Clinical Research Nurse

Montréal, QC
On-site
Posted Oct 9, 2026
1 position

Opens an external site

Employment type: Full-time
Experience level: Entry, Junior · 0+ years
Minimum education: Professional degree
Posting language: English
Working hours: 38 hours per week

Job summary

The Clinical Research Nurse oversees participant safety and consent while ensuring compliance with study protocols and Good Clinical Practices. Responsibilities include performing safety assessments, administering investigational products, and documenting adverse events.

Job details

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 #LI-JG1

What you’ll do

Requirements

Candidates must hold a DEC from an accredited Registered Nurse program and possess a valid permit from the OIIQ. Proficiency in both English and French is required, along with strong interpersonal and communication skills.