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