Senior PK Analyst (R/SAS) – Remote

Parexel

Atlanta (GA)

Remote

USD 120,000 - 150,000

Full time

9 days ago

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Job summary

Parexel is seeking a Senior PK Analyst to be based remotely, within listed eligible countries, including the United States. The role focuses on deriving PK/PD parameters and programming datasets using SAS and R, with NONMEM experience preferred.

Candidates should be comfortable working independently on complex clinical projects. They will support sponsors and CPMS teams, mentor others, and ensure regulatory compliance with ICH/GCP standards while delivering high-quality results across tables,

Qualifications

  • Bachelor's degree in programming, statistics or mathematics or equivalent.
  • Strong programming skills in SAS and R; experience with NONMEM preferred.
  • Experience with regulatory expectations and Good Clinical Practice is advantageous.

Responsibilities

  • Derivation of Pharmacokinetic (PK) and Pharmacodynamic (PD) parameters.
  • Programming and validation of NONMEM datasets and PK/PD derived datasets.
  • Programming and validation of tables, listings, figures, and statistical appendices when applicable.
  • Execute activities according to SOPs and timelines with high quality.
  • Ensure deliveries meet agreed specifications and expectations.
  • Apply good programming practices; follow ICH and GCP standards.
  • Actively participate in or lead process and quality improvement initiatives.
  • May serve as process/system owner in collaboration with key stakeholder functions.

Skills

Analytical thinking
Attention to detail
Strong communication skills
Project management
English language proficiency

Education

Bachelor's degree in programming, statistics or mathematics

Tools

SAS
R
Phoenix WinNonlin
Unix/Linux

Job description

Parexel is seeking a Senior PK Analyst to be based remotely, within listed eligible countries, including the United States. The role focuses on deriving PK/PD parameters and programming datasets using SAS and R, with NONMEM experience preferred.

Candidates should be comfortable working independently on complex clinical projects. They will support sponsors and CPMS teams, mentor others, and ensure regulatory compliance with ICH/GCP standards while delivering high-quality results across tables,

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