Clinical Trial Manager

You will own the operational execution of Noah Labs' US and EU clinical programs — the FDA pivotal trial (15+ sites, De Novo submission) and a randomized pragmatic trial embedded in routine care, as well as oversight of European MDR investigations. You're building the clinical operations function itself, managing sites directly, coordinating academic partners and specialist vendors, and helping grow the clinical team as the company scales toward clearance.

What you'll do

• Lead trial start-up including site selection, agreements, and budgets, IRB submissions, site initiation and training
• Drive enrollment and protocol adherence across sites in close partnership with investigators and site coordinators
• Own the monitoring strategy and personally conduct monitoring visits, both remote and on-site, in addition to managing any contract monitors
• Own study budgets, timelines and risk registers, reporting directly to the Chief Medical Officer
• Run the operational backbone: eTMF, EDC, data cleaning, and protocol deviations
• Ensure audit and inspection readiness (FDA BIMO, IRB) and maintain sponsor SOPs
• Support the European investigations and regulatory compliance (ISO 14155, MDR)
• Author and maintain SOPs and work instructions for clinical operations, monitoring, and data management

What you'll need

• Degree in life sciences, nursing, medicine, biomedical engineering or a related field
• 5+ years in clinical research, including 3+ years in US FDA-regulated devices
• Familiarity with SaMD clinical trials
• Hands-on experience with the full IRB submission lifecycle: preparing and submitting packages, then amending documents like the CIP and ICF as the protocol changes
• Hands-on experience taking a US multicenter trial from start-up through enrollment and closing, on the sponsor side and without a full-service CRO
• Working knowledge of 21 CFR Parts 812, 50, 56 and 11, ICH-GCP, ISO 14155 and HIPAA; practical experience with EDC and eTMF systems
• Uncompromising on patient safety, data integrity and inspection readiness
• Authorized to travel to the US without Visa restrictions (e.g. ESTA-eligible)

Nice to have

• Cardiology or heart failure trials; pragmatic or health-system-embedded trials
• App-based or remote monitoring studies (patient onboarding, adherence, technical support)
• Contribution to a De Novo, 510(k) or PMA clinical evidence package
• Advanced academic degree (e.g. MSc)

What they offer

• Competitive pay plus meaningful equity
• Bring a first-in-class digital biomarker through FDA clearance and into routine care
• Dynamic startup with exceptional talent from Harvard, TUM, Meta and Stanford
• Based at Berlin headquarters with regular visits to US sites and flexibility to work remotely
• Direct exposure to leading US cardiology centers and the FDA Breakthrough Devices process
• Access to Urban Sports Club