Clinical Research Coordinator - CIM

Research Institute of the McGill University Health Centre

Montreal
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Détails du poste

  • Lieu de travail : Montreal
  • Type de poste : Permanent à temps plein

Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the McGill University Health Centre (RI-MUHC), you can be part of an organization focused on scientific discovery and innovation in patient-centered medicine. Join us today and make a difference!

Job Description

RESEARCH INSTITUTE OF THE MUHC
The Research Institute of the McGill University Health Centre (RI-MUHC) is a world-renowned biomedical and hospital research centre. Located in Montreal, Quebec, the Institute is the research arm of the McGill University Health Centre (MUHC) affiliated with the Faculty of Medicine at McGill University. The RI-MUHC is supported in part by the Fonds de recherche du Québec - Santé (FRQS).

Position summary
Under the supervision of the Manager, Clinical Research Administration Centre for Innovative Medicine (CIM), the incumbent is responsible for supporting the submission of clinical research studies to the Centre of Applied Ethics and other site specific assessment.

General Duties
• Review and revise sponsor’s informed consent forms so that it meets FRSQ standard approved language,
• Work with sponsors and study teams to obtain all documents required to start submissions,
• Submit studies through Nagano to reviewing committees (ethics and site specific reviews),
• Maintain on going communication with Ethics, Contracts, Investigators, and Sponsors during submission and renewal timelines to ensure that all needs are meet met,
• Optimize study review time,
• Primary point of contact for all stakeholders,
• Conduct other related tasks as assigned by supervisor.

Website of the organization

Education / Experience

Education: Diploma of College Studies (DEC)
Field of study: Science

Work experience: Minimum 1 year of experience in ethics and/or regulatory submissions is a definite asset. Knowledge of clinical research.

Required Skills

• Advanced knowledge of oral and written French is required,
• An advanced knowledge of oral and written English is required, as the position requires regular and complex contact with researchers or international students who are exclusively proficient in English,
• Able to multi-task and prioritize workload,
• Organized,
• Solid written and verbal communication skills,
• Able to work under minimal supervision,
• Quick learner, detail orientation, good adaptability and versatile,
• Excellent knowledge of computer skills, as well as Word, Excel and PowerPoint,
• Knowledge of Nagano systems an asset, and
• Self-directed, organized and sense of ethics.