Clinical Research Nurse

at  Altasciences

Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you’re a recent college graduate or seeking your next career opportunity, it’s time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
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 in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.

What You’ll Do Here

• Perform scheduled inspection of emergency crash carts, inventory/inspect the contents, and maintain up to date records.
• Act as a mentor to Clinical Operations team members.
• Ensure the confidentiality of clinical trial participants and sponsors is respected.
• Continuously assess safety improvement opportunities and communicate with departmental management.
• Perform clinical trial activities including but not limited to, continuous monitoring, safety assessments, Investigational Product (IP) administration and catheter installation.
• Monitor, document and/or follow-up on participant adverse events.
• May coordinate Basic and Advanced Life Support courses for Clinical Operations team members.
• Maintain and advocate a high level of customer service, quality, and safety within the department.
• May assist in study related consenting with participant screenings.
• May train employees on clinical trial activities associated to their job needs.
• Provide feedback, where necessary, to appropriate team members of study progress.
• Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
• Can act as a Facilitator for psychedelic studies, when necessary

What You’ll Need to Succeed

• Degree from accredited Registered Nurse program required or bachelor’s degree in nursing from an accredited school.
• Ordre des infirmiers et infirmières du Québec (OIIQ) license required;
• 1-3 years of related work experience.
• Good Communication in French and English, customer service focused, able to work in fast-paced environment.

What We Offer

• On site position at our Montreal site (1200 Beaumont);
• Accessible by public transportation (Metro L’ Acadie), Free parking for employees;
• Regular permanent position ;
• 37.5 hours per week;
• Availability every other weekend is required;
• Day, evening or night shift (no shift rotation).

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

• Perform scheduled inspection of emergency crash carts, inventory/inspect the contents, and maintain up to date records.
• Act as a mentor to Clinical Operations team members.
• Ensure the confidentiality of clinical trial participants and sponsors is respected.
• Continuously assess safety improvement opportunities and communicate with departmental management.
• Perform clinical trial activities including but not limited to, continuous monitoring, safety assessments, Investigational Product (IP) administration and catheter installation.
• Monitor, document and/or follow-up on participant adverse events.
• May coordinate Basic and Advanced Life Support courses for Clinical Operations team members.
• Maintain and advocate a high level of customer service, quality, and safety within the department.
• May assist in study related consenting with participant screenings.
• May train employees on clinical trial activities associated to their job needs.
• Provide feedback, where necessary, to appropriate team members of study progress.
• Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
• Can act as a Facilitator for psychedelic studies, when necessar