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Posted 2 days ago

PK Scientist I

@ Altasciences Company Inc

Laval, QC · Montréal, QC

RemoteFull-time2+ years experience
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SIGNALS

Overview

Altasciences Company Inc is hiring a PK Scientist I to serve as the pharmacokinetics representative on sponsor project teams, performing PK and toxicokinetic analysis and preparing scientific documents. The role covers protocol and SAP review, non-compartmental analysis in Phoenix WinNonlin, and QC of team deliverables. Full-time, with benefits including health insurance, an RRSP with employer match and paid leave.

Responsibilities:

  • Serve as PK representative on assigned project teams
  • Perform non-compartmental and toxicokinetic analysis
  • Prepare and review PK sections of CSRs and SAPs
  • Perform QC review of team documents
  • Contribute to risk assessment plans

Requirements summary:

  • Bachelor's in pharmacy, pharmacology or related field
  • Minimum 2 years PK experience
  • Experience with Phoenix WinNonlin
  • Excellent English communication skills
  • Understanding of regulatory guidelines and drug development

Tools & skills

Benefits mentioned

DentalVisionRetirement planEmployee assistancePaid time off
Source and dates

Employer career site / ATS feed · workday

Employer posting date
2026-11-04
First seen by our source
2026-11-05
Source record updated
2026-11-05

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

Job details

SeniorityEntry level
DepartmentPhysicians & advanced practice
Experience2+ years
Hours per week40 (estimated)
Work settingOffice
PositionMostly sitting
Physical demandsphysical low · computer high
LanguagesEnglish, French
EducationBachelor’s degree (required)
Fields of studyPharmacy, Pharmacology
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
  • 10103 Metcalf Ave, Overland Park, Kansas 66212, US
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  • 1510 Delp Dr, Harleysville, Pennsylvania 19438, US
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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…

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 PK Scientist I is responsible for gathering and synthesizing scientific information, performing PK analysis, and providing high-quality documents to support sponsors' research programs.

What You'll Do Here

  • Serve as the PK representative or nonclinical principal investigator or contributing scientist on assigned project teams.
  • Review of protocols for studies of moderate complexity.
  • Prepare and/or review data transfer agreements (DTAs).
  • Prepare and/or review protocol deviation impact assessments, sample inventory summaries (SIS), and PK population determinations.
  • Prepare and/or review PK sections of statistical analysis plans (SAPs) for studies of simple to moderate complexity.
  • Perform non-compartmental PK analysis for studies of simple to moderate complexity using Phoenix WinNonlin software.
  • Perform toxicokinetic (TK) analysis and prepare nonclinical reports in accordance with project/client specifications and Good Laboratory Practice (GLP).
  • Provide critical interpretation of PK results.
  • Prepare and/or review of PK sections of clinical study reports (CSRs), preliminary results summaries, and standalone reports for studies of simple to moderate complexity in accordance with project/client specifications and International Conference on Harmonisation (ICH) E3 guidance.
  • Review and provide assistance in answering deficiency letters from regulatory agencies, as required.
  • Perform literature searches/reviews as necessary to obtain background information for analyses and interpretation.
  • Perform quality control (QC) review of analyses and documents prepared by other team members for completeness, accuracy, consistency, and structure.
  • Actively participate in internal and external project team meetings, as required.
  • Coordinate with internal team to deliver high-quality documents in accordance with agreed upon timelines.
  • Contribute to risk assessment and management plans (RAMPs) for assigned studies.
  • Conduct all work in compliance with standard operating procedures (SOPs), Good Clinical Practice (GCP), and all regulatory guidelines.
  • Maintain familiarity with client expectations and produce analyses and documents consistent with these.
  • Have awareness of regulatory guidelines of related authorities (Therapeutic Products Directorate [TPD], Food and Drug Administration [FDA], European Medicines Agency [EMA], etc) as well as ICH and GCP procedures.May participate in departmental or interdepartmental quality improvement initiatives.
  • Maintain and participate in the objectives of the department.

What You'll Need to Succeed

  • Bachelor’s Degree in Pharmacy, Pharmacology, or relevant field (experience may be substituted for education)
  • Minimum of 2 years experience as PK.
  • Experience in a non clinical TK setting an asset.
  • Experience with Phoenix WinNonlin.
  • Excellent verbal and written communication skills.
  • Professional attitude and strong interpersonal skills.
  • Ability to acquire and apply knowledge quickly.
  • Ability to work well with a multi-disciplinary team of professionals.
  • Client-focused approach to work.
  • Flexible attitude with respect to work assignments and new learning.
  • Ability to prioritize workload.
  • Understanding of clinical research, pharmacology and PK, drug development process, and applicable regulatory guidelines.
  • Good computer skills (Microsoft Word, Excel, and Power Point) and ability to understand and adapt to various information technology (IT) systems.

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 PK Scientist I 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.
  • The employee communicates frequently with Altasciences employees across Canada and the United States. As such, English is the main language used to correspond between offices.
  • The employee frequently communicates with English-only customers outside the province of Quebec.

What We Offer

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

#LI-JG1

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