At a Glance
- Tasks: Create and quality control NONMEM PK/PD datasets for drug development.
- Company: Join ICON, a global leader in healthcare intelligence and clinical research.
- Benefits: Competitive salary, health coverage, retirement plans, and career development opportunities.
- Other info: Be part of a values-driven organisation focused on integrity, collaboration, and innovation.
- Why this job: Make a real impact on innovative drug programmes while collaborating with global teams.
- Qualifications: Bachelor's degree and 6 years' experience in pharma or biotech; strong R programming skills.
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
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 & 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.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:
- Competitive base salary and performance related incentives.
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance programmes and wellbeing resources.
- Learning and development opportunities through structured training and career pathways.
Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Pharmacometrics Support Programmer employer: IRE
ICON is an exceptional employer that prioritises integrity, collaboration, and inclusion, making it a fantastic place for professionals in the healthcare intelligence and clinical research field. As a Pharmacometrics Support Programmer, you will benefit from a competitive salary, comprehensive health and wellbeing programmes, and ample opportunities for career development within a globally recognised team dedicated to innovative drug development. Join us to contribute to meaningful projects while enjoying a supportive work culture that values your expertise and fosters professional growth.
StudySmarter Expert Advice🤫
We think this is how you could land Pharmacometrics Support Programmer
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like IRE. 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 IRE.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like IRE. 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 IRE is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Pharmacometrics Support Programmer
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 IRE!
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 IRE 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 IRE!
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 IRE, 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 IRE
✨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 IRE 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 IRE’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.
