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Clinical Statistical Programmer · Job Title: Clinical Statistical Programmer (SAS / CDISC) · Location: Remote · Duration: Long Term Contract · We are seeking a detail-oriented professional to support clinical trial data standardization, analysis, and regulatory submissions. · The ...

Job Title: Statistical Data Programmer · We are seeking an experienced Clinical Statistical Programmer to join our team. The ideal candidate will play a key role in supporting clinical trial data standardization, statistical analysis, and regulatory submissions. · <h3 id= ...

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 generation of Tables, Listings, and Figures (T ...

Job Title: Statistical Data Analyst · Location: Remote · Job Description: · We are seeking a detail-oriented data analyst to support clinical trial data standardization, analysis, and regulatory submissions. The ideal candidate will have strong expertise in CDISC standards (SDTM ...

We are seeking a detail-oriented Clinical Statistical Programmer 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 m ...

Job Title: Clinical Statistical Programmer · About the Role: · 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 standard ...

**Clinical Data Specialist - Long Term Contract ** · We are seeking a detail-oriented and analytical Clinical Data Specialist to support clinical trial data standardization, analysis, and regulatory submissions. · Develop, validate, and maintain Tables, Listings, and Figures (TLF ...

Job Title: Statistical Programmer Specialist · We are seeking a detail-oriented and experienced professional to play a key role in supporting clinical trial data standardization, statistical analysis, and regulatory submissions. The ideal candidate will have strong expertise in S ...

We are seeking a detail-oriented Clinical Statistical Programmer to support clinical trial data standardization, analysis, and regulatory submissions. This role involves transforming raw clinical trial data into CDISC-compliant datasets, developing Tables, Listings, and Figures ( ...

Job Title: Clinical Statistical Programmer (SAS / CDISC) · We are seeking a detail-oriented professional to support clinical trial data standardization, analysis, and regulatory submissions. · SAS Programming: Strong experience with object-Oriented SAS programming paradigm, inclu ...

Clinical Statistical Programmer · Job Description: · Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets. · Key Skills and Qualifications · Strong experience with SAS programming. · , ...

Job Title: 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 for seamless integratio ...

Clinical Statistical Programmer · Job Description: · We are seeking a detail-oriented statistical programmer to join our team. As a clinical statistical programmer, you will be responsible for transforming raw data into CDISC-compliant datasets and developing reusable scripts for ...

Clinical Statistical Programmer · The Clinical Statistical Programmer is a detail-oriented professional with expertise in CDISC standards, SAS programming, and Table List Figure (TLF) generation. The role involves transforming raw clinical trial data into compliant datasets for r ...

Clinical Statistical Programmer · Job Summary: · 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 ...

Job Title: Clinical Statistical Programmer (SAS / CDISC) · Location: Remote · Duration: Long Term Contract · About the Role: · We are seeking a skilled Clinical Data Analyst to support clinical trial data standardization, analysis, and regulatory submissions. The ideal candidate ...

Clinical Statistical Programmer Job Opportunity · We are seeking a skilled Clinical Statistical Programmer to support clinical trial data standardization, analysis, and regulatory submissions. · Develop, validate, and maintain Tables, Listings, and Figures (TLFs) for clinical stu ...

Clinical Statistical Programmer Opportunity · Role: Clinical Statistical Programmer · Location: Remote or Brazil · We are seeking a detail-oriented and skilled clinical statistical programmer to support the standardization, analysis, and regulatory submission of clinical trial da ...

Clinical Statistical Programmer Role Overview · We are seeking a detail-oriented and experienced Clinical Statistical Programmer to support clinical trial data standardization, statistical analysis, and regulatory submissions. · ...

Clinical Data Specialist Position · Job Summary: · , ...