Associate Director, Clinical Pharmacology Data Programming Specialist

Scorpion Therapeutics; Princeton (NJ); Hybrid; USD 150,000 - 190,000; Full time

Job summary

Scorpion Therapeutics seeks an Associate Director, Clinical Pharmacology Data Programming Specialist to lead data programming and QC activities supporting clinical pharmacology and pharmacometric analyses within the development portfolio.

You will program analysis datasets for PK/PD, exposure-response, and modeling, develop validation strategies, automate workflows, and support regulatory submissions while collaborating with pharmacologists, statisticians, data management, and external vendors.

Qualifications

• Master's degree in Statistics, Biostatistics, Computer Science, or related field.
• Extensive programming experience in R and/or SAS with clinical trial data.
• Knowledge of SDTM, ADaM, CDISC standards.
• Experience supporting pharmacometric analyses (PK/PD).
• Familiarity with NONMEM and related tools preferred.
• 5+ years in biotech/pharma.

Responsibilities

• Program analysis datasets and outputs for PK, PK/PD, exposure–response, NCA, modeling, and biomarkers; develop validation strategies and automate workflows.
• Support regulatory submissions and collaborate cross-functionally with pharmacologists, statisticians, data management, and external vendors.
• Contribute to standards and automation initiatives.

Skills

R

SAS

PK/PD modeling

Clinical trial data

Data programming

Education

Master's degree in Statistics/Biostatistics/Computer Science or related field

Tools

NONMEM

Job description

Role

Associate Director, Clinical Pharmacology Data Programming Specialist, leading data programming and QC activities supporting clinical pharmacology and pharmacometric analyses within Genmab's development portfolio.

Responsibilities

program analysis datasets and outputs for PK, PK/PD, exposure-response, NCA, modeling, and biomarkers; develop validation strategies, automate workflows, and support regulatory submissions; collaborate cross-functionally with pharmacologists, statisticians, data management, and external vendors; contribute to standards and automation initiatives.

Requirements

Master's in Statistics, Biostatistics, Computer Science, or related field; extensive programming experience in R and/or SAS with clinical trial data; knowledge of SDTM, ADaM, CDISC standards; experience supporting pharmacometric analyses (PK/PD, population PK); familiarity with NONMEM and related tools preferred; 5+ years in biotech/pharma.

HighValue

clinical pharmacology, pharmacometrics, PK/PD modeling, regulatory submission support, analysis dataset QC, automation, validation, cross-functional collaboration.

WorkSetup

flexible remote work (20%-40%); some team interactions required.