Vagas na beBeeDataStandardizer em Brasil

**Clinical Statistical Programmer Role Summary:** · Are you a detail-oriented individual with strong expertise in CDISC standards, SAS programming, and data analysis? We are seeking a Clinical Statistical Programmer to support clinical trial data standardization, analysis, and re ...

**Clinical Statistical Programmer Role Summary** · We are seeking a detail-oriented professional to support clinical trial data standardization, analysis, and regulatory submissions. · The ideal candidate will have strong expertise in CDISC standards (SDTM & ADaM), SAS programmin ...

Clinical Statistical Programmer · Job Description: · 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 & ...

Clinical Data Standardization Expert · We are seeking an experienced Clinical Data Standardization Expert to support clinical trial data standardization, analysis, and regulatory submissions. · The ideal candidate will have strong expertise in CDISC standards (SDTM & ADaM), SAS p ...

We are seeking a detail-oriented Clinical Statistical Programmer to support clinical trial data standardization, analysis, and regulatory submissions. · Key Responsibilities: · Develop, validate, and maintain Tables, Listings, and Figures (TLFs) for clinical study reports and re ...

Clinical Data Standardization Expert · Role Description: · We are seeking a highly skilled Clinical Statistical Programmer to support the standardization, analysis, and regulatory submission of clinical trial data. The ideal candidate will have strong expertise in CDISC standards ...

Clinical Statistical Programmer Role · We are seeking an experienced clinical statistical programmer to support our team in Brazil. The ideal candidate will play a key role in standardizing clinical trial data, conducting statistical analysis, and preparing regulatory submissions ...

Clinical Statistical Programmer Role · This is a detail-oriented position that involves supporting clinical trial data standardization, analysis, and regulatory submissions. · Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets. · Develop, validate, and ...

**Clinical Statistical Programmer Role Summary** · We are seeking a detail-oriented professional to support clinical trial data standardization, analysis, and regulatory submissions. The ideal candidate will have strong expertise in CDISC standards (SDTM & ADaM), SAS programming, ...

Clinical Statistical Programmer Opportunity · Job Title: Clinical Statistical Programmer (SAS / CDISC) · Location - Brazil · Role Summary · We are seeking a detail-oriented clinical statistical programmer to support clinical trial data standardization, analysis, and regulatory s ...

Clinical Statistical Programmer · We are seeking a detail-oriented professional to support clinical trial data standardization, analysis and regulatory submissions. · Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets using advanced statistical techniqu ...

Clinical Statistical Programmer Role Overview · This role involves leveraging expertise in CDISC, SAS, and TLFs to facilitate clinical trial data standardization. · ...

Job Title: Clinical Statistical Programmer (SAS / CDISC) · Transform raw clinical trial data into standardized datasets · Develop, validate, and maintain Tables, Listings, and Figures (TLFs) for clinical study reports and regulatory submissions · Create efficient SAS programs for ...

Job Title: Data Standardization Specialist · We are seeking a detail-oriented professional to support the standardization of clinical trial data. · About This Role · This position is responsible for transforming raw clinical trial data into CDISC-compliant datasets and developing ...

**Clinical Statistical Programmer Role**: We are seeking a detail-oriented professional to support clinical trial data standardization, analysis, and regulatory submissions. · Key Responsibilities: · Support data standardization and analysis for clinical trials · Maintain experti ...