Clinical Research Coordinator - Nurse

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!

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 du poste

We are seeking a highly motivated, organized, enthusiastic and experienced individual to join our dynamic team working on novel treatments for allergy, asthma and chronic urticaria

The successful candidate must be familiar with the entire clinical trial process and be able to assume all the associated nursing tasks. The candidate will work under the direct supervision of the Project Manager and senior Study Nurse.

Principales responsabilités

• Coordination of study visits with study coordinator as per study protocol, coordinating with clinic staff to ensure proper documentation and timing of research-related procedures
• Blood collection and clinical follow-up of research participants according to the study protocol
• Timely completion of all study documentation forms, including case report forms (CRFs), adverse events reports, other study specific documents
• Review subject’s information and laboratory reports in preparation for the investigator’s review
• Performing miscellaneous job-related duties as assigned by supervisor, including support to other coordinator and research nurses
• Work directly with the Principal Investigator, the research team and collaborating laboratories/co-investigators at the study site to ensure the smooth running of all the clinical aspects of studies
• Under the supervision of the Project Manager, coordinate study activities at the study site to ensure project timelines and patient enrollment goals are achieved

Exigences

Éducation / Expérience

Education: Diploma of College Studies (DEC)
Field of Study: Nursing
Work Experience: 1+ year

Professional Membership: Good standing member of the OIIQ

Compétences requises

REQUIREMENTS:

Education, Experience and Knowledge

• Nursing DEC is required, Bachelor's degree is an asset,
• Good standing member of the OIIQ,
• Relevant experience in clinical research is an asset,
• Bilingual: French and English spoken and written,
• Solid written and verbal communication skills,
• Strong proficiency in Microsoft Office programs (Word, Excel, PowerPoint) and Web applications.

Skills

• High level of initiative and organization,
• Ability to prioritize and to multitask,
• Willingness to learn and adapt to new situations,
• Demonstrated ability to work independently as well as within a team,
• Strong critical and clinical thinking.