Posted 4 days ago
Clinical Quality Control Associate II
@ Altasciences Company Inc
Overview
Altasciences Company Inc is hiring a full-time Clinical Quality Control Associate II in Montreal. The role reviews clinical trial data for quality, tracks errors and data queries, and works with the Quality Systems team under GCP and SOP requirements. The posting states a 37.5-hour week, availability between 7am and 7pm with one weekend in three, and on-site work at the Beaumont site.
Responsibilities:
- Review clinical trial data for quality control
- Track errors, trends and data queries
- Maintain deviation tracking systems and computer files
- Escalate issues to departmental supervisors
- Coach and mentor Quality Systems team members
Requirements summary:
- High school diploma
- Fluent French and English
- Microsoft Office proficiency
- Detail-oriented and organized
- Discretion with confidential information
- Able to lift up to 25 pounds
Tools & skills
Source and dates
Employer career site / ATS feed · workday
- Employer posting date
- 2026-11-02
- First seen by our source
- 2026-11-03
- Source record updated
- 2026-11-03
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Mid level |
| Department | Allied health |
| Hours per week | 37.5 |
| Schedule | day, evening, weekends |
| Travel | air: none · ground: none |
| Work setting | Office |
| Position | Mostly sitting |
| Physical demands | physical low · lift 25 lb · computer high |
| Languages | English, French |
| Education | High school (required) |
| Perks mentioned | Generous paid time off, Retirement plan, Performance bonus, Wellness, 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 Quality Control Associate is responsible for the quality control (QC) review of clinical trial data and working with the Quality Systems team to complete QC related tasks. The Clinical Quality Control Associate will conduct tasks performed within compliance of study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).
What You’ll Do Here
- Report, track and escalate (if necessary) errors and/or trends that may require re-training, as required by location.
- Compile data and maintain computerized files and/or update deviation tracking systems.
- Record, track and ensure the resolution of data queries.
- Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
- Ensure the confidentiality of clinical trial participants and sponsors is respected.
- Maintain and advocate a high level of quality and customer service within the department.
- May document and/or report clinical trial related deviations (i.e. SOP, protocol).
- Act as a mentor and coach the Quality Systems team members.
- Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events.
- Other tasks as assigned by management
What You’ll Need to Succeed
- High School Diploma completed.
- Related work experience an asset.
- Good Communication in French and English.
- Detail oriented, well organized, customer service focused, able to work in fast-paced environment.
- Software: Microsoft Office.
- Strong attention to details
- Personal/professional integrity and proven discretion in handling confidential information.
- Ability to develop strong trusting relationships in order to gain support and achieve results.
- Capable of managing multiple conflicting priorities.
- Must be self-directed, motivated and have a willingness to take initiative.
- The candidate must be able to lift up to 25 pounds.
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 Quality Control Associate 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
- Regular full-time position; 37.5 hours a week.
- Candidate needs to be available between 7am and 7pm and 1 every 3 week-ends.
- On site, Montreal site (1200 Beaumont).
- Accessible by metro (L'Acadie); Free parking for employees.
Altasciences offers a wide range of benefits to help employees live healthy and satisfying lives, both on and off the job.
Altasciences benefits include
- Health/dental/vision insurance plans
- RRSP with employer match
- Paid vacation and statutory vacations
- Paid sick leave and bereavement leave
- Employee assistance and telehealth programs
Altasciences' incentive programs include
- Training and development programs
- Employee orientation bonus program
- Annual performance reviews
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