Pharmacometrics Support (base) At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. We are seeking an experienced Pharmacometrics Support Programmer to join a global FSP team. This is an opportunity for a highly analytical programmer with strong R programming expertise and experience in PK/PD data preparation to contribute to critical drug development programmes. In this role, you will be responsible for the creation, quality control, and standardisation of NONMEM PK/PD datasets, supporting pharmacometric modelling activities across a diverse clinical portfolio. Working closely with Data Management, Statistical Programming, Statistics, Bioanalytical teams, and external partners, you will play a key role in ensuring high-quality pharmacometric data is delivered on time and to the highest regulatory standards. Key Responsibilities Develop and quality control NONMEM PK/PD datasets using SDTM and ADaM data sources. Support pharmacometric modelling activities by delivering accurate, complete, and submission-ready datasets. Perform quality review of internally and externally produced NONMEM datasets. Collaborate with Data Management, Statistical Programming, Statistics, Clinical Pharmacology, and Bioanalytical teams to resolve data issues and ensure project timelines are met. Contribute to the preparation of regulatory submission projects in accordance with internal pharmacometrics guidelines. Conduct quality control testing of customised R packages used to standardise pharmacometric workflows. Develop and maintain testing frameworks and validation processes for departmental R tools and packages. Identify data discrepancies, process improvements, and opportunities for greater automation and efficiency. Actively contribute to the development and implementation of new pharmacometric standardisation initiatives. Ensure all deliverables comply with applicable SOPs, working instructions, regulatory requirements, and ICH-GCP guidelines. Maintain inspection readiness through ongoing training and adherence to quality standards. What We're Looking For Bachelor's degree in a Life Science, Health Science, Statistics, Computer Science, IT, or related discipline. Minimum of 6 years' experience within the pharmaceutical, biotechnology, or CRO industry. Strong programming expertise in R. Experience developing and quality controlling NONMEM PK/PD datasets. Working knowledge of PK/PD principles and pharmacometric workflows. Strong understanding of SDTM, ADaM, and CDISC standards, including controlled terminology. Experience supporting NONMEM file creation, quality control, submissions, and standardisation activities. Strong attention to detail and commitment to data quality. Excellent written and verbal communication skills in English. Desired Skills Experience reviewing and managing outsourced programming deliverables. Experience validating or quality controlling customised R packages. Demonstrated ability to identify process improvements and drive standardisation initiatives. Ability to work effectively across global, cross-functional teams. Why Join Us? Opportunity to work within a globally recognised Clinical Pharmacology
Statistical Programmer II (PK) employer: ICON Strategic Solutions
ICON plc is an exceptional employer located in Reading, offering a dynamic work culture that prioritises quality and compliance in clinical trials. Employees benefit from competitive salaries, comprehensive benefits, and ample opportunities for professional growth through collaboration with cross-functional teams and participation in audits. The company's commitment to excellence and innovation makes it a rewarding place for those looking to make a meaningful impact in the field of clinical research.
