Clinical Research Technician

Altasciences

. Work with Clinic teams to execute clinical trial activities .

Posted 11/3/2026part-timeMontreal • CanadaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in executing clinical trial activities in compliance with study protocols, Good Clinical Practices (GCP), and Standard Operating Procedures (SOPs). Strong communication skills in both French and English, with a focus on customer service and participant interaction.

Highest-signal resume keywords

Clinical Trial Activities ExecutionGood Clinical Practices (GCP)Standard Operating Procedures (SOPs)Bilingual Communication (French and English)Customer Service Focus

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Research ActivitiesSample HandlingOral IP AdministrationQuestionnaire AdministrationSafety Measurements

Soft Skills

Excellent Communication SkillsCustomer Service OrientationProblem ResolutionAdaptability in Fast-Paced Environment

Certifications & Qualifications

High School DiplomaDiploma Related to Health Field

Industry Keywords

Confidentiality of Clinical Trial ParticipantsProtocol-Driven Timed Study EventsParticipant InteractionTraining ComplianceVariable Hours

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Work with Clinic teams to execute clinical trial activities
Execute tasks and clinical activities in compliance with study protocol, GCP and SOPs
Ensure confidentiality of clinical trial participants and sponsors
Understand protocol-driven timed study events and acceptable collection windows
Report procedural deviations to supervisory team members
Prepare and properly clean applicable workstations
Maintain and advocate customer service, quality and safety standards
Perform sample handling, safety measurements, oral IP administration, and questionnaire administration
Conduct participant interactions with a high standard of customer service
Report significant participant misbehavior to Study/Clinical Operations management
Provide feedback on study progress
Communicate issues and problem resolutions to supervisors and managers
Complete and maintain required training
Perform other tasks assigned by management

Requirements

What you’ll need

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
Must be available full-time during the day for the first 6 to 8 weeks of training
Fluency in English is an essential requirement
Ability to work day, evening or night shifts with no shift rotation
Variable hours
Clinical research activities performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs)

Benefits

Comp & perks

Accessible by Public Transportation (Metro L'Acadie)
Free Parking for employees
Training & Development Programs
Employee Referral Bonus Program