Véronique Jobert

Involved in clinical research operations for more than 15 years in Big Pharma or Biotech companies, I would be happy to support you in your clinical projects!

I am very flexible and can adapt to different types of environment.

I have a very good contact and team spirit and I like to work in international and multicultural teams. native French and good English speaker.

I can support you in study set up and follow up of your project from start to finish and coordinate a study team and activities such as protocol design, study set-up, CRO selection and oversight, vendor contract, budget, timelines, methodology, site selection, regulatory submission follow-up, safety monitoring, reporting and follow-up, protocol deviation follow-up, data management and validation, CAPA, quality, ...

Most important: Quality/Timelines/Budget... and team spirit.

Do not hesitate to contact me...