RedBrick Staffing · 18 hours ago
Toxicologist
RedBrick Staffing is seeking a Toxicologist to design and manage studies while supporting regulatory submissions. The role involves acting as the primary contact for clients, ensuring GLP compliance, and communicating study findings to various stakeholders.
Responsibilities
Design & manage studies
Support regulatory submissions
Prepare nonclinical packages
Act as the primary contact for clients – helping build & establish long-term relationships
Partner with clients to understand goals
Conserve successful completed studies, from initial development to client delivery
Facilitate coordination across in-vivo & in-vitro ops
Monitor studies to identify risks, troubleshoot issues, & manage timelines
Combine data to create significant, justifiable conclusions
Create, review, and sign-off on study reports
Communicate study findings to clients, regulatory bodies, & via team presentations
Ensure all studies are GLP compliant
Act of company representative for audits & inspections
Qualification
Required
4+ years of experience designing & leading GLP toxicology studies
Experience acting as Study Director for GLP studies (with successful FDA submissions)
Experience supporting IND/NDA/BLA nonclinical packages
Proven ability to lead complex study programs
Excellent verbal & written communication skills
Preferred
Ph.D. in Toxicology, Pharmacology, or similar preferred
D.A.B.T. Cert. strongly preferred
Company
RedBrick Staffing
With over two decades of internal recruitment support, RedBrick Staffing has been able to fine-tune a tried-and-true strategy of locating talent through a personalized recruitment process.