Senior Scientist, Safety Assessment & Toxicology Data Analytics

Scorpion Therapeutics; United States; Remote; USD 120,000 - 180,000; Full time

Job summary

Centessa Pharmaceuticals is seeking a Senior Scientist within Safety Assessment to focus on non-laboratory toxicology data analysis and strategy. The role leads data visualization and analytics for multi-dose toxicology studies and supports regulatory planning.

You will audit SEND datasets from CROs for regulatory compliance, conduct literature reviews to assess safety risks, and collaborate with Toxicology, DMPK, CMC, and Project Development teams to influence early pipeline decisions and

Qualifications

• Minimum degree in toxicology, pharmacology or related sciences.
• 6–8+ years (MS) or 8–10+ years (BS) in biotech/pharma toxicology or data management.
• Expert understanding of preclinical toxicology datasets, SEND data validation, and data visualization tools.

Responsibilities

• Lead data visualization and analytics of multi-dose toxicology studies.
• Audit SEND datasets from CROs for regulatory compliance.
• Conduct mechanistic literature reviews to assess safety risks.
• Support cross-functional collaboration with Toxicology, DMPK, CMC, and Project Development teams.
• Influence early pipeline decisions and contribute to regulatory submissions.

Skills

Toxicology data analysis

SEND data validation

Data visualization

Education

Bachelor's or Master's in Toxicology/Pharmacology or related sciences

Tools

Python

R

GraphPad

Job description

Senior Scientist within Safety Assessment at Centessa Pharmaceuticals

focusing on non-laboratory toxicology data analysis and strategy.

Responsibilities

• lead data visualization and analytics of multi-dose toxicology studies
• audit SEND datasets from CROs for regulatory compliance
• conduct mechanistic literature reviews to assess safety risks
• support cross-functional collaboration with Toxicology, DMPK, CMC, and Project Development teams
• influence early pipeline decisions and contribute to regulatory submissions

Requirements

• B.S. or M.S. in Toxicology, Pharmacology, or related sciences
• 6–8+ years (M.S.) or 8–10+ years (B.S.) experience in biotech/pharma toxicology or data management
• expert understanding of preclinical toxicology datasets, SEND data validation, and data visualization tools (e.g., Python, R, GraphPad)

Preferred

• strong scientific writing and cross-disciplinary communication skills
• experience with regulatory safety datasets

High-Value

• focus on neurotherapeutics (narcolepsy, sleep disorders)
• nonclinical safety
• regulatory compliance, and cross-functional data integration

Work Setup

remote US-based role with occasional travel.