Pharmacometrics Data Programmer - R & NONMEM Expert

ICON Strategic Solutions; Reading; On-site; GBP 65,000 - 90,000; Full time

Benefits offered by this job

Competitive salary

Health insurance offerings

Global benefits programme

Job summary

ICON plc is a world-leading healthcare intelligence and clinical research organisation seeking an experienced Pharmacometrics Support Programmer. The role focuses on R programming and PK/PD data preparation to support critical drug development programmes.

You will create, QC and standardise NONMEM PK/PD datasets, collaborate across Data Management, Statistics and Bioanalytical teams, and contribute to regulatory submissions with a focus on quality and timeliness.

Qualifications

• Bachelor's degree in life science, health science, statistics, computer science, IT or related field.
• Minimum of 6 years' experience in pharma, biotech or CRO.
• Strong programming in R and experience with NONMEM PK/PD datasets.
• Working knowledge of PK/PD principles and CDISC standards.
• Experience supporting NONMEM file creation, quality control and submissions.

Responsibilities

• Create, QC and standardise NONMEM PK/PD datasets using SDTM and ADaM sources.
• Support modelling activities by delivering accurate, submission-ready data.
• Quality review of internal and external NONMEM datasets.
• Collaborate with Data Management, Statistics and Bioanalytical teams to meet timelines.
• Prepare regulatory submission datasets per pharmacometrics guidelines.
• Test and maintain R packages and validation processes.

Skills

R programming

PK/PD data preparation

NONMEM datasets

CDISC standards

Data quality assurance

Regulatory submissions support

Collaboration across teams

Education

Bachelor's degree in Life Science or related field

Tools

R

NONMEM

SDTM/ADaM

Job description

ICON plc is a world-leading healthcare intelligence and clinical research organisation seeking an experienced Pharmacometrics Support Programmer. The role focuses on R programming and PK/PD data preparation to support critical drug development programmes.

You will create, QC and standardise NONMEM PK/PD datasets, collaborate across Data Management, Statistics and Bioanalytical teams, and contribute to regulatory submissions with a focus on quality and timeliness.