or apply directly on Pulmovant's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 5 days Pulmovant's roles stay open a median of 13 days
- Reposted
- No
- Salary listed
- No 0% of Pulmovant's roles list one
- Ghost-job risk at Pulmovant
- low 0 stale, 0 reposted of 7 open
- Hiring momentum
- 7 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-28
Measured from postings appearing on and disappearing from Pulmovant's own greenhouse board since 2026-08-03. Full hiring picture for Pulmovant.
About this role
The Clinical Development Lead (MD) at Pulmovant will oversee the design and execution of clinical trials for mosliciguat, focusing on pulmonary hypertension associated with interstitial lung disease. Responsibilities include providing medical oversight, collaborating with cross-functional teams, and maintaining relationships with key opinion leaders and regulatory authorities. The role demands hands-on leadership in trial execution, protocol development, and data interpretation, particularly for the ongoing Phase 3 trial.
- benefits
- 1/5
- freshness
- 5/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Pulmovant as an employer.
What you need
- MD/DO degree or equivalent
- Minimum of 5 - 7 years experience conducting clinical research trials in the biopharmaceutical industry
- Hands on experience in protocol development and clinical trial monitoring
- Strong written and verbal communication skills
- Ability to work within and lead a cross-functional matrixed team
- Willingness to educate and mentor internal and external colleagues
Nice to have
- Board Certification or Board Eligibility in internal medicine with subspecialty training or experience in drug development in cardiopulmonary / respiratory medicine
- Experience with U.S. and European Health Authority interactions and submission of clinical regulatory documents
Worth weighing
- No salary listed
- Role involves significant responsibility in a clinical-stage biotechnology setting
- Requires strong leadership and communication skills in a dynamic environment
Summarised from Pulmovant's posting. Read the full original.
Listed by Pulmovant on their greenhouse job board, last confirmed open on 2026-09-28. PitchMeAI is not the employer.
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