Toxicology Operations Lead - Remote

Regeneron Pharmaceuticals, Inc.; United States; Hybrid; USD 120,000 - 180,000; Full time

Benefits offered by this job

Annual bonuses or incentive plans

Equity awards

Pension/retirement benefits

401(k) company match

Health and wellness programs

Fitness centers

Insurance benefits (medical, dental, 视

Paid time off

Family support benefits

Job summary

Regeneron Pharmaceuticals, Inc. in the United States is seeking an Associate Manager, Toxicology Operations to lead departmental operations and oversee study monitoring for outsourced toxicology studies.

The role supports GLP and non-GLP programs with limited supervision, coordinating logistics and maintaining SOPs. The candidate should have a strong background in toxicology study design, monitoring, and interpretation, and excellent communication skills to interact with cross-functional teams.

Qualifications

• Bachelor's degree in biological sciences; 6–8+ years post-degree experience; Master's preferred.
• Strong understanding of toxicologic investigation theory and rationale.
• Significant experience in design, monitoring, and interpretation of regulated nonclinical safety studies.
• Ability to communicate effectively with stakeholders at all levels of drug safety and pharmacometrics.

Responsibilities

• Lead operational role for the Toxicology department with limited supervision.
• Oversee completion of department goals and direct junior specialists.
• Collect and maintain metrics for toxicology studies (timelines, costs, etc.).
• Maintain department SOPs database and contribute to study design concepts.
• Coordinate all aspects of logistical support for outsourced studies (GLP and non-GLP).

Skills

Leadership

Operations management

Study monitoring

Communication

Education

Bachelor's degree in biological sciences

Master's degree preferred

Job description

Regeneron Pharmaceuticals, Inc. in the United States is seeking an Associate Manager, Toxicology Operations to lead departmental operations and oversee study monitoring for outsourced toxicology studies.

The role supports GLP and non-GLP programs with limited supervision, coordinating logistics and maintaining SOPs. The candidate should have a strong background in toxicology study design, monitoring, and interpretation, and excellent communication skills to interact with cross-functional teams.