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 & 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.
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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.
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
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
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
