At a Glance
- Tasks: Create and quality control NONMEM PK/PD datasets for drug development.
- Company: Join ICON, the world's largest FSP organisation with a collaborative culture.
- Benefits: Competitive salary, health insurance, flexible benefits, and global support programmes.
- Other info: Be part of a diverse team driving innovation in pharmacometrics and clinical data science.
- Why this job: Make a real impact in innovative drug development while using your R programming skills.
- Qualifications: Bachelor's degree and 6 years' experience in pharma or biotech, with strong R expertise.
The predicted salary is between 63000 - 77000 £ per year.
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.
Key Responsibilities
- Develop and quality control NONMEM PK/PD datasets using SDTM and ADa M 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, ADa M, 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, Life Works, 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
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Pharmacometrics Support Programmer in Reading employer: ICON
At ICON plc, we pride ourselves on being an exceptional employer that values innovation and collaboration in the healthcare intelligence and clinical research sector. Our supportive work culture fosters professional growth through continuous learning opportunities and a commitment to diversity, ensuring that every employee can thrive while making a meaningful impact in the industry. Located in a dynamic environment, we offer unique advantages such as access to cutting-edge resources and a network of talented professionals dedicated to excellence.
StudySmarter Expert Advice🤫
We think this is how you could land Pharmacometrics Support Programmer in Reading
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like ICON. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like ICON.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like ICON. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what ICON is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Pharmacometrics Support Programmer in Reading
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at ICON!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show ICON that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at ICON!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At ICON, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at ICON
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at ICON that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with ICON’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
