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- Tasks: Lead the design and development of SAS programs for clinical data analysis.
- Company: Join IQVIA, a global leader in clinical research and healthcare intelligence.
- Benefits: Enjoy a competitive salary, flexible working hours, and opportunities for professional growth.
- Why this job: Make a real impact on patient outcomes through innovative medical treatments.
- Qualifications: 5+ years in statistical programming with strong SAS skills and knowledge of CDISC standards.
- Other info: Work in a dynamic, multicultural team with excellent career advancement opportunities.
The predicted salary is between 36000 - 60000 £ per year.
The Senior Statistical Programmer will be responsible for reviewing datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses.
Main Responsibilities and Accountabilities:
- Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, Tables, Figures, Listings and Analysis Submission content.
- Collaborates with study teams to ensure the quality and accuracy – thus submission readiness – of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml).
- Leads and oversees requested efforts for pooled and exploratory analyses working closely with Statistics TA lead and/or study statisticians as well as with clinical programming team and their collection of legacy data.
- Leads and oversees the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO.
- Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format.
- Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group.
- Works closely with clinical study teams to plan and execute activities to ensure project timelines are met with high quality deliverables.
Additional tasks:
- Collaborates with CR&D staff regarding data analysis requests.
- Performs additional statistical analyses including but not limited to:
- support responses to regulatory agencies,
- generate integrated summary of safety and efficacy,
- support publications and presentations,
- support planning and reporting of clinical trials via exploratory analyses of available data.
Position Qualifications and Experience Requirements:
Education:
- BSc in Computer Science, Mathematics, Statistics or related area with relevant experience.
Experience:
- At least 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software.
- In-depth understanding of clinical programming and/or statistical programming processes and standards.
- In-depth understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH).
- Extensive experience with statistical programming using the SAS software including development and use of SAS Macros.
- Strong programming and problem-solving skills.
- Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM).
- Proven experience in leading programming activities for pooled and exploratory analyses across multiple clinical studies and submission activities (or equivalent).
- Proven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines.
- Experience in working in cross-functional, multicultural and international clinical trial teams.
Senior Statistical Programmer (FSP - Permanent Homebased) in Livingston employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Statistical Programmer (FSP - Permanent Homebased) in Livingston
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant meetups or webinars, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for those 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 talking about your experience with SAS and clinical data.
✨Tip Number 3
Showcase your skills! Create a portfolio of your work, including examples of SAS programs you've developed or projects you've led. This will give potential employers a tangible sense of your expertise 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 Statistical Programmer (FSP - Permanent Homebased) in Livingston
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience in statistical programming and clinical data analysis. We want to see how your skills align with the responsibilities mentioned in the job description, so don’t hold back on showcasing your SAS expertise!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Senior Statistical Programmer role. Share specific examples of your past work that demonstrate your ability to lead programming activities and ensure submission readiness.
Showcase Your Teamwork Skills: Collaboration is key in this role, so make sure to highlight your experience working with cross-functional teams. We love seeing candidates who can effectively communicate and work alongside study teams to deliver high-quality results.
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 get you one step closer to joining our team at StudySmarter!
How to prepare for a job interview at IQVIA
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills, especially around ADaM datasets and macros. Be prepared to discuss specific projects where you've used SAS to analyse clinical data, as this will show your hands-on experience.
✨Understand Regulatory Standards
Familiarise yourself with GCP, ICH, and CDISC standards. During the interview, be ready to explain how you've ensured compliance in past projects, as this demonstrates your understanding of the regulatory landscape.
✨Showcase Collaboration Skills
Since the role involves working closely with study teams, think of examples where you've successfully collaborated on projects. Highlight your ability to communicate effectively across different functions and cultures, as this is key in a global environment.
✨Prepare for Problem-Solving Questions
Expect questions that assess your problem-solving abilities, particularly in statistical programming. Prepare scenarios where you've tackled complex issues or improved processes, as this will showcase your analytical thinking and leadership skills.
