Clinical Research Assistant
HelsinkiCompetitive0 applicants
About this role
About us
AIATELLA is a Helsinki-based medical AI company building software that measures blood vessels automatically from routine medical imaging. Our mission is simple: every vessel, every image, every body.
Responsibilities
- We are looking for a Clinical Research Assistant to support our clinical team across research, grant work and project management. This is a broad role in a small company: you will not be doing one thing repeatedly, and you will see how clinical evidence, regulatory submissions and funding fit together.
- You will work directly with our CEO and our Clinical Operations Manager, and you will be in regular contact with clinical investigators, hospital research teams and external collaborators.
- What you will do Support the day-to-day running of our multi-site clinical studies, including site communication, documentation and study tracking
- Help maintain study documentation and records to GCP standards, and support data entry and quality checks in our electronic data capture system
- Assist with ethics and regulatory submissions and the correspondence that follows them
- Contribute to grant applications and reporting: drafting, evidence gathering, budgets and deadline management
- Support the preparation of manuscripts, abstracts, posters and conference material
- Keep projects moving: agendas, minutes, action tracking, and chasing the things that need chasing
- Carry out literature searches and background research to support clinical, regulatory and commercial work
Requirements
- EssentialAt least one year of hands-on experience supporting a live clinical study: recruiting, data collection, monitoring, coordination or similar
- Working knowledge of GCP and the practical realities of running research at a clinica
About AIATELLA
AIATELLA is a Helsinki-based medical AI company building software that measures blood vessels automatically from routine medical imaging. Our mission is simple: every vessel, every image, every body. We are a small, hands-on team. Our software is developed under a quality management system aligned with ISO 13485 and ISO 14971, and involves FDA, EU MDR, and ANVISA bodies. Our clinical evidence programme runs across EMEA, LATAM and North America