- Pharmiweb
- Nouvelle-Aquitaine
- Scientific
- 1 heure il y a
- Favoris
- plus...
...quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile:: Bachelor's degree in a scientific or healthcare-...
- Pharmiweb
- Île-de-France
- 1 heure il y a
- Favoris
- plus...
...quality of study conduct. You are: Bachelor’s Degree (or equivalent) with 2-4 years of relevant healthcare experience in the pharma or clinical research industry. Minimum 2 years of monitoring and sit...
- Pharmiweb
- Île-de-France
- Administration
- 1 heure il y a
- Favoris
- plus...
...quality and consistency of interventional study deliverables to time, cost and quality objectives. As aClinical Trial Assistantyou will have the opportunity to experience the full lifecycle of a proje...
- Pharmiweb
- Nouvelle-Aquitaine
- Scientific
- 1 heure il y a
- Favoris
- plus...
...quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile:: Bachelor's degree in a scientific or healthcare-...
- Pharmiweb
- Île-de-France
- 1 heure il y a
- Favoris
- plus...
...quality of study conduct. You are: Bachelor’s Degree (or equivalent) with 2-4 years of relevant healthcare experience in the pharma or clinical research industry. Minimum 2 years of monitoring and sit...
- Pharmiweb
- Île-de-France
- Administration
- 1 heure il y a
- Favoris
- plus...
...quality and consistency of interventional study deliverables to time, cost and quality objectives. As aClinical Trial Assistantyou will have the opportunity to experience the full lifecycle of a proje...
- Pharmiweb
- Île-de-France
- Scientific
- 1 heure il y a
- Favoris
- plus...
...quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile:: Bachelor's degree in a scientific or healthcare-...
- Pharmiweb
- Nouvelle-Aquitaine
- Administration
- 1 heure il y a
- Favoris
- plus...
...quality and consistency of interventional study deliverables to time, cost and quality objectives. As aClinical Trial Assistantyou will have the opportunity to experience the full lifecycle of a proje...
- Pharmiweb
- Île-de-France
- 1 heure il y a
- Favoris
- plus...
...quality of study conduct. You are: Bachelor’s Degree (or equivalent) with 2-4 years of relevant healthcare experience in the pharma or clinical research industry. Minimum 2 years of monitoring and sit...
- Pharmiweb
- Pays de la Loire
- 1 heure il y a
- Favoris
- plus...
...quality of study conduct. You are: Bachelor’s Degree (or equivalent) with 2-4 years of relevant healthcare experience in the pharma or clinical research industry. Minimum 2 years of monitoring and sit...
- Pharmiweb
- Grand Est
- Scientific
- 1 heure il y a
- Favoris
- plus...
...quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile:: Bachelor's degree in a scientific or healthcare-...
- Pharmiweb
- Grand Est
- Administration
- 1 heure il y a
- Favoris
- plus...
...quality and consistency of interventional study deliverables to time, cost and quality objectives. As aClinical Trial Assistantyou will have the opportunity to experience the full lifecycle of a proje...
- Pharmiweb
- Hauts-de-France
- Administration
- 1 heure il y a
- Favoris
- plus...
...quality and consistency of interventional study deliverables to time, cost and quality objectives. As aClinical Trial Assistantyou will have the opportunity to experience the full lifecycle of a proje...
- Pharmiweb
- Île-de-France
- Scientific
- 1 heure il y a
- Favoris
- plus...
...quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile:: Bachelor's degree in a scientific or healthcare-...
- Pharmiweb
- Nouvelle-Aquitaine
- Administration
- 1 heure il y a
- Favoris
- plus...
...quality and consistency of interventional study deliverables to time, cost and quality objectives. As aClinical Trial Assistantyou will have the opportunity to experience the full lifecycle of a proje...