looking for a highly motivated Clinical Trial Coordinator to set up and progress our upcoming clinical trials at the highest possible speed. You should be able to face the challenges of setting up and performing clinical trials in this new field and should personally push a variety of stakeholders and find the leanest way to initiate and execute our clinical trial program.
Your role
As Clinical Trial Coordinator, you will be responsible for planning, coordinating, and overseeing the execution of our upcoming multi-center Phase II clinical trials. You will play a central role in ensuring that studies are conducted efficiently, ethically, and in compliance with all regulatory requirements.
Main responsibilities
- Responsibility for the execution and coordination of clinical trial activities across multiple sites in Europe and the U.S.
- Serve as the main point of contact for clinical sites, investigators and CROs
- Site selection and assessment, and contract negotiations with hospitals/ investigators
- Drive trial progress and timelines, ensuring proper documentation and reporting
- Support regulatory submissions and interactions with ethics committees and authorities
- Contribute to the development and review of study documents
- Work closely with the Clinical RA/QA Manager to align clinical trials with operational plans, reporting to the CTO.
- Together with the Clinical QA/RA Manager, ensure inspection readiness according to ICH GCP E6 (Sponsor Oversight)
Qualifications and experience
- Bachelor’s or master’s degree in life sciences, nursing, pharmacy, or related field
- Proven experience in coordinating clinical trials, ideally within Phase II or later-stage studies
- Strong knowledge of the legal requirements for clinical trial execution in Europe and the U.S.
- Hands-on experience of working according to ICH GCP E6
- Ability to manage multiple stakeholders and adapt to changing circumstances
- Fluent in English (spoken and written); other languages are a plus
- Willingness to travel extensively across Europe and the U.S. as needed
Personal qualities
We are looking for someone who is:
- Proactive, self-driven, and solution-oriented
- Driven to personally make operational plans a reality and willing to do the necessary footwork.
- Skilled in building strong working relationships across teams and cultures
- A team player with a positive and flexible mindset
What we offer
- A unique opportunity to work at the forefront of regenerative medicine
- A collaborative and dynamic environment within a purpose-driven team
- Flexibility in work location and schedule
- Competitive performance driven compensation and benefits package
- The chance to contribute to clinical developments with the potential to transform lives
Want to join us?
Please send your CV and personal letter to jobs@verigraft.com. For more information about VERIGRAFT and our technology, visit www.verigraft.com