The role
You will turn clinical data into the datasets, tables, listings and figures that a submission is built on — accurately, reproducibly, and on a timeline that never moves right.
What you will do
- Develop and validate SDTM and ADaM datasets to CDISC standards
- Produce tables, listings and figures for study reports and submissions
- Perform independent programming validation of colleagues' outputs
- Contribute to programming standards, macros and reusable tooling
- Support database lock and submission deliverables
What success looks like at 12 months
Your outputs pass validation first time, you have improved at least one shared standard or macro, and a database lock has run to schedule with your deliverables in it.
What we require
- Strong SAS programming; R is welcome alongside it
- Working knowledge of CDISC SDTM and ADaM standards
- Experience producing regulatory-grade outputs
- Precision under deadline pressure
What we would like, but will teach you
- Submission experience
- Experience building macros or automation for a programming team
- Exposure to define.xml and submission packages
If you meet the required list, apply. We cap the preferred list at four items on purpose, and we would rather read an application from someone who is 70% there and hungry.
Hybrid — onsite at Research Triangle Park, NC three days a week (Tuesday, Wednesday and one team-chosen day).
Pay and rewards
This role sits at grade 8, with a base range of $107,000 – $138,000 for this location, plus annual bonus, retirement contributions of up to 9%, and day-one benefits. See the full package.
About the site
Our clinical development and digital hub. More about our locations.
Accommodations
Need an adjustment to apply or interview? Email accommodations@ingenbiotech.example. It goes to a separate team and is never shared with the hiring manager. What we can arrange.
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