Vagas na Highbrow Technology Inc em Brasil

Clinical Statistical Programmer · At Highbrow Technology Inc., we are seeking a detail-oriented Clinical Statistical Programmer to support clinical trial data standardization analysis regulatory submissions. · Key Responsibilities: · Data Standardization: · TLF Generation: · SA ...

Clinical Statistical Programmer (SAS/CDISC) · Location: Brazil · ...

Clinical Statistical Programmer · A detail-oriented Clinical Statistical Programmer is needed to support clinical trial data standardization, analysis, and regulatory submissions. · Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets. · Develop, validate ...

Key Responsibilities: · Transform Clinical Trial Data into compliant datasets using CDISC standards. · Strong experience with SAS programming · , Interested candidates should possess hands-on experience generating TLFs for regulatory submissions. · ...

Clinical Statistical Programmer Role · SAS Programming: Utilize advanced techniques such as macro functions,data manipulation with statistical packages. · Data Analysis: Extract meaningful insights from high volumes of databases ,coding mistakes: · ...

Clinical Statistical Programmer · We are seeking a detail-oriented Clinical Statistical Programmer to support clinical trial data standardization, analysis, and regulatory submissions at Highbrow Technology Inc. · Transform raw clinical trial data into CDISC-compliant SDTM and AD ...

Clinical Statistical Programmer Role Summary · Transform raw clinical trial data into CDISC-compliant SDTM & ADaM datasets. · -Develop, validate, andTables, · Listings,and · Fictures(TLF)for Clinical Study Reports And Regulatory Submissions! · PfOgrm QAQC PerRFORMancE Troublesho ...

Clinical Statistical Programmer · A detail-oriented Clinical Statistical Programmer will support clinical trial data standardization, analysis, and regulatory submissions. · ...

About the Job: · The role requires strong expertise in SAS programming, CDISC standards (SDTM & ADaM). Candidates should have experience generating Tables Listsings& Figures (TLFs) for regulatory submisisons. · Key Responsibilities:<ol style= ...

Clinical Statistical Programmer · At Highbrow Technology Inc., we seek a detail-oriented Clinical Statistical Programmer to support clinical trial data standardization. · Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets. · Develop Tables, Listings, an ...

Clinical Statistical Programmer · Develop, validate, and maintain Tables Listings Figures (TLFs) for clinical study reports. · Edit write efficient well documented SAS programs for data cleaning derivations reporting . · ...

Clinical Statistical Programmer · We are seeking a detail-oriented Clinical Statistical Programmer at Highbrow Technology Inc. · Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets. · Develop, validate, and maintain Tables, Listings, and Figures (TLFs) f ...

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

Job Description · A detail-oriented Clinical Statistical Programmer supports clinical trial data standardization, analysis, and regulatory submissions using CDISC standards (SDTM & ADaM), SAS programming. · ,(Develops Tables Listings Figures TLFs) for clinical study reports and r ...

Clinical Statistical Programmer Job Description: · We are seeking a highly skilled Clinical Statistical Programmer to join our team at Highbrow Technology Inc. · The role involves working on various projects related to clinical trials including preparing study reports for regulat ...

We are seeking a detail-oriented Clinical Statistical Programmer to support clinical trial data standardization · and regulatory submissions at Highbrow Technology Inc. · Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets using strong expertise in SAS p ...

Job Description: · Develop validate maintain TLFs tables listings figures CLINICAL STUDY REPORTS REGULATORY SUBMISSIONS · Write efficient well-documented SAS programs clean derivations report high-quality results. · ...

Clinical Statistical Programmer Role · Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets. · Develop, · validate, · and maintain Tables,Listings,and Figures (TLFs) for clinical study reports and regulatory submissions. · Write efficient, · well-document ...

Clinical Statistical Programmer Job Description · We are seeking a detail-oriented Clinical Statistical Programmer to work on our team at Highbrow Technology Inc. · supportauditsregulatoryinspectionsreproducibledocuments. · h4-Requir edQualification: · i.-strongexperincewithsaspr ...

Clinical Statistical Programmer · Job Summary: · We are seeking a detail-oriented Clinical Statistical Programmer to support clinical trial data standardization, analysis, and regulatory submissions. · ...