Serve as clinical science lead on respiratory studies (asthma/COPD)
Act as a key scientific contributor to late-stage protocols and regulatory submissions
Design and develop clinical trial protocols and docs with the clinical development lead
Drive clinical study plans, data review plans, and regulatory documents (IBs/CSRs)
Interpret clinical data in collaboration with cross-functional colleagues and external partners
Participate in data review and medical monitoring activities

🎯 Requirements

Advanced degree (PhD/PharmD/MD) required; respiratory background preferred
9+ years in clinical development with direct late-stage respiratory studies
Proven ability to lead clinical science strategy and execution in late-stage trials
Strong knowledge of clinical research methodologies, regulatory guidelines, and GCP
Experience authoring protocols, CSRs, and regulatory documents

🎁 Benefits

Annual bonus eligibility
Equity compensation
Competitive benefits package

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