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- Tasks: Lead statistical programming for clinical trials and ensure data quality for submissions.
- Company: Join IQVIA, a global leader in clinical research and healthcare intelligence.
- Benefits: Enjoy remote work, great work/life balance, and career advancement opportunities.
- Why this job: Make a real impact on healthcare by working with top pharmaceutical companies.
- Qualifications: 5+ years in statistical programming with SAS; strong problem-solving skills required.
- Other info: Collaborative team environment with diverse therapeutic areas and long-term engagement.
The predicted salary is between 48000 - 84000 £ per year.
Join to apply for the Senior Statistical Programmer (FSP - Permanent Homebased) role at IQVIA. This role will be dedicated to one of IQVIA’s largest clients through a Functional Service Provider (FSP) type partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech companies offering you a unique opportunity to work on a team where your role is both challenging and rewarding, while working alongside colleagues who are passionate about influencing the future of medicine and advancing therapies. With IQVIA's FSP business unit, you become a core part of a dynamic team dedicated to reshaping the future of healthcare.
Additional Benefits
- Home-based remote work opportunities
- Great work/life balance
- Collaborate on projects and innovations with industry leaders in the Pharma and CRO sectors
- Cohesive team environment fostering a collaborative approach to study work
- Variety of therapeutic areas, indications and study phases
- Job stability; long-term engagements and development opportunities
- Career advancement opportunities
Job Description
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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Senior Statistical Programmer (FSP - Permanent Homebased) employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Statistical Programmer (FSP - Permanent Homebased)
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at IQVIA or similar companies. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your SAS skills and understanding CDISC standards. We recommend practising common interview questions related to statistical programming and clinical data analysis to show you're ready to hit the ground running.
✨Tip Number 3
Showcase your experience with real-world examples during interviews. Talk about specific projects where you led programming activities or collaborated with study teams. This will help us see how you can contribute to our dynamic team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re genuinely interested in joining our team at IQVIA.
We think you need these skills to ace Senior Statistical Programmer (FSP - Permanent Homebased)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Statistical Programmer role. Highlight your experience with SAS software and any relevant projects you've worked on. We want to see how your skills match 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 makes you a great fit. We love seeing enthusiasm and a personal touch.
Showcase Your Experience: In your application, be sure to showcase your experience in clinical programming and statistical programming. Mention specific projects or achievements that demonstrate your expertise in ADaM datasets and regulatory requirements.
Apply Through Our Website: Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy to do!
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 in relation to ADaM datasets and CDISC standards. Be prepared to discuss specific projects where you've used SAS to analyse clinical data, as this will show your expertise and experience in the field.
✨Understand Regulatory Requirements
Familiarise yourself with GCP and ICH guidelines relevant to statistical programming. During the interview, be ready to explain how you've ensured compliance in past projects, as this demonstrates your understanding of the industry's standards and your ability to deliver submission-ready data.
✨Showcase Your Collaboration Skills
Since the role involves working closely with study teams, think of examples where you've successfully collaborated with others. Highlight your experience in leading programming activities and how you’ve contributed to team success, as this will resonate well with their emphasis on a cohesive team environment.
✨Prepare for Problem-Solving Questions
Expect questions that assess your problem-solving abilities, particularly in complex programming scenarios. Prepare to discuss challenges you've faced in previous roles and how you overcame them, showcasing your analytical thinking and adaptability in a fast-paced environment.
