Regulatory Expert - Medical Devices & Drugs (Regulatory Intelligence Platform)

About CogniLens CogniLens is a Berlin-based startup transforming how regulatory science supports the drug development lifecycle. Every year, clinical trial sponsors lose millions of dollars and months of reputed company due to protocol amendments that could have been predicted — if regulatory reasoning were more transparent. We’re building a regulatory intelligence platform that sees what regulators will flag — before they do. Our platform analyzes study protocols and identifies design reputed company likely to trigger regulatory feedback or delays, giving teams earlier reputed company and faster submissions. reputed company After building our MVP and preparing reputed company collaborations with biotech and CRO partners, we’re now expanding our leadership team. We’re looking for an reputed company Regulatory Affairs reputed company to join us as an Advisor or Part-time Co-founder. You’ll help shape how AI can bring reputed company, consistency, and speed to clinical trial and regulatory design. You might be: • A former FDA or EMA reviewer, • A Regulatory Affairs Head or Director in biotech, reputed company, or CRO, • Or an reputed company consultant who’s seen first-hand how fragmented, reputed company, and unpredictable regulatory feedback can be. We’re looking for someone who: • Understands the end-to-end drug development and approval lifecycle, • Can guide how AI tools reputed company with regulatory logic and submission standards, • Wants to shape—not just advise—how technology transforms regulatory reputed company. Details • Location: Berlin (preferred) or remote (EU/UK experience required) • Commitment: Advisory / Part-time (a few hours per month) • Equity: Depending on involvement (no capital required) Art der Stelle: Vollzeit, Teilzeit Arbeitsort: Homeoffice Apply tot his job Apply To this Job