We are currently looking for a Preclinical Research Associate to design and conduct preclinical studies involving wearable and implantable medical devices.
Join an independent, innovative and fast-growing company for the research and development of class III Medical Devices.
Be part of a growing international team of scientists, clinicians and engineers working to better understand the brain and neurosciences to improve lives !
Design and conduct non-clinical trials (bench and in vivo) that involve advanced wearable and implantable technologies developed within the company
Perform routine non-clinical procedures and measurements, and record research data according to study protocols
Develop experimental methods and study protocols in accordance with Good Laboratory Practices (GLP) and Standard Operating Procedures (SOP) and practices
Perform pre-clinical study preparation activities including experimental room set-up and equipment calibration
Utilize and enhance automated data analysis tools for inspection, post-processing and data modeling
Communicate methods and results within the company and to project collaborators
Keep abreast of scientific trends, innovations, and the scientific literature
Critically appraise and contribute to the development of recommendations for the design of evidence-based experiments
Your Profile :
MSc in Neuroscience or in Biology or a related discipline such as systems neuroscience, behavioral neuroscience, with a solid background in data acquisition devices used in electrophysiology or other modalities
At least 5 years (BS) or 3 year (MS) of work experience in an industrial or academic setting
Strong experience with non-clinical study design, protocol writing and execution preferably with emphasis on large models – Laboratory training (LTK Module 1, 20 or equivalent)
Experience with data analysis methods, including close familiarity with a programming language such as Python and MATLAB
Experience in scientific reporting (writing research articles, R&D reports etc)
Experience in non-clinical studies for medical devices or in-vitro diagnosis medical devices is a plus
Familiar with quality assurance procedures and international standards is a plus
Fluent in English ; French is a plus
For more information, feel free to contact Morgane CAYUELA at firstname.lastname@example.org
Recruitment Specialist Life Sciences
Team Leader & Recruitment Management Life Sciences