Director, Drug Safety & Pharmacovigilance Scientist
Dyne Therapeutics · Waltham, MA
Posted 27 days ago
or apply directly on Dyne Therapeutics's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 27 days Dyne Therapeutics's roles stay open a median of 45 days
- Reposted
- No
- Salary listed
- No 0% of Dyne Therapeutics's roles list one
- Ghost-job risk at Dyne Therapeutics
- high 58 stale, 1 reposted of 69 open
- Hiring momentum
- 88 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 Dyne Therapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Dyne Therapeutics.
About this role
The Director, Drug Safety & Pharmacovigilance Scientist at Dyne Therapeutics is responsible for leading safety surveillance and risk management activities for clinical development programs. This role involves analyzing safety data, contributing to regulatory submissions, and collaborating with various departments to ensure compliance and enhance pharmacovigilance processes. The position emphasizes strategic leadership in safety oversight and the communication of safety profiles for investigational therapies.
- benefits
- 1/5
- freshness
- 4/5
- 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 Dyne Therapeutics as an employer.
What you need
- Advanced degree in life sciences, health sciences, pharmacy, medicine, nursing, or a related discipline
- 10+ years of relevant pharmacovigilance, drug safety, clinical development, or related biotechnology or pharmaceutical industry experience
- Demonstrated expertise in safety surveillance, signal detection, signal evaluation, aggregate safety review, benefit-risk assessment, and risk management for clinical-stage development programs
- Experience authoring or contributing to DSURs, PSURs/PBRERs, safety signal assessments, regulatory safety responses, and safety-related sections of clinical or regulatory documents
- Deep knowledge of global pharmacovigilance regulations and guidance, including FDA, EMA, ICH, GVP, GCP, and applicable safety reporting requirements
- Experience reviewing, analyzing, and interpreting clinical and safety data, including ICSRs, aggregate datasets, safety listings, tables, figures, and data visualizations
Nice to have
- Experience in rare disease, neuromuscular disease, or clinical-stage biotechnology
Worth weighing
- No specific benefits listed in the posting
- Salary range provided, but individual compensation may vary based on factors such as education and experience
- Role involves significant cross-functional collaboration, which may require strong interpersonal skills
Summarised from Dyne Therapeutics's posting. Read the full original.
Listed by Dyne Therapeutics on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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