Cecile Delahaye

Pharmaeutical Professional with more than 15 years experience in clinical trials in both the pharmaceutical and medical device industry.

In this position I was responsible for a number of research projects on pain and gynaecology in The Netherlands. Grunenthal B.V. was established in The Netherlands in 2001. The company has a small medical department, which offered me the opportunity to supervise studies from start to finish, giving the job a very broad quality.

At CTO B.V I was involved in varied activities, characteristic for a young start-up company. I had the opportunity to work for many different costumers in both the pharmaceutical and medical device industries. I also acquired a lot of international experience in this period. Duties included: drafting proposals, account management, monitoring and project management of several international clinical trials with sites in the UK, Italy, Belgium, Germany and Switzerland. Monitoring of phase I studies.

As CRA, and later Lead CRA at Chiron I was involved in two multi-national vaccine studies that took place in the UK. Duties included training of local teams in the UK, co-organising study meetings, co-managing of local CRAs, co-monitoring and general project management.

Coordination and monitoring a urology study in six centers (The Netherlands and Belgium).

Small sales organisation in The Netherlands with its head offcice in Oslo. I was the only person at the Medical Department there and was involved in many local studies, later also international multicenter studies. Duties included setting up and supervising local investigator-initiated studies, writing protocols, writing study reports, coordinate regulatory affairs activities, pharmacovigilance and recall procedures.

Medical Biology Haematology