Editeur/Editrice scolaire - CDD F/H AD

...scientific integrity policy) Responsibility for editorial production to press proof/digital proof stage: Working on mockups in InDesign (integrating corrections) Ensuring consistency of English and Fr...

Éditeur numérique - CDD AD

...scientific integrity policy) Responsibility for editorial production to press proof/digital proof stage: Working on mockups in InDesign (integrating corrections) Ensuring consistency of English and Fr...

CDD - Éditeur multimédia (H/F) AD

...scientific integrity policy) Responsibility for editorial production to press proof/digital proof stage: Working on mockups in InDesign (integrating corrections) Ensuring consistency of English and Fr...

Pharmacovigilance Program Director

...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

...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

...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

...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

...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

...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

...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

...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

...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

...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...

Alternant - Editeur H/F AD

...scientific integrity policy) Responsibility for editorial production to press proof/digital proof stage: Working on mockups in InDesign (integrating corrections) Ensuring consistency of English and Fr...

Alternance - Éditeur vidéo AD

...scientific integrity policy) Responsibility for editorial production to press proof/digital proof stage: Working on mockups in InDesign (integrating corrections) Ensuring consistency of English and Fr...