- Location
- Site Montreal - 1200 Beaumont, Canada · West Island, Montreal · Laval, Quebec
- Workplace
- Onsite
- Type
- Full-time
- Department
- Healthcare
- Source
- Workday
Description
About The Role
The Clinical Research Nurse will oversee the safety and consent of clinical trial participants during study conduct and the maintenance of safety equipment. The Clinical Research Nurse will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).
What You'll Do Here
Perform scheduled inspection of emergency crash carts, inventory/inspect the contents, and maintain up to date records.
Ensure the confidentiality of clinical trial participants and sponsors is respected.
Perform clinical trial activities including but not limited to, continuous safety monitoring, safety assessments, Investigational Product (IP) administration and catheter installation.
Monitor, document and/or follow-up on participant adverse events.
Maintain and advocate a high level of patient care, quality, and safety within the department.
May assist in study related consenting with participant screenings.
Provide feedback, where necessary, to appropriate team members of study progress.
Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
May train employees on clinical trial activities associated to their job’s needs.
Other tasks as assigned by management.
What You'll Need to Succeed
DEC from accredited Registered Nurse program required
Permit from the Ordre des infirmiers et infirmières du Québec (OIIQ) required.
Good communication in French and English.
Customer service focused.
Able to work in fast-paced environment.
Knowledge of the Microsoft suite
Excellent verbal and written communication skills.
Well-developed interpersonal skills are required.
Personal/professional integrity and proven discretion in handling confidential information.
Capable of managing multiple conflicting priorities.
Relevant industry experience a plus.
Altasciences strives to provide a French working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the above-mentioned requirement. Fluency in English is an essential requirement for the position of Clinical Research Nurse including, but not limited to, for the following reasons:
The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.
What We Offer
Full time position (37,5 hours/week).
Availability every other weekend is required.
Day, evening or night shift (no shift rotation).
6 to 8 weeks of theory and practical training on the day shift.
On site position at our Montreal site (1200 Beaumont).
Accessible by public transportation (Metro L' Acadie), Free parking for employees.
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences’ Benefits Package Includes:
Health/Dental/Vision Insurance Plans
RRSP with Employer Match
Paid Vacation and Holidays
Paid Sick and Bereavement Leave
Employee Assistance & Telehealth Programs
Altasciences’ Incentive Programs Include:
Training & Development Programs
Employee Referral Bonus Program
Annual Performance Reviews
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