Associate Director, Translational Toxicology

ACADIA Pharmaceuticals Inc.; Princeton (NJ); Hybrid; USD 155,000 - 193,200; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401(k) Plan with company match

Employee Stock Purchase Plan

Job summary

ACADIA Pharmaceuticals Inc. is seeking an Associate Director based in New Jersey, CA or San Diego to oversee Translational Science preclinical safety deliverables. This role requires collaboration in research and development, driving alignment across projects and ensuring timely communication to meet regulatory deliverables.

The ideal candidate will have at least 8 years of experience in toxicology within the pharma industry. Benefits include competitive pay and a hybrid work environment.

Qualifications

• 8 years of relevant experience in preclinical safety assessment/toxicology.
• DABT Certification strongly preferred.
• Experience in the composition and review of toxicology reports.

Responsibilities

• Manage experimental safety assessment/toxicology programs.
• Provide oversight on scientific management of studies.
• Monitor CROs for quality in studies conducted.

Skills

Understanding of the drug development process

Knowledge of GLP, ICH and FDA guidelines

Excellent communication skills

Cross-functional project team experience

Education

BS or MS in a relevant discipline

Tools

Statistical tools for data analysis

Job description

ACADIA Pharmaceuticals Inc. is seeking an Associate Director based in New Jersey, CA or San Diego to oversee Translational Science preclinical safety deliverables. This role requires collaboration in research and development, driving alignment across projects and ensuring timely communication to meet regulatory deliverables.

The ideal candidate will have at least 8 years of experience in toxicology within the pharma industry. Benefits include competitive pay and a hybrid work environment.