Ms. Nelle Stocquart
Trainer
With a master’s in chemistry Nelle Stocquart works since 2003 in the Clinical Research world. She was first an IVRS project manager for a Belgian CRO but then she wished gaining more experience on the field and became CRA for a top 5 international CRO where she got involved in many international phases II & III from early study stage till closure. She then evolved as project manager in pharmaceutical companies and CRO where she managed local and international studies from phase I to phase IV. She is now working for the Belgian government which is funding academic studies.
Nelle has a lot of experience in project management, team management and people coaching. Training, Coaching, Education and Continuous Professional Development have always been the common pillars in her educational path and professional career. She speaks fluently 3 languages (Dutch, French and English).
Her real passions are “technical skills”-trainings:
- Project Management
- Risk Management
- Risk-Based Monitoring
- MS Project
- Time Management
- GCP trainings
- Etc.
She is providing open courses, but also tailor-made sessions adapted to the specific needs of the customer.
LinkedIn Profile
This 4 Day STAR Programme is intended for CRAs, ambitious to further develop their career as a CRA. ...
Reasons to attend How to ensure a successful clinical trial within timelines and budget? This C...
This programme, consisting of five-course days to be chosen freely from the available dates in the p...
Reasons to attend Whether or not you want to outsource specific activities or your entire trial, yo...
Back on September 27th, we organised our first free webinar on How to reduce time between site ...
Reasons to attend You want to know where investigational products come from, how they are made an...
Reasons to attend You need to update and refresh your knowledge on ICH-GCP, including the ICH-GCP E...
Reasons to attend You need to update and refresh your knowledge on ICH-GCP, including the ICH-GCP E...
Reasons to attend You are new to the industry and need to know the basics? You would like to know m...
Reasons to attend Investigator Initiated Studies (IIS) are crucial for new product development. The...
Do you need straightforward instructions on how to write an effective CAPA? Looking for a brief ex...
Reasons to attend This series of webinars will provide hands-on tips how to use MS Project in an ef...
Reasons to attend Risk Based Monitoring is a hot topic nowadays. It must be implemented in your org...
Reasons to attend You want to know the ins and outs of risk management in clinical research? You wa...