Will you be the new Clinical Trial Administrator?
Help build groundbreaking therapies for neurodegenerative diseases.
At our clients organization, they believe that patients with diseases like ALS and Huntington’s can no longer wait. They combine the power of antibodies with innovative AAV delivery to provide long-lasting solutions for diseases that currently have no treatment.
Since starting in 2020 at the Amsterdam Science Park, they have grown rapidly. With a strong financial foundation, they are now a fully integrated company ready for the next step: bringing their vectorized antibody therapies into the clinic.
Your Role in the Team
As a Clinical Trial Administrator (CTA), you will become part of their passionate Clinical Team. They are responsible for designing and executing complex, cutting-edge clinical trials. You are the "spider in the web" who ensures everything runs flawlessly behind the scenes, allowing the team to focus on saving lives.
What will you do?
- TMF Ownership: You ensure a perfectly structured and "inspection-ready" Trial Master File. You oversee filing and ensure everything is accurate and complete.
- Collaboration: You interface continuously with internal teams, research sites, and external partners to ensure documentation is completed on time and in compliance with regulations.
- Operational Support: Whether it’s preparing meetings, maintaining registries (such as ClinicalTrials.gov), or reviewing documents, you ensure the engine keeps running.
- Quality & Compliance: You play a key role in inspection readiness and provide support for SOPs and quality assurance.
- Financial Overview: You assist in tracking budgets and the financial processing of our studies.
Who are they looking for?
We aren't looking for a "box-ticker," but rather an organizational talent who gains energy from a dynamic environment where no two days are the same.
Your Profile:
- You communicate fluently in English (both verbal and written).
- You are a star at planning and multitasking; deadlines do not intimidate you.
- You enjoy working independently and with discipline, whether at our Amsterdam office or from home.
- You have a sharp eye for detail and are only satisfied when everything is processed accurately.
- You are proficient with MS Office (Word, Excel, Teams, SharePoint).
- Your Natural Strength: You are a true team player with a strong sense of responsibility. When a problem arises, you roll up your sleeves and solve it with a healthy "sense of urgency." You enjoy diving into the scientific context of our work and stay up-to-date with the latest GCP and regulatory standards.
Why choose this employer?
You will work in an ambitious, international team at the Amsterdam Science Park. Lines of communication are short, the impact is huge, and the atmosphere is driven yet informal. We offer you the chance to truly make a difference for patients worldwide.