Respiratory- Subject Matter Expert

About the Role We’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 boarded‑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 You We’d like to hear from you if… 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. meaningful exposure to clinical research – whether as a principal investigator, sub‑investigator, sponsor‑side medical monitor, scientific advisor, or contributor to protocol development. translate clinical reality into research design – flagging recruitment challenges, refining endpoints, and pressure‑testing study assumptions before they become problems. comfortable advising across respiratory indications spanning asthma, COPD, idiopathic pulmonary fibrosis (IPF), interstitial lung disease, bronchiectasis, cystic fibrosis, pulmonary hypertension, sleep‑disordered breathing, respiratory infections, or other pulmonary sub‑specialties. comfortable speaking to spirometry, lung function endpoints, and respiratory biomarkers – and can advise on what makes them robust (or fragile) in a trial setting. strong communication skills and can hold your own in a room with sponsors, regulators, and cross‑functional clinical teams. responsive and reliable , and able to turn around expert input on tight timelines when trials demand it. comfortable working independently as a 1099 contractor , managing your own schedule and engagements alongside your wider clinical commitments. excited to share your expertise across multiple studies and help shape best practice in respiratory research. embody Lindus Health values: Be Transparent, High Agency, and Benefit Patients. What You’ll Focus On Protocol & Study Design Input : Provide expert review of respiratory trial protocols, advising on inclusion/exclusion criteria, endpoints (FEV1, exacerbation rates, PROs), safety monitoring, and procedural feasibility from a practising clinician’s perspective. Feasibility & Site Strategy : Sense‑check recruitment assumptions, identify practical barriers to enrolment, and advise on site and investigator selection within the respiratory community. Sponsor & Business Development Support : Lend clinical and scientific credibility to prospect conversations, helping the Commercial team articulate Lindus’s value to respiratory‑focused sponsors. Participate in feasibility calls and scientific discussions where SME input strengthens our position. Medical & Safety Oversight : Offer ad‑hoc clinical guidance on safety signals, adverse events, and patient safety considerations across active respiratory trials, working alongside our internal medical team. Investigator & KOL Engagement : Act as a peer voice to investigators and external KOLs where helpful, supporting Lindus’s reputation as a credible scientific partner in respiratory medicine. Best Practice Contribution : Share insights from clinical practice and the wider pulmonology community to help shape SOPs, training materials, and study management approaches for respiratory trials. What We Offer Competitive 1099 rate tied to the engagement, with flexibility to focus on the trials and topics where your expertise adds the most value. A flexible, ad‑hoc engagement model designed to fit around your clinical practice – no minimum hours, no commitment to a fixed schedule. Direct exposure to a high‑quality portfolio of clinical trials and innovative sponsors working in the respiratory and pulmonary space. The chance to shape how respiratory research is run , partnering with a team that’s genuinely changing healthcare for the better. A collaborative, mission‑driven culture where your clinical expertise is genuinely valued and acted on. Hiring Process Initial conversation with Cam, our ClinOps Talent Partner (20 mins) – Get to know each other, walk through the contractor model, and answer any questions about Lindus. Clinical & scientific conversation with our Medical leadership (30 mins) – Discuss your respiratory background and clinical research experience, and explore how you’d add value to our studies. We will only contact you from lindushealth.com email addresses. Please check the spelling of emails which appear to come from Lindus carefully before responding. We will never ask for your financial information over email. We are an equal opportunity employer committed to building a diverse and inclusive workforce. We evaluate all candidates based solely on their skills, experience, and qualifications relevant to the role. We do not discriminate on the basis of race, ethnicity, religion, gender, gender identity, sexual orientation, age, disability, veteran status, or any other legally protected status. #J-18808-Ljbffr