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Clinical Trial Liaison

5 months ago

Montréal, Canada Syneos Health Commercial Solutions Full time

**Overview**

**Vous êtes un expert extraverti, à la fois chercheur et communicatif, scientifique et social.**

S'il y a une chose que votre préparation à l'obtention de votre diplôme d'études supérieures vous a apprise, c'est comment faire évoluer votre expertise rapidement et rester à l'avant-garde de votre domaine. Forger de nouvelles relations et établir des liens avec des leaders d'opinion vous vient naturellement et vous aimez être entouré de gens. Posé et éloquent, vous êtes une personne à l'écoute, un éducateur et un cultivateur doué de possibilités nouvelles et passionnantes fondées sur la science. Vous avez ce qu'il faut pour être un agent de liaison des essais cliniques avec **Syneos Health.**

**Responsibilities**

L'agent de liaison des essais cliniques établira, cultivera et entretiendra des relations scientifiques avec les chercheurs et les coordonnateurs de l'étude pour soutenir l'inscription tout en développant une solide compréhension de la pratique clinique en ce qui concerne les domaines d'intérêt. Le (la) titulaire de ce poste interagit avec divers intervenants internes et externes, en mettant l'accent sur les établissements et leurs partenaires d'alliance (le cas échéant), les coordonnateurs de l'étude, les pharmaciens, les associés de recherche clinique et les chercheurs. Ce rôle se concentrera initialement sur les essais cliniques et l'engagement du centre d'étude, mais pourrait plus tard avoir l'occasion de passer à un rôle traditionnel d'agent de liaison médicale et scientifique.
- Établir et entretenir de solides relations de travail avec les chercheurs principaux (CP), les coordonnateurs de l'étude et les centres d'essais cliniques pour soutenir l'inscription et la réalisation des études cliniques des clients
- Travailler avec les responsables du développement clinique et des opérations cliniques des clients et des ORC et les centres d'essai pour comprendre et mettre en œuvre efficacement les protocoles d'étude
- Collaborer avec les centres pour élaborer et mettre en œuvre des stratégies locales et régionales efficaces de recrutements de sujets, suggérer des options de sensibilisation locales, faciliter transmission à l'échelon supérieur des questions et des préoccupations des chercheurs, des initiatives de recrutement ou de rétention et des réunions des centres cliniques et des chercheurs en ce qui concerne les stratégies de recrutement
- Faire le suivi auprès des centres après la VSI pour s'assurer que l'inscription des patients se déroule sans heurts, déterminer les défis, les problèmes et les obstacles et signaler au client et travailler avec le personnel de l'étude et les centres pour élaborer des solutions
- Fournir une formation médicale et scientifique, au besoin, aux centres d'essai et fournir des commentaires aux principaux intervenants internes sur le matériel de formation pour les essais cliniques, les ressources expérimentales, les domaines thérapeutiques et l'état de la maladie; suggérer et soutenir la mise en œuvre d'options de sensibilisation locales
- Recueillir et partager les « pratiques exemplaires » et les tactiques pour l'inscription rapide des patients parmi les centres d'essai
- Recueillir des données et de l'information sur les principaux indicateurs des défis et des réussites du site et transmettre les données à l'équipe
- Au besoin, élaborer un réseau et des cartes de densité des professionnels de la santé et des hôpitaux participant au diagnostic et à la prise en charge des patients propres à l'étude
- Communiquer les demandes du chercheur ou coordonnateur de l'étude nécessitant un suivi auprès des personnes-ressources désignées et collaborer avec les équipes cliniques avant de fournir des réponses approuvées aux demandes du centre de manière appropriée pour assurer que les renseignements cliniques et scientifiques sont ciblés et équilibrés
- Le rôle de l'agent de liaison des essais cliniques peut offrir l'occasion de passer à un rôle traditionnel d'agent de liaison médicale et scientifique, y compris l'identification, la cartographie et l'engagement des leaders d'opinion clés; l'éducation sur l'état de la maladie et FXI/FXIa; la collecte de renseignements médicaux; l'évaluation du diagnostic des patients, des cheminements de soins et des modèles d'orientation; l'organisation de réunions de comités consultatifs et de groupes de discussion

**Job Requirements**
- IA, B.S.N., NSM, PN, PA, PharmD, Ph. D. ou MD avec expérience pertinente au centre d'essai clinique
- Expérience dans le domaine cardiovasculaire requise; expérience en oncologie, un atout important. Expérience de travail avec des agents injectables, un atout
- Connaissance de la conception et de la conduite d'essais et de recherches cliniques dans le domaine cardiovasculaire, et compréhension des résultats des études cliniques.
- Expérience en recherche clinique, en inscrip