Job Description
📋 Description Lead clinical science for respiratory studies (asthma/COPD) Oversee day-to-day study execution per protocol and timelines Design trial protocols and key documents (SP, CSR, CRF, SAP) Contribute to regulatory documents (IBs, CSRs, briefing books) Monitor safety and data quality with cross-functional teams Manage site selection, initiation, and investigator inquiries 🎯 Requirements Advanced degree (PhD, PharmD, MD, MS, PMP) and 9+ years in clinical development, including late-stage respiratory Strong knowledge of clinical research methods, regulatory guidelines, and GCP Demonstrated ability to lead clinical science strategy and execution in late-stage trials Excellent analytical, communication, and cross-functional collaboration skills Prior experience authoring clinical protocols, CSRs, and regulatory documents 🎁 Benefits Remote work option with occasional travel to HQ
