Remote Nonclinical Scientist Consultant II (Contract)

GForce Life Sciences

Princeton (NJ)

On-site

USD 85,000 - 110,000

Full time

47 hours ago
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Job summary

GForce Life Sciences in Princeton, NJ, offers a remote, EST-hours Scientist Consultant (QC/AS) II contract role focused on nonclinical studies and regulatory compliance. You will lead study management, coordinate CROs, and ensure timely QC documentation throughout the project lifecycle.

The role requires 3–5 years in industrial DMPK, with strong communication and organizational skills. BS/MS or PhD backgrounds in related fields are welcomed, with outsourcing experience valued.

Qualifications

  • 3–5 years of industrial DMPK experience in pharma/biotech or CRO settings.
  • Experience supporting nonclinical studies with outsourcing involvement is a plus.
  • Knowledge of preclinical PK, MetID, and drug–drug interactions is highly desirable.

Responsibilities

  • Assist in managing contract laboratories for nonclinical studies and scheduling.
  • Coordinate vendor contracts including MSAs, Quality Agreements, CDAs, and financials.
  • Procure and track reference materials at analytical labs and review results for accuracy.
  • Provide scientific input on study design, data analysis, and interpretation of results.
  • Prepare and maintain QC docs like protocols, reports, and test methods.
  • Audit external CROs and labs to ensure compliance and quality standards.
  • Manage study timelines to meet project objectives and regulatory submission materials.

Skills

DMPK experience
In vitro/in vivo support
Outsourcing experience
Preclinical PK knowledge
Study coordination
Regulatory liaison/communication

Education

Bachelor's or Master's in Chemistry/Biology/Pharmaceutical Sciences/Pharmacokinetics/Toxicology

Job description

GForce Life Sciences in Princeton, NJ, offers a remote, EST-hours Scientist Consultant (QC/AS) II contract role focused on nonclinical studies and regulatory compliance. You will lead study management, coordinate CROs, and ensure timely QC documentation throughout the project lifecycle.

The role requires 3–5 years in industrial DMPK, with strong communication and organizational skills. BS/MS or PhD backgrounds in related fields are welcomed, with outsourcing experience valued.

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