Senior Scientist - Mont-Saint-Guibert, België - Novadip Biosciences

Novadip Biosciences

Geverifieerd bedrijf

Mont-Saint-Guibert, België

3 dagen geleden

Geplaatst door:

Sophie Dubois

beBee Recruiter

Responsibilities:

Design and lead preclinical research and nonclinical development activities.
Design, plan and oversee in vivo pharmacology, safety and toxicology studies
Establish and manage collaborative relationships with academic partners and CROs
Responsible for developing and documenting study protocols; for data review, analyses, and interpretation; documentation and reporting of outcomes
Carry out technological and regulatory surveillance (EMA, FDA),
Project management (timelines, results, budget) : Ensure that all studies are performed in timely manner with appropriate scientific rigor and appropriate documentation.

Profile:

A PhD degree or similar experience in pharmacology, toxicology or related discipline.
At least 5 years of proven industrial experience in the nonclinical assessment of advanced therapies.
Strong understanding and broad knowledge of pharmaceutical development.
Proven track record leading nonclinical development (pharmacology, toxicology, formulation) for Biologics and/or advanced therapy medicinal products.
Demonstrated experience designing and executing a bread range of animal model studies, preferably in the field of musculoskeletal disorders.
Knowledge of GLP standards.
Teamwork and leadership experience, preferably in a biotech (startup) environment.
Flexibility to operate in multitasks environment.
Excellent organizational and communication skills.
Strong problemsolving abilities and deep commitment to excellence.
Fluent in French and English.

Offer:

A fulltime permanent position (40h/week) in a growing team.
To work in a humansized, dynamic, respectful and professional environment.
The opportunity to take part in a challenging scientific and business growth.
An attractive salary package in line with the position responsibilities and your experience.