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88,000+ live jobsPermanent contract
Per the ad.
Fully remote
Per the ad.
Have the right to work in Spain
ICON plc doesn't mention sponsorship in the ad.
Work in English
English is required, per the ad.
Have 6+ years of experience
Mid-level role.
University degree
“Bachelor's degree in a Life Science, Health Science, Statistics, Computer Science, IT, or related discipline.” — per the ad.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
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.
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.
Pharmacometrics Support Programmer
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.
About the Role
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.
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.
Opportunity to work within a globally recognised Clinical Pharmacology & Pharmacometrics function.
Contribute directly to innovative drug development programmes.
Work in a highly collaborative and scientifically driven environment.
Be part of ongoing innovation and standardisation initiatives within pharmacometrics and clinical data science.
Use your expertise to influence best practices and improve the efficiency and quality of pharmacometric deliverables.
If you are passionate about leveraging R programming, pharmacometrics, and data quality excellence to support drug development, we'd love to hear from you.
What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
Visit our careers site to
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
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