Overview In this role you drive safety assessment studies in nonclinical toxicology, serving as the study's lead and sole point of control. You will own the technical conduct, data interpretation, documentation, and reporting in line with GLPs and regulatory guidelines, while maintaining sponsor alignment. You act as the primary client contact, shaping study requirements and ensuring quality and compliance. This position combines scientific leadership with a strong emphasis on collaboration, client service, and operational excellence to support Labcorp's mission to advance healthcare.
Compensation / Benefits- Medical
- Dental
- Vision
- Life
- STD/LTD
- 401(k)
Responsibilities- Serve as Study Director, PI, or Contributing Scientist for nonclinical toxicology studies under GLPs
- Be the single point of control for safety assessment studies and legally responsible for the study
- Oversee technical conduct, interpretation, analysis, documentation, reporting, and archival per policies and regulatory guidelines
- Act as main client contact and advisor, understanding Sponsor requirements
- Ensure compliance with GLPs, Home Office License requirements (if applicable), and regulatory agency guidelines
Key requirements- Master's degree in toxicology, biology, chemistry, biochemistry, or molecular biology with 3+ years of scientific research experience
- Preferred: PhD in toxicology, regenerative biology, genetics, virology, or immunology
- 1+ years of experience as Study Director or Principal Investigator (preferred)
- Experience at a Contract Research Organization (CRO)
- Experience overseeing or contributing to pharmaceutical non-clinical drug development
- Strong client relationship management skills
- Excellent organizational and time management skills
- Strong verbal and written communication skills
- Ability to promote high professional standards and foster staff relationships
- Ability to understand financial status of ongoing studies
- client relationship management
- communication
- organizational skills
- GLP compliance
- nonclinical toxicology study conduct
- data interpretation and reporting
