한국어·English
Veeva Systems company · OPEN ROLE
- Company
- Supports pharma and biotech companies' quality, clinical, and sales work with cloud software.
- Role
- Writes the code needed for clinical trial supply logistics systems directly.
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What you will do
We rewrote the responsibilities and qualifications in plain language instead of copying the original posting.
Responsibilities
- Study customer requirements and turn them into workable RTSM designs.
- Set up demos and lead design review meetings with customers.
- Write, test, debug, and deploy code for new and existing RTSM projects.
- Guide customers on RTSM practices that speed up their clinical trials.
- Keep program logic consistent and set up checks for operational control.
- Track timelines across several RTSM projects at once.
What you need
- Have 5+ years of experience with RTSM or IRT systems.
- Hold a four-year degree or equivalent industry experience.
Good to have
- Can code in C#, ASP.NET, XML, HTML, CSS, and JavaScript.
- Have knowledge of MSSQL.
- Have experience working with an RTSM vendor.
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Checked 2026-10-19
Veeva SystemsSenior Consultant - RTSMStart a mock application