For our client, a company in pharmaceuticals, we are looking for an experienced candidate to manage a Pre-clinical Safety and Toxicology Program based in the Netherlands (location flexible).
Our client is a pharmaceutical discovery and development company based in the Netherlands. They are developing a drug to address an unmet clinical need. The drug is at an early pre-clinical stage and they are seeking a flexible and experienced individual to manage their out-sourced safety & toxicology program.
- Manage a drug safety and toxicology program outsourced to multiple CROs;
- Review and agree the program strategy and study designs with CRO, Board directors and Consultant Toxicologist;
- Review and negotiate prices and terms;
- Manage the CROs : contract, delivery, budgets etc.;
- Review data with Board Directors and Consultant Toxicologist;
- Maintain a drug material forecast and liaise with the CMC group to ensure material supply.
- MSc or PhD in Life Science;
- At least 3 till 5 years' of work experience either in a pre-clinical CRO or working for a pharma or biotech company managing pre-clinical projects internally or externally;
- Experience managing safety and toxicology studies either in house or out-sourced.
What do we offer
- One year contract with intention for a permanent employment (32-40 hours per week);
- Attractive salary package;
- Start date: asap;
- An international environment where you can learn a lot in challenging projects.
When interested please react through the application process with your English resume.
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