Beschreibung

As the clinical authority for diabetes technologies, you will lead product evaluations and risk assessments while building strategic partnerships to drive the adoption of life-changing medical devices.

Anforderungen

• •Medical Degree or PhD with clinical evaluation experience
• •Experience in Diabetes or related field
• •Experience in pharma, medical device, or biotech
• •Understanding of Diabetes technical and medical state-of-the-art
• •Understanding of CGM business and technical state-of-the-art
• •Experience managing relationships with Diabetes experts
• •Understanding of clinical trial design and pharmacovigilance
• •Experience as Study Safety Officer
• •Strategic mindset for complex scientific concepts
• •Excellent communication, presentation, and interpersonal skills
• •Team player
• •Fluency in English and proficiency in German

Aufgaben

• •Lead clinical evaluation efforts for diabetes care devices
• •Author clinical evaluation reports and medical risk assessments
• •Provide medical input for safety and regulatory documents
• •Identify data gaps and lead data generation activities
• •Design and oversee post-market clinical follow-up plans
• •Act as study safety officer for clinical trials
• •Develop strategic relationships with clinicians and research institutions
• •Drive knowledge exchange regarding scientific advancements
• •Collaborate with clinical operations and regulatory affairs teams
• •Support interactions with health authorities and notified bodies
• •Ensure all medical activities meet ethical and regulatory standards

Tools & Technologien

Benefits