Toxicology Operations Lead (Remote/Onsite)

Regeneron Pharmaceuticals, Inc.; United States; Hybrid; USD 98,000 - 160,000; Full time

Benefits offered by this job

Annual bonuses

Equity awards

Pension benefits

401(k) company match

Health & wellness programs

Fitness centers

Insurance benefits

Paid time off

Family support

Job summary

Regeneron Pharmaceuticals, Inc. in the United States is seeking an Associate Manager, Toxicology Operations to support the Toxicology department. You will monitor outsourced GLP and non-GLP studies, develop study concepts, and coordinate all logistical aspects of studies.

The role requires a biology degree with 6-8+ years in pharma/drug development, strong toxicology knowledge, and the ability to lead junior staff, with remote work option and EST hours preferred.

Qualifications

• Bachelor's degree in biological sciences with 6-8+ years post-degree experience in pharmaceutical/drug development.
• Strong understanding of toxicology investigations and regulated nonclinical safety studies.
• Experience designing, monitoring and interpreting toxicology studies and study concepts.

Responsibilities

• Lead operational role for the Toxicology department, directing junior specialists with minimal supervision.
• Collect and maintain metrics for toxicology studies (timelines, costs, etc.).
• Maintain department SOPs database.
• Lead study monitor on GLP toxicology studies and contribute to study design concepts.
• Coordinate all logistical aspects of outsourced studies.
• Develop protocols for outsourced toxicology studies with limited supervision.
• Monitor studies remotely or on-site at CRO to ensure protocol compliance.
• Review toxicology study data/reports and identify areas for further evaluation.
• Participate in department meetings to discuss operational strategies.

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 support the Toxicology department. You will monitor outsourced GLP and non-GLP studies, develop study concepts, and coordinate all logistical aspects of studies.

The role requires a biology degree with 6-8+ years in pharma/drug development, strong toxicology knowledge, and the ability to lead junior staff, with remote work option and EST hours preferred.