Global PV Operations Leader: Strategy & Compliance

Scorpion Therapeutics; Boston (MA); On-site; USD 238,000 - 374,000; Full time

Benefits offered by this job

Medical/dental/vision

401(k) match

Disability

Life insurance

Tuition reimbursement

Paid volunteer time off

Paid holidays

Well-being benefits

Sick time

Vacation

Job summary

Scorpion Therapeutics seeks a strategic leader to oversee global pharmacovigilance operations across the product lifecycle. You will manage case processing, regulatory reporting, vendor oversight, and continuous improvement to ensure safety data quality and compliance.

The role requires extensive PV experience, leadership ability, and cross-functional collaboration with Regulatory Affairs, QA, Medical Affairs, and Clinical Development. Boston-based, with travel as needed.

Qualifications

• Bachelor’s degree in life sciences/healthcare/pharmacy (advanced degree preferred).
• 15+ years in pharma/healthcare; 10+ years progressive PV operations/safety reporting.
• Experience with global case processing/regulatory reporting and leading global teams.

Responsibilities

• Provide strategic leadership for global pharmacovigilance operations across the product lifecycle.
• Lead global PV operations including ICSR management, regulatory reporting, and QA review.
• Oversee vendor governance, outsourcing, budgets, and CRO performance.
• Ensure compliance with FDA/EMA/ICH PV regulations and inspection readiness.
• Drive continuous improvement, digital transformation, and metric dashboards.
• Develop and mentor a global PV team and cross-functional partnerships.

Skills

Leadership

Communication

Stakeholder management

Analytical thinking

Problem solving

Financial management

Project management

Education

Bachelor’s degree in life sciences/healthcare/pharmacy

Tools

Argus

ArisG

Job description

Scorpion Therapeutics seeks a strategic leader to oversee global pharmacovigilance operations across the product lifecycle. You will manage case processing, regulatory reporting, vendor oversight, and continuous improvement to ensure safety data quality and compliance.

The role requires extensive PV experience, leadership ability, and cross-functional collaboration with Regulatory Affairs, QA, Medical Affairs, and Clinical Development. Boston-based, with travel as needed.