How would you like to have a career that really makes a difference? Attentive Science is a nimble Non-Clinical Contract Research Organization (CRO) providing support to the Pharmaceutical, Animal Health, Agrochemical and Food Industries to help them create a healthier future for us all. Our experienced scientists provide the highest quality results coupled with segment leading expediency and flexible solutions to meet the specific needs of our clients.
The Study Director - Toxicology is responsible for the overall conduct, scientific integrity, and regulatory compliance of nonclinical research studies-both regulated and nonregulated. This role involves the design, planning, execution, interpretation, and reporting of a wide range of toxicology studies supporting drug development, chemical safety, and product safety assessments.

THE REQUIREMENTS OF THE POSITION

• Bachelor’s degree in toxicology, pharmacology, biology, or a related field required with 5+ years of experience in a non-clinical research environment.
• Advanced degree (M.S., Ph.D., D.V.M.) and experience preferred..
• Strong understanding of toxicology principles and regulatory guidelines (FDA, OECD, EPA, etc.).
• Exceptional organizational, analytical, and communication skills.
• Proficiency with electronic data systems and laboratory information management systems (LIMS) preferred
• Preferred Certifications:
• Certification by the American Board of Toxicology (DABT) or eligibility is a plus.
  Join the Attentive Science team and grow your career with us while contributing to the discovery and development of life saving remedies. Attentive Science provides a comprehensive benefits package including Healthcare, Dental, Vision, 401k, Tuition Reimbursement and on-the-job career development

• Serve as the single point of control and accountability for assigned toxicology studies.
• Design and develop scientifically sound study protocols in collaboration with sponsors, proposal management, and internal scientific teams.
• Ensure studies are conducted in full compliance with regulatory requirements, internal SOPs, and GLP standards.
• Monitor the progress of studies, identify and resolve issues, and ensure adherence to timelines and deliverables.
• Interpret data and prepare high-quality study reports suitable for regulatory submissions.
• Collaborate closely with cross-functional teams, including laboratory scientists, pathologists, veterinarians, quality assurance personnel, and external sponsors.
• Participate in client meetings, audits, and regulatory inspections as needed.
• Maintain all study-related documentation and ensure appropriate archiving of records and materials.
• Drive process improvements and contribute to departmental and organizational initiatives
• Perform other duties as needed