Clinical Research Assistant
Il y a 6 mois
**Description**:
Vous êtes** infirmier (h/f/x) **? 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) ;
- vous pouvez être amené à r**enforcer l'équipe de terrain** (suivi des sujets volontaires, **prise des paramètres, ECG, injections, administration de vaccins,...)**, l'**équipe de recrutement, **ou encore** l'équipe qualité.**
**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 de longue durée (4 à 5 mois) à plein temps **;
- un **horaire de jour du lundi au vendredi,** variable entre 8:00 et 18:00 ( essentiellement 08h-16h);
- 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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