I am partnered with a rapidly growing clinical stage biopharma seeking to expand their research team with an experienced toxicologist to take ownership and responsibility for the efficient and timely delivery of toxicology contributions across a number of drug development programs.
*Your responsibilities*:
* Oversee and manage toxicology study activities, including contracts and logistics with CRO partners
* Manage projects to allow internal teams the ability to monitor study progress and timely delivery of milestone supporting regulatory submissions
* Maintain lines of communication between toxicology team to ensure quick adjustments to plans and deliverables etc in line with latest regulations and strategies
* Work closely with senior management to discuss and analyse risks, issues and possible mitigation
* Remain point of contact for external partners, including CROs
* Provide oversight on final reports/SEND/eCTD from vendors
*Your Background:*
* PhD ideal, BSc or MSc considered
* Industry experience within toxicology (pharma/biotech/CRO)
* Understanding of regulatory requirements
* Beneficial: previous project management experience