# Sr. Statistical Programmer (Sponsor dedicated)

**Company**: Syneos Health
**Location**: BRA-Remote
**Work arrangement**: remote
**Experience**: senior
**Job type**: full-time
**Category**: Data Science
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/BRA-Remote/Sr-Statistical-Programmer--Sponsor-dedicated----Experience-in-clinical-trials-working-with-SAS-and-R-programming---Brazil-Home-Based_25113708?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_f7c288fd-21c

## Description

We are seeking a Sr. Statistical Programmer (Sponsor dedicated) to join our team.

Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success.

**Job Responsibilities**

- Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications.

- Works to ensure that outputs meet quality standards and project requirements.

- Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs ensuring inspection readiness.

- Manages scheduling and time constraints across multiple projects at a time, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload.

- Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others.

- Acts as the lead statistical programmer.

- Participates in sponsor meetings, kickoff meetings, and bid defense meetings as statistical programming representative, as required by sponsor.

- Conducts effective internal meetings.

- Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business.

**R programming for clinical trials**

- Hands-on experience using R in clinical trial programming, including tidyverse packages (dplyr, tidyr, purrr, stringr, lubridate) for data manipulation, and familiarity with reproducible workflows in RStudio/Posit, Quarto/R Markdown and Git-based version control.

**Pharmaverse and CDISC tools**

- Working knowledge of pharmaverse packages, including admiral (ADaM derivations), submission-ready datasets and cards/cardx (Analysis Results Data, ARD).

- Experience with table, listing and figure tools such as gtsummary, rtables or Tplyr.

**Qualifications**

- Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of degree, an equivalent combination of education and demonstrated programming experience.

- Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.

- Excellent written and verbal communication skills.

- Ability to read, write, speak and understand English.

**Benefits**

- Career development and progression

- Supportive and engaged line management

- Technical and therapeutic area training

- Peer recognition and total rewards program

- Inclusive culture

## Skills

### Required
- SAS
- R
- clinical trials
- tidyverse
- pharmaverse
- CDISC
- gtsummary
- rtables
- Tplyr

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/BRA-Remote/Sr-Statistical-Programmer--Sponsor-dedicated----Experience-in-clinical-trials-working-with-SAS-and-R-programming---Brazil-Home-Based_25113708?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)