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.

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

CIM

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 mínimal supervision,
- Quick learner, detail orientation, positive 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.

Additional information

Status : Temporary full-time (6 months replacement) Pay Scale : Commensurate with education & work experience. From $44,408.00 - $82,427.80 per year. Work Shift : 8:30 a.m. to 4:30p.m., Mondays to Fridays (35hours/week). Work Site : Glen site (1001 Décarie Blvd)

If you wish to include a cover letter, please attach it with your resume in one document.

Why work with us?

- 4-week vacation, 5th week after 5 years,
- Bank of 12 paid days (personal days and days for sickness or family obligations),
- 13 paid statutory holidays,
- Modular group insurance plan (including gender affirmation coverage),
- Telemedicine,
- RREGOP (defined benefit government pension plan),
- Training and professional development opportunities,
- Child Care Centres,
- Corporate Discounts (OPUS + Perkopolis),
- Competitive monthly parking rate,
- Employee Assistance Program,
- Recognition Program,
- Flex work options and much more!

THIS IS NOT A HOSPITAL POSITION.

**Equal Opportunity Employment Program

📌 Clinical Research Coordinator - Regulatory Affairs (Cim) (Montreal)
🏢 Centre universitaire de santé McGill - Institut de Recherche
📍 Montreal