Posted 2 months ago
Licensed Practical Nurse - Clinical Operations
@ Altasciences Company Inc
Montréal, Quebec
Overview
Altasciences Company Inc is hiring a part-time Licensed Practical Nurse for its clinical operations team in Montreal. The role oversees participant safety during clinical trials, performs safety assessments, blood collection, medication administration, ECGs and vital signs, and monitors adverse events. Work is on site with day, evening or night shifts, one weekend in two, and full-time availability during the first 6 to 8 weeks of training.
Responsibilities:
- Assess safety of clinical trial participants and maintain safety equipment
- Perform blood collection, ECGs, vital signs and medication administration
- Monitor, document and follow up on adverse events
- Train and mentor Clinical Operations team members
Requirements summary:
- Vocational training in health assistance and nursing
- OIIAQ permit required
- Bilingual French and English proficiency
- Strong written and verbal communication skills
Tools & skills
Source and dates
Employer career site / ATS feed · workday
- Employer posting date
- 2026-08-30
- First seen by our source
- 2026-10-08
- Source record updated
- 2026-10-14
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Department | Nursing & personal care |
| Schedule | day, evening, weekends, overnight |
| Travel | air: none · ground: none |
| Work setting | Laboratory |
| Position | Sitting and standing |
| Physical demands | physical moderate · computer moderate |
| Languages | English, French |
| Licences & certifications | OIIAQ permit |
| Education | Trade certificate (required) |
| Fields of study | Health assistance, Nursing |
| 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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- 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 Licensed Practical Nurse will assist in overseeing the safety of clinical trial participants during study conduct and the maintenance of safety equipment. The Licensed Practical Nurse will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). Please note that this is a variable status position.
What You'll Do Here
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.
What You'll Need to Succeed
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.
Relevant industry experience a plus.
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 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.
What we offer
On site position at our Montreal site (1200 Beaumont).
Accessible by Public Transportation (Metro L'Acadie), Free Parking for employees.
Day, evening or night shift (no shift rotation).
Must be available to work one weekend out of every two
You must be available full-time during the day for the first 6 to 8 weeks of training.
Altasciences’ Incentive Programs Include:
Training & Development Programs.
Employee Referral Bonus Program.
Annual Performance Reviews.
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