Vagas na beBeeStatistician em Brasil

Job Title: Clinical Statistical Programmer · Job Description · We are seeking a highly skilled Clinical Statistical Programmer to support clinical trial data standardization, analysis, and regulatory submissions. · Transform raw clinical trial data into CDISC-compliant SDTM and A ...

As a statistician in the field of clinical trials, you will play a key role in standardizing data through statistical analysis. · Transform raw clinical trial data into compliant formats using established methodologies · About You: · Familiarity with SAS programming is essential ...

Clinical Statistical Programmer Role · Job Title: Clinical Statistical Programmer (SAS / CDISC) · We are seeking a detail-oriented clinical statistical programmer to support clinical trial data standardization, analysis, and regulatory submissions. The ideal candidate will have s ...

Clinical Statistical Programmer · Are you a detail-oriented professional with expertise in CDISC standards, SAS programming and generation of Tables, Listings and Figures? We seek a skilled Clinical Statistical Programmer to support clinical trial data standardization, analysis a ...

Clinical Statistical Programmer · Transforming clinical trial data into CDISC-compliant SDTM and ADaM datasets is a crucial responsibility in this role. The successful candidate will work closely with cross-functional teams to develop efficient SAS programs, automate reporting ta ...

Clinical Statistical Programmer Position Overview · As a Clinical Statistical Programmer, you will be responsible for supporting clinical trial data standardization, analysis, and regulatory submissions. The ideal candidate should have strong expertise in CDISC standards (SDTM & ...

Job Overview · Clinical Statistical Programmer · We are seeking a detail-oriented statistician to support clinical trial data standardization, analysis and regulatory submissions in the life sciences industry. · Detailed understanding of statistical concepts, methods and techniqu ...

We are seeking a detail-oriented Clinical Data Analyst to support clinical trial data standardization, analysis, and regulatory submissions. · Key Responsibilities · Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets. · Develop, validate, and maintain T ...

Clinical Statistical Programmer Position · Collaborate with cross-functional teams to standardize clinical trial data, ensuring regulatory compliance and accuracy. · Develop statistical programming skills in SAS to create Tables, Listings, and Figures (TLFs) for clinical study re ...

Job Title: Clinical Statistical Programmer · 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 and gen ...

Clinical Statistical Programmer Job · We are seeking a skilled Clinical Statistical Programmer to support our 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 Job Summary · Our company is seeking a detail-oriented Clinical Statistical Programmer to support clinical trial data standardization, analysis, and regulatory submissions. · Develop, validate, and maintain Tables, Listings, and Figures (TLFs) for ...

**Clinical Statistical Programmer Position Summary** · We are seeking a detail-oriented and experienced Clinical Statistical Programmer to support clinical trial data standardization, statistical analysis, and regulatory submissions in Brazil. · Key Responsibilities: · Transform ...

Clinical Statistical Programmer Role Overview · We are seeking a skilled Clinical Statistical Programmer to support our clinical trial data standardization, statistical analysis, and regulatory submissions. · Transform raw clinical trial data into CDISC-compliant SDTM and ADaM da ...

Clinical Statistical Programmer Position Overview · The ideal candidate will play a key role in supporting clinical trial data standardization, statistical analysis, and regulatory submissions. · Key Responsibilities: · Transform raw clinical trial data into CDISC-compliant SDTM ...

Clinical Statistical Programmer: We are seeking an experienced data expert to support clinical trial data standardization, statistical analysis, and regulatory submissions. · This position requires strong expertise in SAS programming, CDISC standards (SDTM & ADaM), and the develo ...

Clinical Statistical Programmer Position · We are seeking a detail-oriented Clinical Statistical Programmer to support clinical trial data standardization, analysis, and regulatory submissions. This role is ideal for professionals with strong expertise in CDISC standards (SDTM & ...

We are seeking a detail-oriented statistician to support data standardization, analysis, and regulatory submissions in the pharmaceutical industry. The ideal candidate will have expertise in CDISC standards (SDTM & ADaM), programming languages like SAS and Python/R for data clean ...

Job Title: Statistical Programmer for Clinical Data Standardization · We are seeking a detail-oriented programmer to support clinical trial data standardization, analysis, and regulatory submissions. · About the Role: · The ideal candidate will have strong expertise in CDISC stan ...

Clinical Statistical Programmer Role · Our organization is 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 SAS progra ...