Planning and conducting pre-clinical experiments.
Develop pre-clinical strategy for innovative high risk medical device (FDA and EU regulatory submission)
Submission of ethical requests.
Conducting comprehensive literature reviews.
Preparation of preclinical documents (e.g. protocols, reports, CRFs).
Documentation of preclinical experiments and processing the preclinical data.
Close contact with external consultants and Contract Research Organizations (CROs), both locally and internationally.
Experience in animal testing
Experience in pre-clinical development of pharmaceutical products - advantage
Preferably 4 years' experience
An academic degree in life science or medicine fields (veterinary, biology, biomedical engineering, biotechnology, biochemistry, medicine etc.)