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Posted 22 days ago

Scientist, Pk & Biomarker

@ Altasciences Company Inc

Laval, Quebec

On-siteFull-time3+ years experience
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SIGNALS

Overview

Altasciences Company Inc is hiring a Scientist, PK & Biomarkers to develop, run, report and troubleshoot bioanalytical assays for regulated clinical and preclinical studies. The role acts as Bioanalytical Principal Investigator and client contact on assigned projects, and mentors analysts. Full-time, with a benefits package and telework when applicable.

Responsibilities:

  • Develop, run and troubleshoot multiple assay types
  • Serve as Bioanalytical Principal Investigator and client contact
  • Review data batches and trends, and manage deviations
  • Write and update method SOPs
  • Mentor analysts and support team members

Requirements summary:

  • College or university degree in chemistry, biochemistry or immunology
  • About 3 years of regulated clinical or preclinical experience preferred
  • Knowledge of GLP and regulatory guidelines
  • Excellent troubleshooting and attention to detail
  • Written and verbal communication in French and English

Tools & skills

Benefits mentioned

DentalVisionRetirement planEmployee assistancePaid time off
Source and dates

Employer career site / ATS feed · workday

Employer posting date
2026-10-15
First seen by our source
2026-10-16
Source record updated
2026-11-04

These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.

Job details

SeniorityMid level
DepartmentPhysicians & advanced practice
Experience3+ years
Hours per week40 (estimated)
Travelair: none · ground: none
Work settingLaboratory
PositionSitting and standing
Physical demandsphysical low · computer moderate
LanguagesEnglish, French
EducationBachelor’s degree (preferred)
Fields of studyChemistry, Biochemistry, Immunology
Perks mentionedGenerous 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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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…

FieldValue
IndustryResearch Services
Company size1,001-5,000 employees
HeadquartersLaval, Quebec
Organization typePrivately Held
Year founded1995
SpecialtiesClinical ResearchClinical TrialsPhase I-IIHuman Abuse Liability & Abuse PotentialEarly Cardiac Safety & TQTBiosimilarsBioanalytical LaboratoryAnalytical ServicesToxicology StudyCDMO
Open jobs on Jobsy28
LinkedInView page
Job description

About The Role
The Scientist, PK & Biomarkers is assigned to projects based on scientific competency and training. The Scientist will ensure the overall integrity/quality of assigned studies.

The Scientist can also be designated as the main contact for client interactions laboratory for their assigned projects.

What You'll Do Here

  • Autonomous and proficient developing, planning, managing, conducting, reporting and troubleshooting multiple assay types to ensure scientific quality, regulatory expectations, and client satisfaction.

  • Assigned by management on studies and tasks based on scientific competency and training (can include method development, validation or sample analysis projects).

  • For validations and sample analysis the Scientist can be assigned as Bioanalytical Principal Investigator and is the first point of contact for PM and/or clients for laboratory services and will manage and conduct method development, qualification , validation and production studies for clinical and non-clinical studies in compliance with the protocol/study plan, amendments, GCP, GLPs, SOPs and Best Practices.

  • Manage project and order appropriate material, as needed.

  • When applicable, provide QC support on studies assigned to other team members in laboratory based on training and competencies.

  • When applicable, perform data batch review, perform multi-batch trend analysis, complete documentation as required by tracking deviations, events and reports of non-compliance and review or approved Memo to File or SOP/Protocol/Study Plan deviations.

  • When applicable, provide a report and/or reporting of results, within study timelines and ensure any deviations/exception events are reflected as appropriate and assure that all analysis conducted is reported and is accurate.

  • Manage as to maintain timeline and scheduling commitments.

  • When applicable review and provide comments and recommendations, as needed, for the bioanalytical portions of preclinical and clinical protocols, study plans, laboratory manuals, Data Transfer Agreements, and/or other document, as needed.

  • Support and mentor Analysts in the daily operations for completion of sample analysis and/or validation studies and the analysts work.

  • Support and mentor other team members based on expertise.

  • Responsible for troubleshooting issues within the studies and be able to resolve them independently via development of appropriate procedure.

  • Organize and communicate complex data sets in a clear and concise manner to key stakeholders from diverse backgrounds.

  • Write, review and updated method SOP as needed.

  • Participate in meetings with clients, conferences and scientific outreach.

  • Conduct applicable work in compliance with applicable SOPs, GCPs, GLPs, and observe all company guidelines and policies.

  • Respecting Health and Safety standards in terms of personal protection, laboratory maintenance, and work procedures.

What You'll Need to Succeed

  • Ideally College degree and/or University degree in Chemistry, Biochemistry, Immunology or applicable field.

  • Preferred experience in regulated clinical and/or preclinical studies with typically 3 years of experience.

  • Knowledge of regulatory agency guidelines, must understand general SOPs and have excellent knowledge of GLP regulations.

  • Good organizational skill.

  • Highly flexible.

  • Sense of urgency.

  • Excellent troubleshooting skills.

  • Client oriented.

  • Attentive to details.

  • Ability to coach/mentor people.

  • Good communication both written and verbal in French & English.

Altasciences strives to provide a French work environment for its employees in Quebec. Altasciences has taken all reasonable measures to avoid imposing the above language requirement. This requirement is essential for the position of Scientist, PK & Biomarkers in particular, but without limitation, for the following reason(s):

  • The requirement to have study protocols read and documented in English as required by industry regulatory agencies

What We Offer

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences’ Benefits Package Includes:

  • Health/Dental/Vision Insurance Plans

  • 401(k)/RRSP with Employer Match

  • Paid Vacation and Holidays

  • Paid Sick and Bereavement Leave

  • Employee Assistance & Telehealth Programs

  • Telework when applicable

Altasciences’ Incentive Programs Include:

  • Training & Development Programs

  • Employee Referral Bonus Program

  • Annual Performance Reviews

#LI-MB1

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