PK Scientist II

Everest Clinical Research

. Conduct PK/PD data analysis using non-compartmental analysis .

Posted 10/9/2026full-timeRemote • CanadaJuniorMid-Level💰 CA$105,000 - CA$120,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Expertise in PK/PD data analysis and modeling, with proficiency in tools such as Phoenix WinNonlin and R. Strong background in clinical trial design, regulatory submissions, and scientific writing.

Highest-signal resume keywords

PK/PD Data AnalysisPhoenix WinNonlinClinical Trial DesignScientific WritingPharmacokinetics

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Non-Compartmental AnalysisPK/PD ModelingStatistical AnalysisData InterpretationPharmacodynamicsPharmacokineticsRegulatory SubmissionsClinical PharmacologyTherapeutic Area KnowledgeProject Management

Soft Skills

Effective CommunicationLogical ThinkingCreativityInterpersonal SkillsTeamwork

Tools & Technologies

MonolixNLMERSASWinNonlin

Industry Keywords

Clinical TrialsPharmaceuticalsIND/NDA/ANDA SubmissionsSOPsICH Guidelines

About the role

Key responsibilities & impact

Conduct PK/PD data analysis using non-compartmental analysis
Support PK/PD modeling and simulations using Phoenix WinNonlin, NLME, Monolix, R, and related software
Apply strategic direction and vision on PK/PD data analysis to support clinical trial designs, compound development plans, and regulatory submissions
Generate predictive simulations and provide input into trial protocol development
Provide input into clinical trial Statistical Analysis Plans and mock tables, listings, and graphs shells, including PK/PD analysis components
Author standalone PK/PD Analysis Plans, including PK/PD mock shells
Author and/or review PK/PD-related documents and reports, including protocols and PK Study Reports
Contribute to clinical pharmacology sections of protocols, clinical study reports, Investigator's Brochures, briefing documents, and IND/NDA/ANDA submissions
Work with regulatory affairs personnel to provide PK/PD data for regulatory communications and presentations as needed
Maintain and adhere to divisional SOPs, guidelines, therapeutic-area standards, and conventions
Keep current with pharmaceutical drug trial regulator and ICH requirements or guidelines
Plan and carry out professional development

Requirements

What you’ll need

Advanced degree, Ph.D., or M.Sc. in Clinical Pharmacology (including Pharmacokinetics, Pharmacodynamics), Pharmacy, Biopharmaceutics, or related field
At least 2 to 4 years’ experience as a PK Scientist or related role in the pharmaceutical clinical trial environment
Experience in multiple therapeutic areas and Phase I through IV clinical trials is preferred
Proficient in using WinNonlin, or equivalent
Other relevant pharmacometric software for non-compartmental analysis, PK/PD analysis, and modeling is preferred
Familiarity with SAS and/or R is preferred (or willingness to learn and master SAS skills)
Excellent understanding of clinical trials and common clinical trial statistical analysis methods is preferred
Skilled in scientific writing and data interpretation is preferred
Demonstrated ability to understand PK results
Able to communicate effectively, orally and in writing
Demonstrated ability for logical thinking, vision, and creativity necessary to function effectively with a large degree of independence and little supervision
Experience with client relationship management is preferred
Ability to multi-task and manage multiple projects with competing and aggressive timelines
Excellent interpersonal and teamwork skills; detail-oriented, customer-, and quality-focused
Well organized and able to work independently
Strong understanding of fundamental PK/PD and statistical principles

Benefits

Comp & perks

Medical, dental, and vision coverage
Life and AD&D insurance
Short- and long-term disability
Tuition reimbursement
Fitness reimbursement
Employee assistance program (EAP)
Pension plan
Generous paid time off and sick leave
Opportunity to earn a performance based bonus