Responsibilities

• Provide day-to-day medical oversight for late-stage clinical trials in asthma and/or COPD
• Ensure patient safety, protocol compliance, data integrity, and inspection readiness
• Serve as primary medical contact for clinical sites, investigators, and CROs
• Perform subject eligibility review, ongoing data reviews, and manage study queries
• Contribute as an author and reviewer for core clinical and regulatory documents (IB, ICF, RFI, study protocols, DSUR)
• Support study oversight committees including DSMB and endpoint adjudication committees
• Collaborate cross-functionally with Clinical Operations, Regulatory, Biostatistics, and Pharmacovigilance
• Interpret clinical trial data for study reports, regulatory filings, and publications

Requirements

• MD degree required
• 8+ years of clinical development experience in the biopharma industry
• Extensive expertise ...