Pharmacokinetics Scientist – Non-Compartmental Analysis (NCA)
Top Benefits
About the role
We are looking for a Pharmacokinetics (PK) Scientist with hands-on experience in non-compartmental analysis (NCA) to join our team. The successful candidate will support both early- and late-phase clinical trials by performing PK analyses, interpreting results, and contributing to regulatory documents. This role offers a hybrid remote arrangement for qualified applicants. The level of responsibility and autonomy will be tailored to the candidate's experience.
About PhinC Modeling
PhinC Modeling is a fast-growing contract research organization dedicated to advancing drug development. We support programs across all phases and therapeutic areas with a focus on scientific rigor, regulatory compliance, and teamwork.
Key Responsibilities
- Perform non-compartmental PK analyses using Phoenix WinNonlin (required), and interpret PK data.
- Contribute to protocol design, especially sections concerning PK objectives, sampling strategy and methods
- Author and review PK analysis plans and reports for internal and regulatory use.
- Conduct QC of PK outputs and maintain high documentation standards.
- Apply knowledge of CDISC standards (SDTM and ADaM) for structuring and reviewing PK datasets and their documentation.
- Prepare and review data specification documents (DTAs), manage dataset transfers, and ensure datasets are complete, consistent, and ready for import into analysis platforms.
- Collaborate with clinical, data management, and bioanalytical teams on study planning and PK data management.
- Manage study timelines and ensure workload follow-up and timely delivery.
- Communicate findings clearly with internal and external stakeholders.
Additional Responsibilities (Based on Experience)
- Provide strategic input on study design and regulatory interactions.
- Lead complex PK projects across development stages.
- Mentor junior scientists and contribute to internal process improvement.
Qualifications
- Degree in Pharmacokinetics, Pharmaceutical Sciences, Pharmacology, Biomedical Engineering, or related field:
- Bachelor’s with 5+ years’ experience
- Master’s with 3+ years’ experience
- PhD with 1–3+ years’ experience
- Solid understanding of PK principles and hands-on experience in NCA.
- Proficiency in Phoenix WinNonlin is required; knowledge of R or SAS is a plus.
- Familiarity with regulatory guidelines (FDA, EMA) for PK analysis is an asset.
- Strong written and oral communication in both English and French.
- Detail-oriented with strong organizational and problem-solving skills.
What We Offer
- Competitive salary based on experience
- Comprehensive benefits package
- Flexible and supportive work environment
- Career development through training and mentorship
Help us move medicines from lab to life!
PhinC Modeling proudly embraces diversity and is an Equal Opportunity Employer.
About PhInc. Modeling
Pharmacokinetics Scientist – Non-Compartmental Analysis (NCA)
Top Benefits
About the role
We are looking for a Pharmacokinetics (PK) Scientist with hands-on experience in non-compartmental analysis (NCA) to join our team. The successful candidate will support both early- and late-phase clinical trials by performing PK analyses, interpreting results, and contributing to regulatory documents. This role offers a hybrid remote arrangement for qualified applicants. The level of responsibility and autonomy will be tailored to the candidate's experience.
About PhinC Modeling
PhinC Modeling is a fast-growing contract research organization dedicated to advancing drug development. We support programs across all phases and therapeutic areas with a focus on scientific rigor, regulatory compliance, and teamwork.
Key Responsibilities
- Perform non-compartmental PK analyses using Phoenix WinNonlin (required), and interpret PK data.
- Contribute to protocol design, especially sections concerning PK objectives, sampling strategy and methods
- Author and review PK analysis plans and reports for internal and regulatory use.
- Conduct QC of PK outputs and maintain high documentation standards.
- Apply knowledge of CDISC standards (SDTM and ADaM) for structuring and reviewing PK datasets and their documentation.
- Prepare and review data specification documents (DTAs), manage dataset transfers, and ensure datasets are complete, consistent, and ready for import into analysis platforms.
- Collaborate with clinical, data management, and bioanalytical teams on study planning and PK data management.
- Manage study timelines and ensure workload follow-up and timely delivery.
- Communicate findings clearly with internal and external stakeholders.
Additional Responsibilities (Based on Experience)
- Provide strategic input on study design and regulatory interactions.
- Lead complex PK projects across development stages.
- Mentor junior scientists and contribute to internal process improvement.
Qualifications
- Degree in Pharmacokinetics, Pharmaceutical Sciences, Pharmacology, Biomedical Engineering, or related field:
- Bachelor’s with 5+ years’ experience
- Master’s with 3+ years’ experience
- PhD with 1–3+ years’ experience
- Solid understanding of PK principles and hands-on experience in NCA.
- Proficiency in Phoenix WinNonlin is required; knowledge of R or SAS is a plus.
- Familiarity with regulatory guidelines (FDA, EMA) for PK analysis is an asset.
- Strong written and oral communication in both English and French.
- Detail-oriented with strong organizational and problem-solving skills.
What We Offer
- Competitive salary based on experience
- Comprehensive benefits package
- Flexible and supportive work environment
- Career development through training and mentorship
Help us move medicines from lab to life!
PhinC Modeling proudly embraces diversity and is an Equal Opportunity Employer.