Executive Director, Global Safety Physician

i-Pharm Consulting

Philadelphia (Philadelphia County)

Hybrid

USD 250,000 - 360,000

Full time

6 days ago
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Job summary

i-Pharm Consulting is seeking a Senior/Executive Director of Global Clinical Safety to lead safety strategy across clinical development and post-marketing programs. This role will oversee signal detection, risk management, and global safety governance with regulatory interactions.

The successful candidate will bring MD (or equivalent) credentials and 12–18+ years in safety/pharmacovigilance, with strong matrixed leadership experience and industry regulatory knowledge.

Qualifications

  • MD (or equivalent) required.
  • 12–18+ years of clinical safety/pharmacovigilance experience.
  • Deep expertise in signal detection, safety surveillance, and benefit–risk assessment.
  • Strong understanding of global safety regulations and reporting requirements.
  • Proven ability to operate in a matrixed, cross-functional environment.
  • Experience contributing to regulatory filings and health authority interactions.

Responsibilities

  • Serve as the medical and scientific expert for safety across assigned programs.
  • Lead signal detection, evaluation, and risk management activities.
  • Drive benefit–risk assessments and contribute to safety governance forums.
  • Author and/or review regulatory safety documents (DSURs, PBRERs, IBs).
  • Partner with Clinical Development, Regulatory Affairs, Biostatistics, and PV Operations.
  • Support global regulatory interactions and responses to health authority queries.
  • Ensure inspection readiness and compliance with global pharmacovigilance regulations.
  • Contribute to the development and scaling of safety processes and best practices.

Skills

Clinical safety/pharmacovigilance
Signal detection
Safety surveillance
Global safety regulations
Leadership
Regulatory filings

Education

MD (or equivalent)

Job description

Location: Greater Philadelphia area (Hybrid; 3 days/week on-site)

Overview

A growing, clommercial-stage biopharmaceutical company is seeking a Senior/Executive Director of Global Clinical Safety to play a key leadership role across both clinical development and post-marketing programs. This individual will provide strategic and medical oversight of safety across the portfolio, driving signal detection, benefit–risk assessment, and global safety strategy.

This is a highly visible role within a fast-paced, collaborative environment, with the opportunity to influence regulatory strategy and safety governance at a global level.

Key Responsibilities
  • Serve as the medical and scientific expert for safety across assigned programs (early through late-stage and/or marketed products)
  • Lead signal detection, evaluation, and risk management activities, including interpretation of safety data from multiple sources
  • Drive benefit–risk assessments and contribute to safety governance forums (e.g., safety review committees)
  • Author and/or review key regulatory safety documents (e.g., DSURs, PBRERs, IBs, safety sections of submissions)
  • Partner cross-functionally with Clinical Development, Regulatory Affairs, Biostatistics, and PV Operations to align on safety strategy
  • Support global regulatory interactions, including responses to health authority queries
  • Ensure inspection readiness and compliance with global pharmacovigilance regulations (FDA, EMA, ICH, etc.)
  • Contribute to the development and scaling of safety processes, infrastructure, and best practices
Qualifications
  • MD (or equivalent)
  • ~12–18+ years of experience in clinical safety/pharmacovigilance within biotech or pharma
  • Deep experience across signal detection, safety surveillance, and benefit–risk assessment
  • Strong understanding of global safety regulations and reporting requirements
  • Proven ability to operate in a matrixed, cross-functional environment
  • Prior experience contributing to or leading regulatory filings and health authority interactions
  • Demonstrated leadership skills, with experience influencing stakeholders and/or managing teams
Why This Role
  • High-impact, strategic leadership position with visibility across the organization
  • Opportunity to shape global safety strategy for innovative therapies
  • Collaborative, growth-oriented biotech environment with strong pipeline momentum
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