or apply directly on Pulmovant's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 22 days Pulmovant's roles stay open a median of 15 days
- Reposted
- No
- Salary listed
- No 0% of Pulmovant's roles list one
- Ghost-job risk at Pulmovant
- low 0 stale, 0 reposted of 4 open
- Hiring momentum
- 4 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
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 Senior Manager of Regulatory Affairs at Pulmovant will be responsible for executing global regulatory strategies and ensuring compliance throughout the clinical development process. This role involves representing Regulatory Affairs in project meetings, preparing regulatory submissions, liaising with health authorities, and developing internal policies. The position requires collaboration with cross-functional teams and external parties to support clinical trials and product registration.
- benefits
- 1/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 4/5
- 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
- BS degree in a scientific field with 7 years of experience in regulatory affairs, or MS degree with 5 years, or PhD/PharmD with 3 years
- Experience working with the FDA
- Excellent communication and interpersonal skills
- Ability to multi-task in a fast-paced environment
- Highly proficient using Microsoft Office applications
- Strong financial business acumen and analytical skills
Nice to have
- Experience with EU, Japan, and other global health authorities
- Experience interacting with the FDA Division of Cardiology and Nephrology
- Experience with pulmonary hypertension and other pulmonary diseases
- Regulatory Affairs Certification (RAC) in drugs and/or devices
- Experience with global clinical trials using a CRO
Worth weighing
- Remote position may require coordination across different time zones
- Travel up to 10% may be required
- No specific salary or benefits information provided
Summarised from Pulmovant's posting. Read the full original.
Listed by Pulmovant on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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