Job Description RESEARCH INSTITUTE OF THE MUHC
Position Summary
General Duties
- Assists in the organization of research projects,
- Obtains informed consent from patients for participation in research studies,
- Interviews patients to complete study questionnaires,
- Trains patients to complete electronic study surveys,
- Performs medical chart reviews,
- Performs data entry,
- Ensures patient follow-up visits are completed,
- Organizes and maintains study documentation at various study sites,
- Accomplishes any other related tasks as required by the immediate supervisor.
Required Skills
General Skills/knowledge
- Bilingual (excellent French and English, spoken and written),
- Autonomous, flexible, sense of ethics and good judgment,
- Excellent organizational, time management skills, ability to multi-task and prioritizing time sensitive issues,
- Excellent communication and interpersonal skills.
- Excellent interpersonal skills,
- Ability to work under minimal supervision.
- Strong attention to detail,
- 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.
Status:
Pay Scale:
Work Shift:
Work Site:
If you wish to include a cover letter, please attach it with your resume in one PDF document.
- 6 days of paid sick leave per year, which includes a maximum of 3 personal day,
- Vacation calculated on a pro-rata basis based on a percentage of your salary,
- Modular group insurance plan (including gender affirmation coverage),
- RREGOP government pension plan (defined benefit plan),
- 5.3% of your gross earnings will be added to your paycheque in lieu of statutory holidays.
THIS IS NOT A HOSPITAL POSITION.
