- ProductLife Group
- Auvergne-Rhône-Alpes
- 3 jours il y a
- Favoris
- plus...
...scientific backgroundMinimum 5-10 years experience working for service providersPharmaceutical background – strong understanding of GVP, GCP, FDA and regulatory requirements related to drug safety.Dee...
- ProductLife Group
- Bretagne
- 3 jours il y a
- Favoris
- plus...
...scientific backgroundMinimum 5-10 years experience working for service providersPharmaceutical background – strong understanding of GVP, GCP, FDA and regulatory requirements related to drug safety.Dee...
- ProductLife Group
- Centre-Val de Loire
- 3 jours il y a
- Favoris
- plus...
...scientific backgroundMinimum 5-10 years experience working for service providersPharmaceutical background – strong understanding of GVP, GCP, FDA and regulatory requirements related to drug safety.Dee...
- AIXIAL GROUP
- Auvergne-Rhône-Alpes
- 1 semaine il y a
- Favoris
- plus...
...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...
- AIXIAL GROUP
- Centre-Val de Loire
- 1 semaine il y a
- Favoris
- plus...
...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...
- AIXIAL GROUP
- Bourgogne-Franche-Comté
- 1 semaine il y a
- Favoris
- plus...
...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...
- AIXIAL GROUP
- Auvergne-Rhône-Alpes
- 1 semaine il y a
- Favoris
- plus...
...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...
- AIXIAL GROUP
- Provence-Alpes-Côte d'Azur
- 1 semaine il y a
- Favoris
- plus...
...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...
- AIXIAL GROUP
- Provence-Alpes-Côte d'Azur
- 1 semaine il y a
- Favoris
- plus...
...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...
- AIXIAL GROUP
- Grand Est
- 1 semaine il y a
- Favoris
- plus...
...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...
- AIXIAL GROUP
- Occitanie
- 1 semaine il y a
- Favoris
- plus...
...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...
- AIXIAL GROUP
- Bretagne
- 1 semaine il y a
- Favoris
- plus...
...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...
- AIXIAL GROUP
- Île-de-France
- 1 semaine il y a
- Favoris
- plus...
...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...
- ProductLife Group
- Grand Est
- 3 jours il y a
- Favoris
- plus...
...scientific backgroundMinimum 5-10 years experience working for service providersPharmaceutical background – strong understanding of GVP, GCP, FDA and regulatory requirements related to drug safety.Dee...
- ProductLife Group
- Pays de la Loire
- 3 jours il y a
- Favoris
- plus...
...scientific backgroundMinimum 5-10 years experience working for service providersPharmaceutical background – strong understanding of GVP, GCP, FDA and regulatory requirements related to drug safety.Dee...