Over the past nine years, I have acquired experience in coordination within leading pharmaceutical companies involved in international clinical trials as well as medical device company specialized into extreme orthopedic implants. Having worked under both French and UK regulatory requirements, I have the skill to adapt myself to any environment. I also have a strong experience on TMF (Paper & Electronic) and administrative follow-up.
Excellent organizational skills, very good attention to details, pro- active, flexible and able to multi-task, I’m able to work in a team and independently.
Highly motivated, I’m looking forward to be part of a CRO or a leading Pharmaceutical company to coordinate studies and liaise with the Investigators and the CRA’s in order to continually improve my competencies, my skills and knowledge in pharmaceutical regulatory and laws.