Clinical Trial Monitor

2 weeks ago

Montréal, Canada Centre universitaire de santé McGill Full time

Organization description

Le Centre universitaire de santé McGill (CUSM) est un centre hospitalier universitaire intégré, reconnu à l’échelle internationale pour l’excellence de ses programmes cliniques, de sa recherche et de son enseignement. Le CUSM a pour objectif d’assurer aux patients des soins fondés sur les connaissances les plus avancées dans le domaine de la santé et de contribuer au progrès des connaissances.
**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
We are seeking to appoint a Clinical Trial Monitor to provide monitoring, operational, and administrative support for a large international study based at the Research Institute of the McGill University Health Centre (RI-MUHC).

The Staphylococcus aureus Network Adaptive Platform (SNAP) trial aims to determine the best combination of treatment options for patients with golden staph bloodstream infections. SNAP will recruit patients from Canada, Australia, New Zealand, Singapore, Israel, and the United Kingdom.

General Duties

The Clinical Trial Monitor will report directly to Dr. Matthew Cheng, Dr. Todd Lee, and the SNAP Clinical Trial Manager for Canada.
Website of the organization

Education / Experience

**Education**: Bachelor's Degree

**Field of Study**: in science, health science, biomedical science or nursing or in progress towards and relevant experience or an equivalent combination of relevant experience and/or education/training.

**Work Experience**: Experience of clinical trial monitoring and an understanding of trial regulatory related issues.

**Other requirements**:

- Excellent English competency, spoken and written,
- Good French competency, spoken and written,
- Ability to work independently or with teams with minimum supervision,
- Strong knowledge of clinical trial regulations and related compliance systems,
- Excellent organizational and administrative skills with the ability to work with a high level of attention to detail in relation to monitoring, preparation of documentation, compliance, and reporting requirements,
- Excellent interpersonal, written, and verbal communication skills to support group interaction, including preparation of monitoring reports, plans, and organization of meetings with site staff,
- Ability to offer advice and support on trial monitoring,
- Knowledge of Microsoft Office (Word, Excel, Power Point and Outlook),
- Ability to adapt to evolving project demands and demonstrate flexibility of approach to achieve objectives,
- GCP certification (or the commitment to obtain it prior to beginning in the position),

Additional information

**Status**: Temporary Full-Time (35-hour workweek)
28-35 hours/week

**Pay Scale**: Commensurate with education and experience

**Work Shift**: Monday through Friday, start and end time flexible

**Work Site**: Glen

**If other, please specify**: Remote work possible

THIS IS NOT A HOSPITAL POSITION.
Equal Opportunity Employment Program

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