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- Tasks: Join a global pharmaceutical client as a Principal Statistical Programmer, driving innovation in patient treatment.
- Company: Cytel supports your journey within a leading pharmaceutical company focused on next-gen treatments.
- Benefits: Enjoy autonomy, ownership, and the chance to work on impactful projects in a collaborative environment.
- Why this job: Be part of a transformative programme that empowers you to make a real difference in healthcare.
- Qualifications: Bachelor's degree in relevant fields and 7+ years of statistical programming experience required.
- Other info: Ideal for those with SAS expertise and a passion for clinical development.
The predicted salary is between 48000 - 72000 £ per year.
Responsibilities
- Provide technical leadership in SAS programs and applications designed to analyze and report complex clinical trial data in Tables, Listings, and Figures, and for electronic submissions of SDTM, ADaM datasets in CDlSC format, with minimal instruction or input from supervisor
- Provide technical leadership to create, review, and approve documentation required to support data analysis, reporting, and CDlSC data submission
- Ensure compliance with company SOP\’S and FDA/ICH/GCP regulations
- Perform quality control checks of advanced SAS code for datasets and output produced by other statistical programmers
- Review, maintain study documents per standard process
- Program, test, and document global utility programs and tools in accordance with standards and validation procedures
- Conduct briefings and participate in technical meetings for internal and external representatives (e.g., IS, CROs, Clinical Development Partners, Software Vendors, FDA, EMA, et cetera) for projects
- Perform lead duties when called upon
- Perform other duties as assigned
Qualifications
- Technical and Communication Skills: Proven expert in all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH
- R programming experience is a plus
- Excellent and transparent communication skills and ability to interact across multiple functions
- Adaptability and flexibility for when priorities change
Education and Experience
- MS in biostatistics or a related field, with 8+ years of experience in pharmaceutical industry, or BS in biostatistics or a related field, with 10+ years of experience in pharmaceutical industry
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Principal Statistical Programmer FSP employer: Cytel
Contact Detail:
Cytel Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Statistical Programmer FSP
✨Tip Number 1
Familiarise yourself with CDISC standards, especially SDTM and ADaM. Understanding these standards will not only help you in your role but also demonstrate your expertise during interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, particularly those involved in clinical development. Attend relevant conferences or webinars to make connections that could lead to job opportunities.
✨Tip Number 3
Brush up on your SAS programming skills and consider learning additional languages like R or Python. Being proficient in multiple programming languages can set you apart from other candidates.
✨Tip Number 4
Stay updated on FDA regulations and guidelines related to clinical trials. This knowledge will be crucial in your role and will show potential employers that you are proactive and informed.
We think you need these skills to ace Principal Statistical Programmer FSP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in statistical programming, particularly with SAS and CDISC standards. Emphasise any relevant projects or roles that align with the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the pharmaceutical industry and your understanding of clinical development. Mention specific experiences that demonstrate your ability to work independently and lead projects.
Highlight Relevant Skills: In your application, clearly outline your exceptional SAS programming skills and any additional programming languages you are proficient in, such as R or Python. This will help you stand out as a candidate who can contribute to various aspects of the role.
Showcase Communication Abilities: Since outstanding communication skills are essential for this role, provide examples in your application of how you've effectively communicated complex statistical concepts to non-technical stakeholders or collaborated with cross-functional teams.
How to prepare for a job interview at Cytel
✨Showcase Your Technical Skills
As a Principal Statistical Programmer, your SAS programming skills are crucial. Be prepared to discuss specific projects where you've developed and validated SAS or R programs. Highlight your experience with CDISC standards and any complex datasets you've worked on.
✨Demonstrate Your Understanding of Regulations
Familiarise yourself with FDA regulations and good clinical practices. During the interview, be ready to explain how you ensure compliance in your work, especially regarding regulatory submissions and clinical trial data reporting.
✨Emphasise Collaboration Experience
This role involves working closely with CROs and other stakeholders. Share examples of how you've successfully collaborated with different teams to meet project timelines and goals, showcasing your communication and leadership skills.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities in real-world scenarios. Think about challenges you've faced in previous roles, particularly in statistical programming, and how you overcame them. This will demonstrate your critical thinking and adaptability.
