Toxicology Study Manager — Preclinical & CRO Lead (Onsite)

Scorpion Therapeutics; California (MO); On-site; USD 120,000 - 180,000; Full time

Job summary

Scorpion Therapeutics is seeking a Preclinical Study Manager to oversee non-GLP and GLP toxicology studies from research to late-phase development, ensuring regulatory compliance and scientific objectives at onsite Redwood City, CA.

You will coordinate with CROs and internal teams, facilitate data analysis, support regulatory submissions, and manage vendor relations, contracts, and SOP development while leading study oversight in oncology and international compliance. Travel as needed.

Qualifications

• BS in science is required.
• 5+ years in biotech/pharma/CRO industries.
• Strong knowledge of GLP, ICH, FDA guidelines.

Responsibilities

• Coordinate with CROs and internal teams to design, monitor, and review toxicology studies.
• Facilitate data analysis and regulatory submissions.
• Manage vendor relations, contracts, and SOP development.
• Support study reports and audits.

Skills

Cross-functional communication

Negotiation

Project management

Education

BS in science

Job description

Scorpion Therapeutics is seeking a Preclinical Study Manager to oversee non-GLP and GLP toxicology studies from research to late-phase development, ensuring regulatory compliance and scientific objectives at onsite Redwood City, CA.

You will coordinate with CROs and internal teams, facilitate data analysis, support regulatory submissions, and manage vendor relations, contracts, and SOP development while leading study oversight in oncology and international compliance. Travel as needed.