Study Engineer - Data in Clinical Research
Siège de l'AP-HP · Public hospitals
En français : Ingénieur(e) d'études - Données en recherche clinique
This job in plain words
This job is for a study engineer based in Paris, in the digital field. The person develops and validates new methods to measure drugs by LC-MS/MS, following FDA and EMA rules.
Can you apply?
The offer does not state the contract type. A pay range is listed for contract staff, so contract staff may likely apply.
- Diploma
- Master's degree (bac+5) · Engineering degree or Master 2 in analytical chemistry, pharmaceutical sciences or an equivalent field
- Experience
- Successful experience developing and validating LC-MS/MS methods
The profile they want:
- Engineering degree or Master 2 in analytical chemistry or pharmaceutical sciences
- Experience developing and validating LC-MS/MS methods
- Good knowledge of FDA and EMA rules for bioanalysis
- Solid knowledge of pharmacokinetics
- Rigorous and independent work at the bench, with good summary skills
- Good writing skills for study documents
What you would do
- Develop and validate new drug measurement methods
- Run measurements in the lab, from sample preparation to data collection
- Help write research protocols and standard operating procedures
- Write the related study reports
How to apply
Apply on the employer's website, using the « Postuler sur le site employeur » button on the official offer page.
Good to know:
- Remote work is not stated in the offer.
We wrote this summary automatically from the official offer. Only the offer published on Choisir le Service Public counts: read it before you apply. Source: Choisir le Service Public (DGAFP), Etalab 2.0 licence.
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