FEB 2021
- WE - ARE - HIRING -
Fullspeed towards clinical phase I
Our lead drug ALBUPLATIN is in the last exciting third of its preclinical development.
For our final boost we are now seeking a highly qualified
PRECLINICAL DEVELOPMENT COORDINATOR (Part-time)
Key Qualifications
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PhD in a relevant field (preferably toxicology, cancer biology, pharmacology, immunology)
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At least 3 years of industrial experience in the preclinical studies sector, incl. regulatory submission-aimed preclinical development studies
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Extensive expertise in project management of GLP / non-GLP animal experiments with rodents and non-rodents
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Knowledge of GLP regulations, including writing SOPs and study reports
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Being a team player, able to collaborate across multidisciplinary terms, and also have the ability to work independently
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Ability to work in a start-up environment
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Strong communication and interpersonal skills
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Proficient English as well as German language skills
Responsibilities
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You are the interface between responsible authorities, ethics committees and scientists responsible to respond to health authority questions, coordinate and prepare all relevant documentation for pre-IND and IND submissions
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Together with our scientists, you will design and manage in vivo studies in toxicology, pharmacology, pharmacokinetics and pharmacodynamics to meet regulatory requirements
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Being involved in analysing and interpreting data and ensure compliances with GLP regulations in designing protocols
Remuneration
For this PART-TIME position we offer an annual gross salary of min. EUR 35.000,-, based on your qualifications and experience.