or apply directly on Parabilis Medicines's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 29 days Parabilis Medicines's roles stay open a median of 35 days
- Reposted
- No
- Salary listed
- Yes 100% of Parabilis Medicines's roles list one
- Ghost-job risk at Parabilis Medicines
- high 9 stale, 0 reposted of 19 open
- Hiring momentum
- 24 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 Parabilis Medicines's own greenhouse board since 2026-08-03. Full hiring picture for Parabilis Medicines.
About this role
The Senior Director, Safety Scientist at Parabilis Medicines will lead safety surveillance and risk management for clinical development programs. This role involves conducting signal detection, authoring safety documents, and collaborating with various teams to assess the benefit-risk profile of investigational products. The position requires strong expertise in pharmacovigilance and the ability to influence decisions in a fast-paced biotech environment.
- benefits
- 2/5
- freshness
- 4/5
- career value
- 5/5
- role clarity
- 5/5
- pay transparency
- 5/5
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 Parabilis Medicines as an employer.
What you need
- Advanced degree in Life Sciences, Pharmacy, Nursing, Medicine (PharmD, Ph.D.) required; MDs will also be considered
- 12+ years of experience in pharmacovigilance, drug safety, or safety science within the biotechnology or pharmaceutical industry
- Demonstrated expertise in safety surveillance, signal detection and management, benefit-risk assessment, and safety risk management
- Experience authoring key safety documents, including Safety Surveillance Plans (SSPs), Signal Analysis Reports (SARs), Development Risk Management Plans (dRMPs), and Development Core Safety Information (DCSI)
- Experience supporting regulatory interactions and preparing responses to global health authorities related to safety topics
- Strong working knowledge of global pharmacovigilance regulations and guidance, including FDA, EMA, and ICH requirements
Nice to have
- Prior experience in oncology, rare disease, immunology, or other specialty therapeutic areas
- Demonstrated ability to utilize AI tools for day-to-day work; baseline proficiency is expected, and advanced or innovative use of AI is a strong plus
What you get
- Base salary range of $255,000-$300,000 per year
- Annual target bonus
- Equity
- Comprehensive suite of competitive benefits designed to support overall well-being
Worth weighing
- Remote position may require strong self-management skills
- Fast-paced environment may not suit everyone
- No specific mention of work-life balance or flexibility in hours
Summarised from Parabilis Medicines's posting. Read the full original.
Listed by Parabilis Medicines on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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