At a Glance
- Tasks: Develop and quality control NONMEM PK/PD datasets for drug development.
- Company: Join ICON plc, a leader in healthcare intelligence and clinical research.
- Benefits: Competitive salary, health insurance, flexible benefits, and global support programmes.
- Other info: Be part of a diverse culture that values talent and innovation.
- Why this job: Make a real impact on innovative drug development in a collaborative environment.
- Qualifications: Bachelor's degree and 6 years' experience in pharma or biotech with strong R programming skills.
The predicted salary is between 63000 - 77000 £ per year.
ICON plc is a world-leading healthcare intelligence and clinical research organization.
We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
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.
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.
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.
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Pharmacometrics Support Programmer in Reading 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.
StudySmarter Expert Advice🤫
We think this is how you could land Pharmacometrics Support Programmer in Reading
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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 Strategic Solutions!
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 Strategic Solutions that you're not just a fit for the job but also a safety-conscious candidate!
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How to prepare for a job interview at ICON Strategic Solutions
✨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 Strategic Solutions 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.
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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.
