Master CDISC standards (SDTM, ADaM), electronic data capture (EDC) systems, trial management workflows, and 21 CFR Part 11 compliance to enable efficient multi-site clinical research.
Clinical trial software encompasses the digital infrastructure to run multi-site, regulated clinical studies: electronic case report forms (eCRF), randomization systems, adverse event tracking, and statistical analysis platforms. Most work orbits CDISC standards (SDTM, ADaM) mandated by FDA for regulatory submission. Core responsibilities:
| 지역 | 주니어 | 미들 | 시니어 |
|---|---|---|---|
| USA | — | — | — |
| UK | — | — | — |
| EU | — | — | — |
커리어 매칭을 해보세요 — 맞는 방향을 제안해 드립니다.
나에게 맞는 스킬 찾기 →2,536개 직무를 스킬 기반으로 매칭. 무료, 약 2분.
커리어 매칭 무료로 하기 →