# Senior Statistical Programmer

**Company**: IQVIA
**Location**: Reading, Berkshire
**Work arrangement**: remote
**Experience**: senior
**Job type**: full-time
**Category**: Data Science
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Reading-Berkshire-United-Kingdom/Senior-Statistical-Programmer--FSP---Permanent-Homebased-_R1521995-2?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/senior-statistical-programmer-7631789f-2eb/

## 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 study teams to design data structure and specifications for ad hoc and study deliverables, including ADaM datasets, Tables, Figures, Listings, and Analysis Submission content.

- 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.

- Designs and implements complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format.

- Develops global tools that will increase the efficiency and capacity of the Statistical Programming group.

**Additional tasks:**

- Collaborates with CR&D staff regarding data analysis requests.

- Performs additional statistical analyses, including support responses to regulatory agencies, generating integrated summaries of safety and efficacy, supporting publications and presentations, and supporting planning and reporting of clinical trials via exploratory analyses of available data.

**Position Qualifications and Experience Requirements:**

- BSc in Computer Science, Mathematics, Statistics, or related area with relevant 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.

- Extensive experience with statistical programming using SAS software, including development and use of SAS Macros.

- Strong programming and problem-solving skills.

- Good experience in R Programming (trained/hands-on experience).

- 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.

**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.

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## Skills

### Required
- SAS
- R
- CDISC
- ADaM
- SDTM
- CDASH
- Statistical Programming
- Clinical Programming

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