Licensed Practical Nurse - Clinical Operations

CareAbout•Montreal, QC

4d•Onsite

About The Position

At Altasciences, we are united in our mission to assist in the discovery, development, and manufacturing of new drug therapies to expedite their delivery to patients. 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 together, We Are Altasciences. About The Role The Licensed Practical Nurse will be responsible for overseeing the safety of clinical trial participants during study conduct and maintaining safety equipment. This role involves executing tasks in compliance with study protocols, Good Clinical Practices (GCP), and Standard Operating Procedures (SOPs). Please note that this is a variable status position.

Requirements

Vocational Training Health, Assistance & Nursing required.
Ordre des infirmières et infirmiers auxiliaires du Québec (OIIAQ) permit is required
Ability to read and interpret technical documents and industry specific manuals.
Ability to write reports and correspondence.
Bilingual proficiency in French/English required
Excellent verbal and written communication skills.
Well-developed interpersonal skills are required.
Personal/professional integrity and proven discretion in handling confidential information.
Ability to develop strong trusting relationships to gain support and achieve results.
Capable of managing multiple conflicting priorities.
Must be self-directed, motivated, and have a willingness to take the initiative to identify and anticipate client needs and make recommendations for implementation.
Fluency in English is an essential requirement for the position of Licensed Practical Nurse, clinical operations 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.
Customer service focused, able to work in fast-paced environment.

Responsibilities

Training/mentoring of Clinical Operations team members.
Ensure the confidentiality of clinical trial participants and sponsors is respected.
Continuously assess safety improvement opportunities and proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
Perform clinical trial activities including but not limited to safety assessments and blood collection.
Administer medication, perform ECG, and assess vital signs.
Monitor, document and/or follow-up on participant adverse events.
Maintain and advocate a high level of customer service, quality, and safety within the department.
Other tasks assigned by management.