Respiratory- Subject Matter Expert

Respiratory- Subject Matter Expert LocationUSEmployment TypeFull timeLocation TypeRemoteDepartmentMedical Operations🍊Our missionGreat science regularly stalls in the clinic, not because the science is wrong, but because the company behind it lacks the capital, infrastructure, or focus to take it all the way through. Today’s clinical-stage biopharma model is broken, and as a result promising treatments never reach patients.Our mission is to fix this: we’re building the next generation of biopharma by in-licensing clinical-stage therapeutic assets and developing them through Lindus Health’s integrated, technology-first clinical trial infrastructure. We’re a new initiative, but we’re building on a proven foundation - the same infrastructure that has delivered 82% of Lindus Health’s sponsor trials on or ahead of timeline, across 40+ completed trials across the US and Europe.We’re in-licensing 5-7 clinical-stage, typically Phase-2-ready assets, funded directly from Lindus Health’s balance sheet. We’re targeting deal close on our first assets through 2026, with first trials launching in H1 2027.About the RoleWe’re building out our network of Clinical Subject Matter Experts and are looking for a board-certified respiratory physician (pulmonologist) to partner with us on a 1099 contract basis. You’ll act as a trusted clinical advisor across the lifecycle of our respiratory trials - from protocol design and feasibility through to study delivery, safety oversight, and sponsor engagement.This is an ad-hoc, as-needed engagement. You’ll be called in when our teams need a board-certified pulmonologist’s perspective: helping us design protocols that work in real-world respiratory practice, sense-checking inclusion/exclusion criteria, advising on patient safety, and lending scientific credibility to conversations with sponsors and investigators.You’ll partner closely with our Clinical Operations, Medical, and Business Development teams, while retaining the flexibility of a contractor model. This is a fully remote engagement open to respiratory physicians licensed and practising in the United States.About YouWe’d like to hear from you if…You’re a board-certified pulmonologist / respiratory physician with an active US medical licence and a track record of clinical practice in pulmonary and/or critical care medicine.You bring meaningful exposure to clinical research - whether as a principal investigator, sub-investigator, sponsor-side medical monitor, scientific advisor, or contributor to protocol development.You can translate clinical reality into research design - flagging recruitment challenges, refining endpoints, and pressure-testing study assumptions before they become problems.You’re comfortable advising across respiratory indications spanning asthma, COPD, idiopathic pulmonary fibrosis (IPF) and interstitial lung disease, bronchiectasis, cystic fibrosis, pulmonary hypertension, sleep-disordered breathing, respiratory infections, or other pulmonary sub-specialties.You’re comfortable speaking to spirometry, lung function endpoints, and respiratory biomarkers - and can advise on what makes them robust (or fragile) in a trial setting.You bring strong communication skills and can hold your own in a room with sponsors, regulators, and cross-functional clinical teams.You’re responsive and reliable, and able to turn around expert input on tight timelines when trials demand it.You’re comfortable working independently as a 1099 contractor, managing your own schedule and engagements alongside your wider clinical commitments.You’re excited to share your expertise across multiple studies and help shape best practice in respiratory research.You embody Lindus Health values: Be Transparent, High Agency, and Benefit Patients.What You’ll Focus OnProtocol & Study Design Input: Provide expert review of respiratory trial protocols, advising on inclusion/exclusion criteria, endpoints (FEV1, exacerbation rates, PROs), safety monitoring, and procedural...