Cantrain’s Institutional Clinical Research

2 months 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
CANTRAIN is a national clinical trial training program (CTTP) in response to a call by the Canadian Institutes for Health Research (CIHR). Its vision is to offer the best, certified and standardized clinical trials’ training and mentoring program across Canada accompanied by Internships for Trainees in a real-world setting.

General Duties
The CRE uses adult learning principles and instructional strategies to adapt, deliver, and evaluate CANTRAIN educational programs to enhance and promote clinical research competency, achieve high standards of regulatory compliance and facilitate clinical research professional development activities.

The CRE is responsible for the on-boarding and ongoing education of clinical research staff, students and clinician researchers, from novice to expert abilities, using the CANTRAIN clinical trial training streams learning pathways. Educational programming is expected to be variable in delivery mode and style, and sensitive to the role complexities found in a research hospital.

The role requires well-developed communication skills (written and oral) and advanced clinical research skills.
Website of the organization

Education / Experience

**Education**: Bachelor's Degree

**Field of Study**: Advanced training in adult education or commensurate experience preferred.

**Work Experience**: Experience in education/teaching required, including experience developing, implementing, presenting, and evaluating educational programs, either in an educational setting or in a hospital strongly preferred,
Five to seven years of clinical research experience within a university, research institute, or hospital research environment, Experience coordinating or managing clinical trials.

**Professional Membership**: ? Yes ? No

**Other requirements**:
? Knowledge of guidelines and regulations governing clinical research, Certificate demonstrating competency in Tri-Council Policy Statement (TCPS2): Ethical Conduct for Research Involving Humans and International Conference on Harmonization - Good Clinical Practice (ICH-GCP),
? Current Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals certification (ACRP) is preferred,
? Working proficiency in both English and French (where necessary),
? Excellent presentation, interpersonal and communication skills,
? Customer service oriented with the ability to work well under pressure,
? Strong problem-solving skills,
? Ability to work with mínimal supervision, take initiative and make independent decisions,
? Strong attention to detail and accuracy, excellent organizational skills with ability to prioritize, coordinate and simultaneously maintain multiple assignments with high level of quality and productivity,
? Ability and willingness to travel within Canada at least once per year to a maximum of 5 business days,
Additional information

**Status**: Temporary Full-Time (35-hour workweek) 3-year term

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

**Work Shift**: 8:30 am to 4:30 pm

**Work Site**: 5252 de Maisonneuve

**If other, please specify**: Hybrid, 2-days in-person and 3-days teleworking

THIS IS NOT A HOSPITAL POSITION.
Equal Opportunity Employment Program

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