Remote Principal Scientist: Safety Surveillance & Risk

Altria; United States; On-site; USD 133,000 - 202,000; Full time

Job summary

Altria is seeking a Principal Scientist - Safety Surveillance and Risk Assessment to lead our adverse experience management program within Pre-Clinical in Richmond, VA, with remote options. You'll develop toxicological risk assessments for regulatory submissions, integrate read-across and QSAR, and guide product stewardship while collaborating with cross-functional teams.

This role requires a PhD in toxicology with 10+ years of experience and strong writing and communication for scientific and

Qualifications

• PhD in toxicology or related field with 10+ years of toxicology experience and pharmacovigilance/adverse experience program management.
• Strong knowledge of risk assessment and toxicology in regulatory environments.
• Experience with regulatory toxicology and written regulatory submissions.

Responsibilities

• Lead the Adverse Experience program to meet regulatory requirements and support pre-market applications.
• Develop toxicological risk assessments to support regulatory submissions and product stewardship.
• Apply risk assessment methodologies to evaluate materials, ingredients and products.
• Integrate read-across and QSAR to inform science-based decisions for product development.
• Lead teams to develop best practices, SOPs, and protocols for adverse experience management.
• Monitor regulatory changes and maintain relationships with key opinion leaders.
• Collaborate on cross-functional teams to provide toxicological expertise for regulatory science.
• Present findings at national/international meetings to maintain technical expertise.

Skills

Adverse experience management

Toxicology risk assessment

Regulatory submissions

Pharmacovigilance

Leadership

Cross-functional collaboration

Scientific writing

Data synthesis

Education

PhD in toxicology or related field

Job description

Altria is seeking a Principal Scientist - Safety Surveillance and Risk Assessment to lead our adverse experience management program within Pre-Clinical in Richmond, VA, with remote options. You'll develop toxicological risk assessments for regulatory submissions, integrate read-across and QSAR, and guide product stewardship while collaborating with cross-functional teams.

This role requires a PhD in toxicology with 10+ years of experience and strong writing and communication for scientific and