Nonclinical Toxicology Study Monitor — Hybrid Oversight
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Research/Development
Clinical Research, Research Scientist, Pharmaceutical Science/ Research, Regulatory Compliance Specialist -
Pharmaceutical
Pharmaceutical Science/ Research, Regulatory Compliance Specialist
Job Description & How to Apply Below
Vertex Pharmaceuticals is seeking a Nonclinical Toxicology Study Monitoring Scientist to oversee outsourced nonclinical safety studies across small and large molecule programs, including cell and gene therapies. You will partner with project toxicologists and CROs to ensure scientific rigor, GLP compliance, and timely study execution in a fast-paced, matrixed environment.
The role emphasizes study monitoring, data integrity, issue resolution, and cross-functional communication to support
This is an excellent opportunity to take on the Nonclinical Toxicology Study Monitor — Hybrid Oversight role at Vertex Pharmaceuticals.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Nonclinical Toxicology Study Monitor — Hybrid Oversight role in the description above.
We appreciate your interest in this position.
Join Vertex Pharmaceuticals and contribute to our ongoing work.
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