Job Description
📋 Description Oversee late-stage asthma/COPD trials for safety, protocol compliance, and data integrity Act as primary medical contact for sites, investigators, and CROs; review eligibility Member of Clinical Development, Safety Management, and Study Execution teams Contribute to core clinical/regulatory documents (IB, ICF, RFI, protocols, DSUR) Support oversight committees (DSMB, endpoint adjudication); collaborate with Clinical Ops, Regulatory, Biostatistics, Pharmacovigilance Interpret trial data and contribute to study reports and regulatory filings 🎯 Requirements MD with board certification in Pulmonology or Allergy & Immunology preferred 8+ years clinical development experience in biopharma Extensive expertise in asthma and respiratory trial design, oversight, execution Strong cross-functional leadership and communication skills MD required; additional scientific training (fellowship/MPH) a plus Nice to have: experience in large pharma/biotech; familiarity with FDA/EMA; prior BLA/MAA submissions 🎁 Benefits Annual bonus Equity compensation Competitive benefits package
