Remote Associate Director, Pharmacovigilance & Safety Leadership

Ladders

United States

Remote

USD 179,000 - 233,000

Full time

16 hours ago
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Benefits offered by this job

Medical, dental, vision
PTO & family-forming benefits
401(k) with equity
Learning institute
Employee resource groups

Job summary

Ladders is seeking an Associate Director, Pharmacovigilance/Product Safety to lead safety surveillance across clinical and non-clinical programs in a regulated biopharma environment. This remote US-based role requires medical judgment, regulatory expertise, and cross-functional leadership to ensure timely assessment and reporting of emerging safety information.

The successful candidate will partner with internal stakeholders and external vendors, drive benefit–risk analyses, and contribute to

Qualifications

  • 3–5 years of experience in pharmacovigilance or safety roles.
  • Device experience preferred.

Responsibilities

  • Provide medical significance and expectedness assessments of AE/SAE reports.
  • Compile analyses of similar events and ad hoc safety analyses.
  • Contribute medical input to risk management plans and safety monitoring activities.
  • Deliver periodic benefit-risk assessment reports.
  • Investigate and review emerging safety data from clinical and non-clinical sources.
  • Author and review drug safety-related regulatory reports and documents.
  • Coordinate with an external drug safety vendor on review and safety assessment activities.

Skills

Leadership
Communication
Regulatory knowledge
MedDRA knowledge
Vendor coordination

Education

Master’s degree in life sciences, RN, PharmD, or MD

Job description

Ladders is seeking an Associate Director, Pharmacovigilance/Product Safety to lead safety surveillance across clinical and non-clinical programs in a regulated biopharma environment. This remote US-based role requires medical judgment, regulatory expertise, and cross-functional leadership to ensure timely assessment and reporting of emerging safety information.

The successful candidate will partner with internal stakeholders and external vendors, drive benefit–risk analyses, and contribute to

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