Job Region: New Jersey

  • Develop and review protocols, analysis plans, and study reports
  • Conduct PK analysis
  • Prepare CIB/IMPD/IND and other regulatory documents
  • Represent PKDM and formulate strategies for specific projects

Additional duties:

  • Perform complex non-compartmental PK analysis
  • Perform compartmental PK analysis and simulation
  • Perform PK/PD analysis

PhD with 3+ years experience required.

With guidance, perform non-compartmental pharmacokinetic (PK) data analysis and reporting for regulatory submission using WinNonlin. Under direction, provide inputs to designing clinical pharmacology studies, protocol development, and provide support to study execution. Assist in the planning, implementing, interpreting and reporting of assigned Phase I to III studies. Under direction, devise PK and PK-PD analysis planContinue Reading


400 Crown Colony Drive, Suite 600

 Quincy, MA 02169

T: 617-689-0029 • F: 617-689-3044

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