Serve as clinical science lead on respiratory studies (asthma/COPD) in Phase 2/3.
Drive protocol development, data analysis, and regulatory documents for trials.
Lead late-stage trial design and execution in asthma and COPD.
Collaborate with cross-functional teams on trial design and execution.
Provide scientific input into CRFs, databases, and analysis plans.
Lead and mentor teams; ensure high standards of quality and rigor.

🎯 Requirements

PhD/PharmD/MD or equivalent in respiratory science.
9+ years in industry clinical development, late-stage respiratory trials.
Expertise in protocol design and regulatory documents (CSRs, IBs).
Strong knowledge of GCP and regulatory guidelines.
Ability to interpret clinical data with cross-functional partners.
Excellent communication, collaboration, and leadership skills.

🎁 Benefits

Annual bonus
Equity compensation
Competitive benefits package

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