Evaluateur - Clinical Trial Methodology (Soutien
Il y a 7 mois
**L'entreprise**
**Sciensano **est l'institut créé par la fusion de l'Institut Scientifique de Santé Publique (WIV-ISP) et du Centre de Recherche Vétérinaire et Agrochimique (CODA-CERVA). Les deux instituts ont uni leurs forces pour mieux comprendre la santé des humains et des animaux. Sciensano soutient la politique de santé par le biais de recherches scientifiques innovantes, d'analyses, de surveillance et de conseils d'experts.
Plus de 850 collaborateurs participent à plus de 100 projets scientifiques financés par les autorités, des partenaires et des clients belges et internationaux. Nous contribuons de cette manière à une vie plus saine pour tous.
**Description de l'emploi**
Vous soutenez la Direction générale « PRE » de l’agence fédérale des médicaments et des produits de santé (AFMPS), qui assure le suivi du développement d’un médicament jusqu’à l’autorisation initiale de mise sur le marché.
Vous évaluez le protocole et la méthodologie des essais cliniques dans le cadre de demandes d'études cliniques, de conseils scientifiques nationaux et européens.
Vous préparez un rapport de conseils du protocole et la méthodologie de l'essai clinique.
Vous fournissez des conseils scientifiques et administratifs et défendez les différents points de vue dans le cadre de décisions stratégiques dans votre domaine d'expertise.
Vous participez également à des réunions nationales et internationales où vous défendez les positions de la Belgique.
Vous développez votre expertise dans votre domaine et la mettez au service de l’AFMPS et d’autres parties prenantes.
Vous travaillez dans un environnement dynamique et multidisciplinaire.
Votre contribution permet d’assurer la sécurité et l’efficacité des médicaments innovants.
**Le profil**
Master en sciences (bio)médicales ou bio-sciences
Expérience: min. 4 ans d'expérience pertinente dans le domaine des études cliniques (méthodologie)
Très bonne connaissance de: méthodologie des études cliniques ; obligations légales et règlements des essais cliniques ; GCP
Langues : français ou néerlandais et excellente connaissance de l’anglais (oral et écrit)
Atouts : expérience dans l’évaluation de protocoles d’études cliniques; publications dans des revues scientifiques
Compétences génériques : évaluer et prendre des décisions; influencer, négocier et convaincre; collaborer et partager ses opinions; volonté d’apprendre et esprit scientifique; planifier et organiser; gestion du stress; sens des responsabilités; orientation objectifs et clients; établir des relations et des réseaux
**L'offre**
Une fonction stimulante dans un institut scientifique renommé
Contrat de durée indéterminée
Echelle de rémunération : SW1 ou SW2
Autres : horaires de travail flexibles de 38 heures/semaine; possibilité de télétravail et de formations
**Contact**
Vous avez des questions au sujet de cette fonction ou souhaitez plus d'informations?
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