At a Glance
- Tasks: Lead and support clinical trials using advanced SAS programming and data analysis.
- Company: Join a pioneering pharmaceutical company driving patient treatment innovation.
- Benefits: Fully remote work, continuous training, and a supportive team environment.
- Other info: Collaborative culture that values diversity and encourages intellectual curiosity.
- Why this job: Make a real impact in healthcare while working with cutting-edge technology.
- Qualifications: 8+ years of SAS programming experience in clinical trials and strong analytical skills.
The predicted salary is between 60000 - 80000 € per year.
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you will be at the heart of our client's innovation. As a Senior Statistical Programmer, you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
Position Overview
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.
Responsibilities
- Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
- Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
- Production and QC/validation programming
- Generating complex ad-hoc reports utilizing raw data
- Applying strong understanding/experience of Efficacy analysis
- Creating and reviewing submission documents and eCRTs
- Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
- Performing lead duties when called upon
- Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
- Being adaptable and flexible when priorities change
Qualifications
To be successful in this position you will have:
- Bachelor’s degree in one of the following fields: Statistics, Computer Science, Mathematics, etc.
- At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent.
- At least 6 years of related experience with a master’s degree or above.
- Study lead experience, preferably juggling multiple projects simultaneously preferred.
- Strong SAS data manipulation, analysis and reporting skills.
- Solid experience implementing the latest CDISC SDTM / ADaM standards.
- Strong QC/validation skills.
- Good ad-hoc reporting skills.
- Proficiency in Efficacy analysis.
- Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.
- Submissions experience utilizing define.xml and other submission documents.
- Experience supporting immunology, respiratory or oncology studies would be a plus.
- Excellent analytical & troubleshooting skills.
- Ability to provide quality output and deliverables, in adherence with challenging timelines.
- Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
Senior Statistical Programmer FSP (SAS+R) employer: Cytel
Cytel is an exceptional employer that empowers its employees to thrive in a collaborative and innovative environment, particularly for those in the Senior Statistical Programmer role. With a strong commitment to professional development and a fully remote work option, Cytel fosters a culture of intellectual curiosity and diversity, ensuring that every team member can contribute meaningfully to groundbreaking pharmaceutical advancements. Join us to be part of a dynamic team where your expertise will directly impact the future of patient treatment.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Statistical Programmer FSP (SAS+R)
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical and biotech industries. Attend relevant webinars or local meetups to meet potential employers and get your name out there.
✨Tip Number 2
Show off your skills! Create a portfolio showcasing your SAS programming projects, especially those related to clinical trials. This will give you an edge and demonstrate your expertise to potential employers.
✨Tip Number 3
Prepare for interviews by brushing up on common questions related to statistical programming and clinical trials. Practice articulating your experience with CDISC standards and how you've contributed to past projects.
✨Tip Number 4
Don’t forget to apply through our website! We’re always looking for talented individuals like you. Plus, it’s a great way to ensure your application gets the attention it deserves.
We think you need these skills to ace Senior Statistical Programmer FSP (SAS+R)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to highlight your SAS programming skills and experience with clinical trial data. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects or achievements!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to express your enthusiasm for the role and the company. Share why you’re excited about working in the pharmaceutical industry and how you can contribute to our client's innovation.
Showcase Your Technical Skills:Don’t forget to emphasise your technical expertise, especially in CDISC standards and Efficacy analysis. We love seeing candidates who can demonstrate their proficiency in SAS and how they’ve applied it in real-world scenarios.
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity!
How to prepare for a job interview at Cytel
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills before the interview. Be ready to discuss specific projects where you've used SAS for data manipulation and analysis, especially in clinical trials. Highlight your experience with CDISC standards like SDTM and ADaM, as this will show you're well-versed in industry requirements.
✨Showcase Your Problem-Solving Skills
Prepare to share examples of how you've tackled complex data challenges in previous roles. Think about times when you had to generate ad-hoc reports or validate datasets under tight deadlines. This will demonstrate your analytical abilities and your capacity to deliver quality results, even when the pressure is on.
✨Emphasise Team Collaboration
Since this role involves working closely with cross-functional teams, be ready to discuss your experience collaborating with others. Share instances where you’ve successfully communicated project specifications or resolved issues with team members. This will highlight your ability to work effectively in a globally dispersed environment.
✨Be Ready for Technical Questions
Expect some technical questions related to statistical programming and clinical trial processes. Brush up on your knowledge of efficacy analysis and the drug development life cycle. Being able to confidently answer these questions will show that you have the expertise needed for the role and are genuinely interested in the field.
