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Senior/Executive Medical Director, Pharmacovigilance

CRISPR Therapeutics
Full-time
Remote friendly (Boston, MA)
United States
$230,000 - $300,000 USD yearly
Medical Affairs

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Role Summary

Senior/Executive Medical Director, Pharmacovigilance. Oversees all safety and pharmacovigilance activities in clinical development and post-marketing surveillance, ensuring medical safety assessments, regulatory reporting, risk management, and communication of safety information globally. Manages safety activities including external suppliers and translates a safety mindset across the organization.

Responsibilities

  • Establish and maintain safety governance oversight for all CRISPR Therapeutics products
  • Provide hands-on leadership and expertise in all PV matters and drive a safety mindset across teams
  • Collaborate with clinical, medical, quality, regulatory, and other stakeholders to oversee safety and PV issues, including study protocols, development plans, INDs/CTAs/BLAs, and other PV activities
  • Plan and forecast global PV resources and budget; coordinate with groups on resource needs
  • Interact with internal and external colleagues to develop PV programs and processes to meet regulatory reporting requirements
  • Manage PV Operations and provide strategic direction for PV efforts
  • Lead process improvements within global pharmacovigilance, including technology assessment and implementation
  • Oversee PV consultants on aggregate reporting, risk-benefit management, signal detection, and risk mitigation for clinical and post-marketing products
  • Ensure regulatory compliance of PV operations
  • Lead and support health authority and development partner audits
  • Implement global process standardization and continuous improvement

Qualifications

  • MD degree or equivalent
  • 3+ years of clinical practice experience
  • At least 6 years of direct pharmaceutical industry experience
  • Preferred: experience in both biotech and pharmaceutical companies

Skills

  • Cross-functional collaboration and relationship building
  • Safety governance and risk management expertise
  • Regulatory knowledge across PV, clinical development, and quality
  • Strategic planning and resource management
  • Process improvement and change management

Education

  • MD degree or equivalent

Additional Requirements

  • Location considerations and on-site expectations as applicable
  • Travel requirements not specified in the source
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