At a Glance
- Tasks: Lead and support clinical trials using advanced SAS programming and CDISC standards.
- Company: Join a global pharmaceutical client driving innovative patient treatments.
- Benefits: Fully remote work, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment 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; strong analytical skills required.
The predicted salary is between 36000 - 60000 £ per year.
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.
How you will contribute:
- 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:
- 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.
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll 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.
We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery. We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities. We prize innovation and seek intelligent solutions using leading-edge technology.
Senior Statistical Programmer FSP in Westminster employer: Cytel - EMEA
Cytel is an exceptional employer that fosters a culture of innovation and collaboration, empowering employees to take ownership of their work while supporting groundbreaking advancements in patient treatment. With a fully remote work option, we offer flexibility and a commitment to employee growth through continuous learning and diverse project opportunities, making it an ideal environment for Senior Statistical Programmers looking to make a meaningful impact in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Statistical Programmer FSP in Westminster
✨Network Like a Pro
Get out there and connect with folks in the industry! Attend conferences, webinars, or local meetups related to clinical trials and statistical programming. You never know who might have the inside scoop on job openings or can refer you directly.
✨Show Off Your Skills
When you get the chance to chat with potential employers, don’t hold back! Share specific examples of your SAS programming projects, especially those involving SDTM and ADaM datasets. This is your time to shine and demonstrate how you can add value to their team.
✨Tailor Your Approach
Before any interview, do your homework! Research the company’s recent projects and challenges in the pharmaceutical space. Tailor your responses to show how your experience aligns with their needs, especially in areas like efficacy analysis and QC validation.
✨Apply Through Our Website
Don’t forget to check out our website for the latest job openings! Applying directly through us not only gives you a better chance but also keeps you in the loop about new opportunities that match your skills in statistical programming.
We think you need these skills to ace Senior Statistical Programmer FSP in Westminster
Some tips for your application 🫡
Show Off Your SAS Skills:Make sure to highlight your advanced SAS programming skills in your application. We want to see how you've used these skills in real-world scenarios, especially in clinical trials. Don't hold back on the details!
CDISC Standards are Key:Since we're all about CDISC standards like SDTM and ADaM, be sure to mention your experience with these in your application. We love seeing candidates who can demonstrate their understanding and implementation of these standards.
Tailor Your Application:Take a moment to tailor your application to our job description. Use the same language and keywords we’ve included. This shows us you’ve done your homework and understand what we’re looking for.
Apply Through Our Website:We encourage you to apply through our website for a smoother process. It’s the best way for us to keep track of your application and ensure it gets the attention it deserves. Plus, it’s super easy!
How to prepare for a job interview at Cytel - EMEA
✨Master Your SAS Skills
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 any experience with SDTM and ADaM standards, as this will show you're well-versed in the requirements of the role.
✨Know Your Clinical Trials Inside Out
Familiarise yourself with the phases of clinical trials and the drug development life cycle. Be prepared to talk about your experience with safety and efficacy analyses, and how you've contributed to generating submission documents. This knowledge will demonstrate your expertise and commitment to the field.
✨Showcase Your Team Player Attitude
Since this role involves working closely with cross-functional teams, be ready to share examples of how you've collaborated effectively in the past. Discuss any leadership experiences or times when you went the extra mile to meet deadlines, as this will highlight your adaptability and teamwork skills.
✨Prepare for Ad-Hoc Reporting Questions
Expect questions about your experience with generating complex ad-hoc reports. Think of specific instances where you've had to analyse raw data and present findings. Being able to articulate your thought process and the tools you used will set you apart from other candidates.
