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We are seeking a motivated and hands-on Manager, Preclinical Development to drive the execution of our preclinical development activities and contribute to the advancement of our innovative drug development programs. In this role, you will coordinate and oversee preclinical studies with external partners, ensuring high-quality execution in line with regulatory standards and project timelines. You will work closely with cross-functional teams and play a key role in advancing innovative therapies from research into development.
Key Responsibilities:
Key Responsibilities:
- Manage and strengthen collaborations with CROs and external experts, including coordination of proposals, CDAs , contracts and invoice.
- Plan, monitor, and evaluate preclinical in vitro and in vivo studies in compliance with ICH and GLP guidelines.
- Oversee studies across toxicology, safety, pharmacokinetics and ADME.
- Review study protocols, data, reports, and relevant regulatory and program documents (e.g. IB, Safety Data Sheets).
- Ensure timely execution and high-quality delivery of studies conducted by external partners.
- Act as the preclinical study representative within cross-functional program and study teams.
- Communicate effectively with internal and external stakeholders and represent preclinical topics in meetings.
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