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 ...

Senior Clinical Scientist (Senior Director) – Oncology ...

...scientific conferencesWhat We’re Looking For:Medical Doctor (MD) with a strong scientific background10+ years of experience in oncology drug development, from pre-clinical through to registrationDemon...

Senior Clinical Scientist (Senior Director) – Oncology ...

...scientific conferencesWhat We’re Looking For:Medical Doctor (MD) with a strong scientific background10+ years of experience in oncology drug development, from pre-clinical through to registrationDemon...

AFM Applications Scientist

...scientific matters – e.g. fielding technical questions from prospective customers, interpreting technical claims by competitors, contributing to marketing materials, educating non-technical staff on n...

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...