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Accountabilities:
- Lead end-to-end operational execution of nonclinical toxicology studies, ensuring alignment with scientific, regulatory, and program objectives.
- Oversee study outsourcing activities including RFP processes, CRO selection, contracting, protocol development, monitoring, and final reporting.
- Serve as lead study monitor and sponsor representative for GLP and non-GLP toxicology studies conducted at external partners.
Requirements:
- Bachelor’s or Master’s degree in biological sciences or a related field, with 7+ years of experience in pharmaceutical or drug development environments.
- Strong background in toxicology study design, monitoring, interpretation, and regulatory nonclinical safety frameworks.
- Experience managing CRO-based studies, including outsourcing, contracting, and external scientific oversight.
Benefits:
- Competitive annual salary aligned with experience and expertise ($114,800 – $187,400 USD range referenced).
- Comprehensive health coverage including medical, dental, vision, life, and disability insurance.
- Paid time off and family leave programs.
Other
Our partner operates at the intersection of science, operations, and drug development, supporting the execution of critical toxicology studies that inform preclinical safety and regulatory decisions. The environment is highly collaborative, science-driven, and fast-paced, with strong exposure to global project teams and regulatory processes.