Responsable de marché médical F/H

Directeur/Directrice médical(e), premières phases - Poste basé dans la ville de Québec
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Why Syneos Health
technical and therapeutic area training; We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

En tant que membre de l’équipe Syneos Health, vous participerez à l’obtention de résultats dans un objectif plus que valorisant : améliorer la vie de patients partout dans le monde. Nous apprécions votre engagement envers nos clients et nos patients, nous voulons donc nous engager envers vous en vous offrant un programme d’avantages sociaux complet comprenant une couverture pour tous les aspects médicaux, physiques, psychologiques et financiers.
• En collaboration avec l’équipe médicale et de sécurité clinique, a ssurer en tout temps la sécurité des participants pendant l’étude clinique ainsi qu’après la fin de l’étude, conformément au protocole et aux règles de Bonnes pratiques cliniques (GCP).

• ​ Planifier et réaliser l’ensemble des activités médicales liées à l’admissibilité des participants (examen médical, résultats de laboratoire, interprétation d’électrocardiogrammes, etc.) afin de garantir le respect des critères d’inclusion et d’exclusion.
• ​ Évaluer les e ffets indésirables et porter les jugements médicaux appropriés; Examiner les protocoles et les formulaires de consentement éclairé afin de garantir la sécurité des participants et l’intégrité des données.
• ​ S’assurer que l’équipe médicale est qualifiée, formée et dûment déléguée pour les séances de sélection et pour l’étude.
• ​ Planifier, organiser, gérer et suivre les activités médicales à l’Unité de recherche clinique de Québec selon les besoins opérationnels de l’organisation.
• ​ Superviser, encadrer et agir comme mentor auprès de l’équipe médicale et du personnel clinique.
• ​ Peut se voir attribuer d’autres tâches cliniques.

• Doctorat en médecine .
• ​ Maîtrise du français; bonne compréhension de l’anglais.
• ​ De cinq à huit ans d’expérience en pratique médicale; expérience en recherche clinique considérée comme un atout.
• ​ Compréhension et connaissance de l’industrie pharmaceutique et des organisations de recherche sous contrat en général, ainsi que du milieu clinique.
• ​ De plus, rien dans la présente ne doit être interprété comme créant un contrat de travail. Get to know Syneos Health

Learn more about Syneos Health.

Further, nothing contained herein should be construed to create an employment contract. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
In collaboration with the management team, the medical director oversees all medical services occurring at our Quebec City Clinical Research Unit. In addition, being also a Clinical Investigator, he/she is responsible for all medical activities related to clinical trials, data integrity, and safety of participants.
Along with the medical and safety team, ensure subject safety at all times during the clinical study and after the study has been completed as required by the protocol and Good Clinical Practice regulations.

• Plan and carry out the full spectrum of medical activities related to subject eligibility for studies (e.g., medical exam, laboratory results, electrocardiogram assessment, etc) so that inclusion and exclusion criteria are adhered to.
• Assess adverse events and make an appropriate medical judgement; Review protocols and informed consent forms to ensure participant safety and data integrity
• Ensure that the medical team is qualified, trained, and delegated for screening sessions and for the study.
• Plan, organize, manage, and monitor medical activities at the Quebec City Clinical Research Unit according to the operational needs of the organization.
• Supervise, coach, and mentor medical team and clinical staff
• Doctorate in medicine
• Fluency in French, Proficiency in English
• Five to 8 years of medical practice, and experience in clinical research considered an asset
• Knowledge of GCP/ICH guidelines and other applicable regulatory requirement considered an asset.
• Understanding and knowledge of the pharmaceutical industry and contract research organizations in general, and the clinical community specifically.