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- Tasks: Lead and programme statistical studies while ensuring data quality and compliance.
- Company: Join Phastar, an award-winning CRO transforming data into actionable insights.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in drug development and improve patient outcomes.
- Qualifications: BSc in a relevant field and SAS programming experience in the pharmaceutical industry.
- Other info: Be part of a diverse team that values excellence, collaboration, and innovation.
The predicted salary is between 36000 - 60000 £ per year.
As an experienced programmer, you will hold a combined project leadership and hands‑on technical statistics role. Working across a defined area within the sponsor team you will be leading studies and working on sponsor systems.
Responsibilities
- Program and validate datasets and SDTMs, including complex efficacy, labs, etc.
- Adhere to client SOPs and work on client systems.
- Oversight of Vendor Programming.
- Knowledge of FDA CRT requirements including define.xml and define.pdf.
- Lead team and be responsible for creation of CRT packages.
- Become independent technical expert.
- Program complex non‑efficacy outputs/figures.
- Perform Senior Review and Deliver QC of non‑statistical output.
- Become involved in developing the standard macro library and take responsibility to implement standard macros within a study.
- Validate and perform User Acceptance Testing (UAT) on standard macros.
- Identify macros requirements, communicate and perform training.
- Create, QC and update complex dataset specifications (including efficacy) for single/multiple studies, ISS/ISEs, etc.
Qualifications
- Educated to BSc or above within Computer Science, Mathematics or a Science related discipline.
- SAS Programming Experience within the pharmaceutical industry.
- Good awareness of clinical trial issues, design, and implementation.
- Experience of regulatory submissions and associated industry guidance.
- Familiarity with GCP and regulatory requirements.
- Knowledge of SDTM and ADaM CDISC standards.
About Phastar
Phastar is an award‑winning biometrics and data science CRO, trusted by pharma, biotech, and medical device companies worldwide. With a global team of data specialists, we bring expertise, precision, and pace to every trial, because behind every data point is a patient waiting for treatment. We transform complex data into clear, actionable intelligence, helping accelerate drug development, and bring life‑changing therapies to patients faster.
Awards & Recognition
- SCRIP – Best Contract Research Organization, Specialist Provider.
- Citeline – 2025 Award Winner.
- Fierce CRO Awards – Recognized Industry Leader.
Be part of a team known for technical expertise, quality, and impact. We value Excellence, Collaboration, Integrity, Innovation, and Passion—and we seek team members who embody these qualities. Apply today!
Phastar is committed to the principles and practices of equal opportunities and to encourage the establishment of a diverse workforce. It is our policy to employ individuals on the basis of their suitability for the work to be performed and their potential for development, regardless of age, sex, race, color, nationality, ethnic or national origin, disability, marital status, pregnancy or maternity, sexual orientation, gender reassignment, religion, or belief. This includes creating a culture that fully reflects our commitment to equal opportunities for all.
Senior/Principal Statistical Programmer - FSP employer: PHASTAR
Contact Detail:
PHASTAR Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior/Principal Statistical Programmer - FSP
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to statistical programming. We recommend doing mock interviews with friends or using online platforms to get comfortable with articulating your experience and skills.
✨Tip Number 3
Showcase your expertise! Create a portfolio of your work, including any projects or datasets you've worked on. This will give potential employers a tangible sense of your skills and how you can contribute to their team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Senior/Principal Statistical Programmer - FSP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior/Principal Statistical Programmer role. Highlight your SAS programming experience and any relevant projects you've led. We want to see how your skills align with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your background in the pharmaceutical industry makes you a great fit. We love seeing genuine enthusiasm!
Showcase Your Technical Skills: Don’t forget to mention your knowledge of SDTM, ADaM, and regulatory submissions. We’re looking for someone who can hit the ground running, so make sure we know about your technical expertise right from the start.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates. Plus, it shows you’re keen to join our team!
How to prepare for a job interview at PHASTAR
✨Know Your Stats Inside Out
Make sure you brush up on your statistical programming knowledge, especially around SAS and CDISC standards like SDTM and ADaM. Be ready to discuss your experience with complex datasets and how you've validated them in past projects.
✨Familiarise Yourself with Regulatory Requirements
Since the role involves oversight of regulatory submissions, it’s crucial to understand FDA CRT requirements. Prepare to talk about your experience with define.xml and define.pdf, and how you’ve navigated GCP and other regulatory guidelines in your previous roles.
✨Showcase Your Leadership Skills
As a Senior/Principal Statistical Programmer, you'll be leading teams. Think of examples where you've successfully led projects or mentored others. Highlight your ability to communicate effectively and train team members on macros and dataset specifications.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare insightful questions about their projects, team dynamics, and how they embody their values of excellence and innovation. This shows your genuine interest in the role and helps you assess if it's the right fit for you.