Posted 5 days ago
Clinical Research Technician
@ Altasciences Company Inc
Overview
Altasciences Company Inc is hiring a part-time Clinical Research Technician to carry out clinical trial activities with clinic teams, following protocols, GCP and SOPs. The work includes sample handling, safety measurements, oral IP administration and questionnaires, on site in Montreal. Variable hours on day, evening or night shifts, with full-time daytime availability needed for the first 6 to 8 weeks of training.
Responsibilities:
- Execute clinical trial activities per protocol, GCP and SOPs
- Handle samples, safety measurements and oral IP administration
- Prepare and clean workstations
- Report procedural deviations to supervisors
- Maintain participant confidentiality and customer service
Requirements summary:
- High school diploma or health-related diploma
- Excellent communication in French and English
- Knowledge of another language an asset
- Customer service focus
- Able to work in a fast-paced environment
Tools & skills
Source and dates
Employer career site / ATS feed · workday
- Employer posting date
- 2026-11-02
- First seen by our source
- 2026-10-08
- Source record updated
- 2026-11-06
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Entry level |
| Department | Allied health |
| Schedule | day, evening, overnight |
| Travel | air: none · ground: none |
| Work setting | Hospital or clinic, Laboratory |
| Position | Sitting and standing |
| Physical demands | physical low · computer low |
| Languages | English, French |
| Education | High school (required) |
| Fields of study | health |
| Perks mentioned | Performance bonus, Transit support, Paid training |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Altasciences Company Inc
Saved company profile
Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.
Quicker go/no-go decisions with integrated preclinical, clinical, bioanalytical, manufacturing, and CRO services.
Full company description
Outsourcing made easy with a one-stop solution to early-phase drug development. We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones sooner by improving speed and ease from lead candidate selection to clinical proof of concept, and beyond. When partnering with Altasciences, you can experience up to 40% in time savings thanks to our integrated, one-stop solution offering. We strive to create a true partnership with our clients, our partners, and our colleagues that enables a mutually supporting relationship built on a combination of excellent science and solid communication. Helping sponsors get better drugs to the people who need them, faster, for over 30 years. Our full-service offering is always tailored to your specific research needs: - Preclinical research - Clinical pharmacology - Drug formulation - Manufacturing and analytical services - Bioanalysis - Program management - Medical writing - Biostatics - Data management - And so much more!
- LinkedIn followers
- 43,874
- People associated on LinkedIn
- 1,911
- Reported office locations
- 575 Boulevard Armand-Frappier, Laval, Quebec H7V 4B3, CA
- 1200 Avenue Beaumont, Montreal, Quebec H3P 3P1, CA
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- 130 Discovery Dr, Scott, Pennsylvania 18447, US
- 562 State Road DD, Auxvasse, Missouri 65231, US
- Business categories
- Health Care
- Medical Device
- Wellness
- Biotechnology
- Medical
- Other recorded names
- CareAbout
- Altasciences
- Specialties
- Clinical Research
- Clinical Trials
- Phase I-II
- Human Abuse Liability & Abuse Potential
- Early Cardiac Safety & TQT
- Biosimilars
- Bioanalytical Laboratory
- Analytical Services
- Toxicology Study
- CDMO
- Safety Pharmacology
- Preclinical Study
- GLP / Non-GLP Study
- IND-Enabling
- NDA Submission
- LCMS and LBA
- Small and Large Molecule Bioanalysis
- Research Support Services
- Medical Writing
- Clinical Project Management
- and Pharmaceutical Manufacturing
- Profile identifies a recruitment agency
- No
- Reported total investment
- 0
Currency and observation date were not supplied; this is not a current valuation or a funding round.
Outsourcing made easy with a one-stop solution to early-phase drug development. We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones…
| Field | Value |
|---|---|
| Industry | Research Services |
| Company size | 1,001-5,000 employees |
| Headquarters | Laval, Quebec |
| Organization type | Privately Held |
| Year founded | 1995 |
| Specialties | Clinical ResearchClinical TrialsPhase I-IIHuman Abuse Liability & Abuse PotentialEarly Cardiac Safety & TQTBiosimilarsBioanalytical LaboratoryAnalytical ServicesToxicology StudyCDMO |
| Open jobs on Jobsy | 28 |
| View page |
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
Journal
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