Clinical Scientist Intern
Core
Intern supporting the development of Clinical Evaluation Reports (CER) and regulatory documents for EU CE Mark applications, including literature reviews and clinical data summaries.
Role type
Intern, clinical scientist (medical writing)
Builds
Clinical Evaluation Reports (CER) and regulatory documentation for EU CE Mark applications
Domain
Medical devices / Robotic surgery / Regulatory affairs
Required skills
Medical writing, Clinical literature review, Regulatory document authoring, Critical appraisal of scientific literature, GCP compliance, Document formatting and proofreading
Preferred skills
Academic research experience, Scientific writing, Analytical thinking, Cross-functional collaboration, Self-education in surgical specialties
Technologies
GCP, SOPs, Clinical Study Reports, Protocols, Conference abstracts, Peer-reviewed publications