or apply directly on Pulmovant's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 4 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 Senior Manager, Pharmacovigilance at Pulmovant will oversee safety surveillance and risk management for respiratory therapeutics, particularly focusing on the investigational candidate mosliciguat. Responsibilities include managing case processing, signal detection, and aggregate safety reporting while ensuring compliance with global regulations. The role requires collaboration with clinical development, regulatory affairs, and medical teams, and involves mentoring junior staff as the company scales towards commercialization.
- 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
- Bachelor's degree in life sciences, nursing, pharmacy, or related field
- Minimum of approximately 7+ years of pharmacovigilance/drug safety experience in the biotechnology or pharmaceutical industry
- Demonstrated experience with clinical trial safety surveillance and case management
- Working knowledge of global PV regulations and guidance (FDA, EMA, ICH E2 series, GVP modules)
- Experience authoring or contributing to DSURs, PSURs/PBRERs, and risk management plans
- Familiarity with safety database systems such as Oracle Argus Safety
Nice to have
- Advanced degree (PharmD, PhD, MSN, or MPH)
- Post-marketing pharmacovigilance and/or launch-readiness experience
- Experience supporting health authority inspections or internal/external audits
- Experience negotiating or managing Safety Data Exchange Agreements (SDEAs) and pharmacovigilance agreements (PVAs) with development or commercial partners
Worth weighing
- Role involves significant responsibility in a fast-paced environment, which may be challenging for some candidates
- No specific salary or benefits information provided
- Experience with Argus Safety is a key requirement, which may limit candidates without this specific background
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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