Pharmacovigilance Program Director AD

...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...

Pharmacovigilance Program Director AD

...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...

Pharmacovigilance Program Director AD

...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...

Pharmacoepidemiologist M/F

...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...

Pharmacoepidemiologist M/F

...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...

Pharmacoepidemiologist M/F

...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...

Pharmacoepidemiologist M/F

...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...

Pharmacoepidemiologist M/F

...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...

Pharmacoepidemiologist M/F

...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...

Pharmacoepidemiologist M/F

...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...

Pharmacoepidemiologist M/F

...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...

Pharmacoepidemiologist M/F

...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...

Pharmacoepidemiologist M/F

...scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)Ensuring the operational follow-up of entrusted ...

Pharmacovigilance Program Director AD

...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...

Responsable d'un Site de Production Industrielle AD

...Scientific est un réseau international de laboratoires comptant prés de 64000 collaborateurs opérant dans le domaine des sciences de la vie, proposant une gamme unique de services d’analyse à des clie...