Clinical Research Technician

Altasciences Company; Montreal; Presencial; CAD 40 000 - 55 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

On-site Montreal location

Public transportation access

Free employee parking

Training & Development Programs

Employee Referral Bonus Program

Resumo da oferta

Altasciences is seeking a Clinical Research Technician to collaborate with clinic teams and execute trial activities in a GCP/SOP-compliant manner. The role requires handling samples, safety measures, and protocol-driven events while maintaining participant confidentiality and high service standards.

The position is on-site at our Montreal location and involves variable hours with day, evening or night shifts across a full-time schedule. Fluency in English and French is essential.

Qualificações

• High School Diploma or health-related diploma.
• Excellent communication skills in French and English.
• Knowledge of another language is an asset.
• Customer service oriented.
• Able to work in a fast-paced environment.

Responsabilidades

• Execute clinical trial activities in compliance with study protocol, GCP and SOPs.
• Maintain confidentiality of participants and sponsors.
• Understand protocol-driven study events and collection windows.
• Report deviations to supervisory teams.
• Prepare and clean work stations (urine collection, blood processing, etc.).
• Handle samples, safety measurements, oral IP administration, and questionnaires as applicable.
• Provide high-level customer service and coordinate with study teams.
• Communicate issues and resolutions to supervisors.
• Complete required training and other tasks as assigned.

Conhecimentos

French & English

Customer service

Fast-paced environment

Formação académica

High School Diploma

Descrição da oferta de emprego

About the role

The Clinical Research Technician will work with Clinic teams to execute clinical trial activities. Responsibilities of the Clinical Research Technician include execution of tasks performed/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s. Please note that this is a variable status position.

What you'll do here

• Ensure the confidentiality of clinical trial participants and sponsors is respected;
• Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events;
• Report procedural deviations to appropriate supervisory team members;
• Preparation and proper clean-up of applicable work-stations (i.e. urine collection station, blood processing station, etc.);
• Maintain and advocate a high level of customer service, quality and safety within the department;
• Perform clinical trial activities may include but not limited to, sample handling, safety measurements, oral IP administration, and questionnaire administration;
• Conduct all clinical trial activities and participant interaction with a high standard of customer service;
• Report significant participant misbehavior to Study/Clinical Operations management teams;
• Provide feedback, where necessary, to appropriate team members of study progress;
• Proactively communicate issues and/or problem resolutions to departmental supervisors and managers;
• Complete and/or maintain training as required per jobs needs;
• Other tasks as assigned by management.

What you'll need to succeed

• High School Diploma or/and Diploma related to the field of health;
• Excellent communication skills in French and English;
• Knowledge of another language an asset;
• Customer service focused;
• Able to work in fast-paced environment.

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 Technician 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

• You must be available full-time during the day for the first 6 to 8 weeks of training.
• Variable hours.
• Day, evening or night shift (no shift rotation).
• On site position at our Montreal site (1200 Beaumont);
• Accessible by Public Transportation (Metro L'Acadie), Free Parking for employees.

Altasciences' Incentive Programs Include:

• Training & Development Programs
• Employee Referral Bonus Program