- We are seeking a detail-oriented Clinical Statistical Programmer to support clinical trial data standardization, analysis, and regulatory submissions.
- The ideal candidate will have strong expertise in CDISC standards (SDTM & ADaM), SAS programming, and generation of Tables, Listings, and Figures (TLFs), along with experience in quality control and submission readiness.
- SAS programming.
- CDISC standards (SDTM &< i >ADaM).
”, “, “““Experience supporting FDA/EMA regulatory submissions preferred. Prior experience in a Pharma/Biotech/CRO environment also advantageous.”]””,”En”)”, ” regulated campaigns favourable therapeutic applications… },
Statistical Data Enthusiast - João Pessoa - beBeeDataStandardizer
Título do emprego: Clinical Statistical Programmer
Descrição
Clinical Statistical Programmer
Job Description: