or apply directly on Beam Therapeutics's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 82 days Beam Therapeutics's roles stay open a median of 82 days
- Reposted
- No
- Salary listed
- No 0% of Beam Therapeutics's roles list one
- Ghost-job risk at Beam Therapeutics
- high 26 stale, 0 reposted of 27 open
- Hiring momentum
- 35 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-10-24
Measured from postings appearing on and disappearing from Beam Therapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Beam Therapeutics.
About this role
The Director of Pharmacovigilance at Beam Therapeutics will oversee safety monitoring and operations for clinical trials, providing strategic support for pharmacovigilance activities. This role involves collaboration with various departments, managing safety reports, and ensuring compliance with global regulations. The position also includes developing training materials, contributing to quality assurance, and participating in risk assessment initiatives.
- benefits
- 1/5
- freshness
- 1/5
- 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 Beam Therapeutics as an employer.
What you need
- Degree in Pharmacy, Nursing, Epidemiology, Biosciences or equivalent degree with pharmaceutical industry background and proven competence in PV
- Typically 12+ years’ pharmaceutical industry experience, including a minimum of 5 years’ experience in PV
- Knowledge of MedDRA dictionary, clinical trial methodology, medical terminology, and general principles of clinical assessment of AEs
- Demonstrated knowledge of global PV regulatory environment with working knowledge of international regulations including but not limited to FDA, EU, GVP, ICH guidelines
- Working knowledge of industry standard safety databases (ARGUS and ARISg) and other electronic data capture systems
- Experience reviewing cumulative safety data with ability to interpret, synthesize and communicate complex clinical /pharmaceutical information and safety data
Worth weighing
- Onsite requirements: Candidates are expected to come onsite 1-3 days per week
- No specific benefits listed
- Salary range provided but based on multiple factors, which may not be transparent to candidates
Summarised from Beam Therapeutics's posting. Read the full original.
Listed by Beam Therapeutics on their greenhouse job board, last confirmed open on 2026-10-24. PitchMeAI is not the employer.
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