Respiratory Clinical Scientist Lead

Expedition Therapeutics Inc.; San Francisco (CA); On-site; USD 180,000 - 240,000; Full time

Job summary

Expedition Therapeutics Inc. seeks an Associate Director/Director, Clinical Scientist to lead clinical development studies in COPD, Bronchiectasis, and Asthma.

You will partner with Clinical Operations, Biostatistics, Regulatory Affairs, and CMC to design, execute, and interpret trials that support global development and regulatory approval. The role requires hands-on protocol development, trial execution, and translating complex clinical data into actionable insights for cross-functional and

Qualifications

• Advanced degree or equivalent with substantial clinical development experience.
• Associate Director: 4+ years; Director: 5-7+ years of clinical research/clinical development experience.
• Experience in respiratory or related inflammatory therapeutic areas preferred.
• Experience authoring/reviewing protocols, ICFs, and CSR.
• Strong communication and collaboration with CROs and sites.
• Proven ability to operate strategically and execute in a fast-paced environment.

Responsibilities

• Serve as clinical science lead/co-lead for studies (Phase 1b/2/3) evaluating COPD, Bronchiectasis, and Asthma.
• Contribute to development plans, study protocols, and amendments with leadership.
• Authorship/review of protocols, ICFs, CRFs, SAPs, and study reports.
• Serve as contact for CROs, investigators, and clinical sites.
• Review and interpret trial data; support DMC, safety monitoring, and data cleaning.

Skills

Clinical trial leadership

Protocol development

Data interpretation

Regulatory liaison

Cross-functional collaboration

Scientific communication

Education

PhD in life sciences

MD/DO/PharmD equivalent

Tools

ICH-GCP knowledge

CRO/vendor management

Job description

Expedition Therapeutics Inc. seeks an Associate Director/Director, Clinical Scientist to lead clinical development studies in COPD, Bronchiectasis, and Asthma.

You will partner with Clinical Operations, Biostatistics, Regulatory Affairs, and CMC to design, execute, and interpret trials that support global development and regulatory approval. The role requires hands-on protocol development, trial execution, and translating complex clinical data into actionable insights for cross-functional and