Clinical Research Assistant

il y a 3 semaines


Brussels, Belgique Express Medical Temps plein

**Description**:
Vous êtes** infirmier **? Vous recherchez un n**ouveau défi et portez un intérêt à la recherche clinique** ?

**_Nous avons une opportunité pour vous _**

Express Medical recrute actuellement un **Clinical Trial Assistant.**

**Votre mission** : vous collaborez avec le Project Manager/Study Coordinator dans la réalisation des études cliniques.

**Vos principales tâches**:
Sous la supervision du Clinical Project Manager/Study Coordinator:

- vous travaillez en conformité avec les règles **GCP** (Good Clinical Practice), les **SOP **(Standard Operating Procedure), le **protocole clinique** et ses amendements ;
- vous participez à la **mise en place des études** au niveau opérationnel en collaboration avec le Project Manager/Study coordinator ;
- vous êtes l’**agent de liaison** avec l’équipe du **département clinique** ;
- vous imprimez les **résultats de biologie clinique**,** complétez les dossiers médicaux des sujets** d’étude ;
- vous participez à la **sélection des sujets d’étude**, envoyez les mails pour confirmer les RDV, assurez le suivi des visites médicales ;
- vous participez à la **conception des feuilles de travail** en vue de collecter les données des sujets d’étude ;
- vous maintenez à jour le **dossier de l’investigateur **et les documents essentiels de l’étude clinique ;
- vous participez aux **visites de monitoring** et assurez le **suivi avec le client** ;
- vous **vérifiez les données sources **et vous êtes amenés à les encoder dans l’eCRF (au besoin).

**Profil**
- vous êtes titulaire d’un **diplôme infirmier** reconnu dans l’Union européenne ;
- vous avez idéalement une première expérience en recherche clinique ;
- vous vous exprimez en** français**. Une bonne connaissance de l**'anglais **est requise (**B1 minimum)** ;
- vous avez une maîtrise de base de l’outil informatique ;
- vous êtes **dynamique et proactif** ;
- vous êtes** rigoureux et organisé**.

**Offre**
- un **contrat à durée indéterminée à temps plein** ;
- un **horaire de jour** variable entre 8:00 et 18:00 ;
- un** environnement dynamique** avec des **partenaires de renoms**,** à la pointe de la recherche pharmaceutique** ;
- des **missions variées** dans des** domaines thérapeutiques innovants** ;
- une **société à taille humaine** vous permettant de** développer vos compétences et vos initiatives.**

**Entreprise**

Notre partenaire est un **centre de recherche clinique spécialisé dans la réalisation d’essais cliniques de phase I et II.


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