Clinical Development Lead (MD), Pulmovant
Pulmovant · United States · US
Clinical Research
Remote
physician
Demand85
Career growth80
Healthcare fit78
Remote potential20
5-year outlook
Senior Director-level biopharma clinical development roles typically offer strong total compensation with potential for VP/clinical program leadership; exact figures depend on company stage, location, and equity.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-10-02
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- physician
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth applying for physician-scientists with prior clinical trial/industry experience who want a senior biopharma clinical development leadership role. Not practical for early-career clinicians or those without pharma/Phase 3 experience.
Who should apply
MD/physician-scientists with pulmonary, critical care, or ILD experience; prior pharma/biotech clinical development or medical monitoring experience; track record in Phase 3 trial design/execution, KOL engagement, and regulatory interactions.
CV angle
Frame MD and board certification, then quantify clinical trial leadership: protocol design, Phase 3 execution, site activation, recruitment, data review, safety reporting, GCP compliance, regulatory submissions, and KOL/Health Authority interactions. Highlight pulmonary hypertension/ILD therapeutic expertise and cross-functional team leadership.
Skills to highlight
- Clinical trial design
- Phase 3 trial execution
- Protocol development
- GCP compliance
- Regulatory interactions
- KOL engagement
- Medical monitoring
- Data interpretation
- Cross-functional leadership
- Pulmonary hypertension/ILD
Role summary
Senior physician leader at Pulmovant/Roivant responsible for clinical development of mosliciguat in PH-ILD, including Phase 3 trial design, execution, medical oversight, and regulatory/KOL strategy.
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