This WEB site is dedicated to my (Pierre LECOCQ) professionnal activities.
Most Recent Modifications.
As a result of my course (Clinet/CEFOCHIM) for "Expertise in Clinical Research" and an internship at Artialis S.A., I can now provide you with consultancy/support as e.g. Data Manager, Biostatistician, Medical Writer or CTA in your clinical research activities.
See my most recent Competencies' file: Click Here
Or for more details my Resume: Click Here
What I am interested in (or not).
Definitively NOT in Regulatory, QA and QC. The main reason is that these matters should be handled internally. Who is best placed than developpers to carry out validation of their research? They do not about regulation ongoing? Peanuts! This can be found on the WEB. But their in deep knowledge of the service/product who externally can carry over with this?
So being more positive:
1. Next Generation Sequencing applied in Health Care / Diagnostics.
2. Biostats and Data Management in Clinical Research.