Pharma / Medical

For our customer based in Ticino we are currently looking for a:

Preclinical Development Manager

who will join the R&D department and reporting directly to the Head of Development.

Duties and Responsibilities:

  • Execute and monitor nonclinical safety studies and interpret findings from these studies in support of clinical development.
  • Provide day-to-day management of preclinical/early clinical development of new drug compounds:
  • Apply project management best practices in the planning, initiation, execution, and tracking of project activities, timelines and related budget;
  • Support regulatory submissions, ensuring all crucial timelines are met;
  • Assist regulatory affairs in meeting submission deadlines Closely monitor and interact with Contract Research Organizations, granting agencies and consultants;


  • Master's degree in toxicology, biology or a related life-science field (Pharmacology/ Pharmaceutics/ Biochemistry, DVM, PharmD)
  • Track record of successful project management in the pre-clinical space with a record of successful project delivery from Candidate Selection to Regulatory Submission (IND or equivalent IMPD application), plus knowledge of the selection process of pre-clinical candidate drugs.
  • Minimum 5 years of preclinical development in pharmaceutical/biotech/CRO setting performing drug development activities such as: designing and monitoring nonclinical studies, interpreting data, generating reports and regulatory documents


Interested? Click here

Your application will be treated professionally and reservedly.

We will only reply to candidates who fulfill criteria mentioned above.