Détails du poste
- Lieu de travail : Montreal
- Type de poste : Permanent à temps plein
Description du poste
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!
Description de l’organisation
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).
Résumé de poste
Position summary
Department / Research Program: Cardiac Electrophysiology - Cardiovascular Health Across the Lifespan Program (CHAL)
Under the supervision of the manager of the Clinical Research Unit in cardiac electrophysiology and the Principle Investigator
Investigator, the incumbent will be responsible for supporting the successful conduct of clinical research studies.
Tâches générales
- Assists in the planning/organization of research projects
- Recruitment of studyparticipants (Identify and screen potential subjects, obtain informed consent)
- Coordination of study visits as per study protocol
- Execution of all aspects of study visit (adverse events, safety, questionnaires, sample collection including processing and shipment of samples according to clinical protocol)
- Clinical evaluation of subjects according to protocol requirements
- Provide coordination and timely completion of all aspects of data collection and sources documentation
- Timely completion of electronic CRFs as for clinical trial requirements
- Respond promptly to queries and requests for information
- Conduct other related tasks as assigned by supervisor
Site web de l’organisation
Éducation / Expérience
- Education: Bachelor's Degree
Field of Study: Science - Work Experience: Minimum of one (1) year experience in clinical research
Compétences requises
- 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 patients who are exclusively proficient in English. The position also requires complex writing or in-depth analysis of documents in English related to a research project.
- Autonomous, flexible, sense of ethics and good judgment,
- Excellent organizational, time management skills, ability to multi-task and prioritizing time sensitive issues,
- Excellent interpersonal skills,
- Ability to work under minimal supervision,
- Ability to generate and maintain accurate records,
- Strong analytical and problem solving skills,
- Decision making:
- Planning, implementing and evaluating patient care.
- While the investigator is the main responsible for his/her study, the incumbent must ensure protocol compliance including participant eligibility.
- Clinical research experience is an asset.
