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

• PhD in a relevant field (preferably toxicology, cancer biology, pharmacology, immunology)

• At least 3 years of industrial experience in the preclinical studies sector, incl. regulatory submission-aimed preclinical development studies

• Extensive expertise in project management of GLP / non-GLP animal experiments with rodents and non-rodents

• Knowledge of GLP regulations, including writing SOPs and study reports

• Being a team player, able to collaborate across multidisciplinary terms, and also have the ability to work independently

• Ability to work in a start-up environment

• Strong communication and interpersonal skills

• Proficient English as well as German language skills

Responsibilities

• 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

• Together with our scientists, you will design and manage in vivo studies in toxicology, pharmacology, pharmacokinetics and pharmacodynamics to meet regulatory requirements

• 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.

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WE DO LOOK FORWARD TO RECEIVE YOUR COVER LETTER AND RESUME:

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