Clinical Research Assistant

Your position

• Coordinate multi-site clinical research studies, including patient scheduling, data collection, and communication with collaborating centers
• Manage regulatory documentation: ethics submissions, amendments, and study master files
• Perform structured annotation and grading of retinal images (OCT, fundus photography, adaptive optics) following standardized protocols
• Serve as the primary liaison for external collaborators and study partners, ensuring timely and professional communication
• Assist with clinical trial preparation, including protocol development, case report form design, and site initiation support
• Maintain and curate research databases, ensuring data integrity and compliance with Good Clinical Practice (GCP)

Your profile

Minimum qualifications:

• At least BSc in biomedical sciences, optometry, orthoptics, biomedical engineering, life sciences, or a related field
• Excellent organizational skills and attention to detail
• Strong written and spoken communication in English and German
• Ability to work independently and manage multiple parallel projects
• Interest in ophthalmology, retinal diseases, or translational clinical research

Preferred qualifications:

• Prior experience in clinical study coordination, CRA roles, or GCP-regulated research environments
• Familiarity with ophthalmic imaging modalities (OCT, visual fields, fundus photography) or clinical grading systems
• Experience with research databases, REDCap, or electronic data capture systems
• Background in image annotation or structured data labeling for research or machine learning applications