Clinical Research Nurse

CareAbout•Montreal, QC

1d•Onsite

About The Position

At Altasciences, we are dedicated to assisting in the discovery, development, and manufacturing of new drug therapies to expedite their delivery to patients in need. Every role contributes significantly to improving global health and well-being. We foster a passionate and collaborative work environment by living our values of Employee Development, Customer Focus, Quality and Excellence, Respect, and Integrity. We are seeking talented and enthusiastic individuals to join our growing team, whether you are a recent graduate or looking for your next career move. We believe we are better together and embody the spirit of 'We Are Altasciences.' The Clinical Research Nurse will be responsible for overseeing the safety and consent of clinical trial participants during study conduct and ensuring the maintenance of safety equipment. This role involves executing tasks in strict compliance with study protocols, Good Clinical Practices (GCP), and Standard Operating Procedures (SOPs).

Requirements

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.
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.

Nice To Haves

Relevant industry experience a plus.

Responsibilities

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.