Senior Study Director, Toxicology & Regulatory Science

Scorpion Therapeutics; Pennsylvania; On-site; USD 150,000 - 190,000; Full time

Job summary

Scorpion Therapeutics is seeking a Study Director in toxicology based in Pennsylvania. You will oversee acute to chronic general toxicology studies across modalities, ensuring GLP compliance and timely execution while coordinating with science, veterinary, and regulatory teams.

The role requires 8+ years of experience, 5+ years as a Study Director, and strong leadership and communication skills for regulatory submissions and cross-functional collaboration.

Qualifications

• Master’s degree in toxicology, pharmacology, or related discipline.
• 8+ years of relevant experience in toxicology or drug safety.
• 5+ years as a Study Director in pharma/biotech/CRO.
• GLP General Toxicology Study Director experience with varied models/designs.
• Strong knowledge of GLP and US FDA 21 CFR Part 58.
• Strong collaboration, communication, and leadership skills.
• Excellent verbal and written presentation abilities.

Responsibilities

• Serve as Study Director for acute to chronic general toxicology studies across modalities.
• Interact with scientific staff to ensure protocol and SOP compliance.
• Analyze and interpret data; prepare regulatory submission reports.
• Ensure regulatory rigor and timely study execution.
• Collaborate across functions to identify opportunities and provide solutions.
• Lead method development and cross-group initiatives as needed.

Skills

Study Director

GLP Compliance

Regulatory Submissions

Toxicology

Cross-functional

Data interpretation

Leadership

Communication

Protocol development

Teamwork

Education

Master’s degree in toxicology

Job description

Scorpion Therapeutics is seeking a Study Director in toxicology based in Pennsylvania. You will oversee acute to chronic general toxicology studies across modalities, ensuring GLP compliance and timely execution while coordinating with science, veterinary, and regulatory teams.

The role requires 8+ years of experience, 5+ years as a Study Director, and strong leadership and communication skills for regulatory submissions and cross-functional collaboration.