Principal Scientist - Safety Surveillance and Risk Assessment

We are hiring a Principal Scientist with demonstrated experience in Adverse Experience Management to join our Pre-Clinical group in Richmond, VA, or we are open to remote work arrangements.

About the role

The selected candidate will use their scientific and technical expertise to lead our adverse experience management program as well as conduct and write toxicological risk assessments in support of regulatory submissions and product stewardship activities.

Responsibilities

• Lead our Product Safety Surveillance Committee and independently manage our Adverse Experience program to meet regulatory requirements, complete pre-market tobacco applications and continuously evolve our understanding of the health effects of Altria’s portfolio of products
• Independently develop toxicological risk assessments in support of Altria’s highly regulated business
• Apply in depth knowledge of risk assessment methodologies to evaluate materials, ingredients and products
• Integrate different lines of toxicological evidence including read-across and QSAR to formulate science-based decisions to guide product development and as a part of regulatory submissions
• Lead and participate on teams within Pre-Clinical to develop best practices, operating procedures and protocols for our adverse experience management program as well as new or modified risk assessment methods
• Monitor and adjust to changes in the regulatory landscape
• Provide product stewardship support across products, materials, ingredients, technologies, manufacturing processes, signal detection in adverse experiences, etc. for Altria’s Operating Companies
• Lead and participate on cross-functional teams, providing toxicological expertise while representing the Pre-Clinical team and Regulatory Sciences
• Monitor the scientific literature as well as maintain and expand relationships with key opinion leaders in academia in the areas of risk assessment and tobacco regulatory research
• Participate in national and international scientific meetings and conferences to maintain and expand technical expertise

Requirements

• PhD in toxicology or related field with 10+ years of experience in toxicology with demonstrated expertise in pharmacovigilance/adverse experience program management
• In depth knowledge of risk assessment and toxicological principles with strong experience applying them in a regulatory environment
• Strong experience in industrial and/or regulatory toxicology, U.S. and international regulatory environments
• Experience with applying predictive toxicology methods (e.g., read-across and/or QSAR approaches) to address toxicological issues (preferred)
• Demonstrated ability to analyze/synthesize data from multiple lines of human and/or non-human evidence to develop meaningful insights and conclusions
• Expertise in interpreting relevant studies to assess product safety
• Proven experience in preparing written regulatory submissions
• Outstanding verbal and written communication skills for presenting and communicating results/data to both scientists and non-scientists
• Strong leadership skills and the ability to use those skills in cross-functional teams

Pay

The Salary Range for this position is: $132,500.00 - $202,100.00.

Benefits

• Flexible and remote work options
• 15 days of paid time off, 13 paid holidays, 2 floating holiday days, and a 37.5-hour workweek
• Annual merit increases and performance bonus
• 401(k) matching from day one, plus Deferred Profit Sharing (13%-17% of base salary)
• Student loan repayment assistance and professional development stipends
• Comprehensive medical, dental, and vision coverage for you and your family
• Paid parental and bonding leave
• Wellness programs for whole well-being
• Paid volunteer days