Jobs at Pinnacle Engineering Group

This senior-level role places a statistical programmer fully embedded within a global pharmaceutical client's team, supported by Cytel's internal resources. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards like SDTM and ADaM. Key responsibilities include generating and validating statistical deliverables, performing complex data manipulation for efficacy and safety analysis, and creating submission documents. The role appeals to candidates seeking autonomy and ownership in a culture that values scientific rigor, innovation, and collaboration. It is a hybrid position requiring three days of on-site work in Pennsylvania or New Jersey, offering opportunities for professional growth through consistent training and development.

This senior-level role involves embedding within a global pharmaceutical client to lead statistical programming for early and late-stage clinical trials. The position requires advanced SAS expertise to generate and validate CDISC-compliant deliverables, including SDTM, ADaM, and efficacy analysis datasets, while managing complex ad-hoc reporting and submission documents. Key responsibilities include developing global programming standards, performing data manipulation for safety and pharmacokinetic studies, and collaborating with cross-functional teams to ensure project success. The opportunity is appealing due to the autonomy and ownership granted to employees, a culture that values scientific rigor and innovation, and access to consistent training and development. The work arrangement is hybrid, requiring three days per week on-site in Pennsylvania or New Jersey.

This senior statistical programmer role places the candidate fully embedded within a global pharmaceutical client's team, supported by Cytel's resources. The position focuses on leading statistical programming for early and late-stage clinical trials across various therapeutic areas. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data manipulation and analysis for efficacy and safety, and creating submission-ready documents using SAS and CDISC standards. The role appeals to professionals seeking autonomy and ownership in a culture that values scientific rigor, innovation, and collaboration. It offers a hybrid work arrangement requiring three days per week on-site in Pennsylvania or New Jersey, with opportunities for professional growth through consistent training and development.

This senior-level role places a statistical programmer fully embedded within a global pharmaceutical client's team, supported by Cytel's internal resources. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex efficacy and safety data analysis, and creating submission-ready documents. The role appeals to candidates seeking autonomy and ownership in a culture that values scientific rigor, innovation, and intellectual curiosity. It offers a hybrid work arrangement requiring three days per week on-site in Pennsylvania or New Jersey, with opportunities for professional growth through consistent training and development.

This senior statistical programmer role places the candidate fully embedded within a global pharmaceutical client's team, supported by Cytel's resources. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data analysis for efficacy and safety, creating submission documents, and developing global programming standards. The role is appealing due to the autonomy, ownership, and collaborative culture that values scientific rigor and innovation. It offers opportunities for professional growth through consistent training and development. The work arrangement is hybrid, requiring three days per week on-site in Pennsylvania or New Jersey.

This senior statistical programmer role places the candidate fully embedded within a global pharmaceutical client's team, supported by Cytel's resources. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data analysis for efficacy and safety, creating submission documents, and developing global programming standards. The role is hybrid, requiring three days per week on-site in Pennsylvania or New Jersey. It appeals to professionals seeking autonomy and ownership in a culture that values scientific rigor, innovation, and collaboration. The position offers opportunities for professional growth through consistent training and the chance to work on cutting-edge patient treatment initiatives.

This senior statistical programmer role places the candidate fully embedded within a global pharmaceutical client's team, supported by Cytel's internal resources. The position focuses on leading or supporting early and late-stage clinical trials across various therapeutic areas, including oncology. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data manipulation and efficacy analysis using SAS, and creating submission-ready documents and ad-hoc reports. The role appeals to professionals seeking autonomy and ownership in a culture that values scientific rigor, innovation, and collaboration. The position is hybrid, requiring three days per week on-site in Pennsylvania or New Jersey, with opportunities for professional growth through consistent training and development.

This senior statistical programmer role is embedded within a global pharmaceutical client's team, focusing on early and late-stage clinical trials. The position requires advanced SAS programming skills to generate and validate CDISC-compliant deliverables, including SDTM, ADaM, and TFLs, while performing complex data manipulation and efficacy analysis. Key responsibilities include creating submission documents, conducting quality control, and collaborating with cross-functional teams to support drug development. The role offers a hybrid work arrangement in Pennsylvania or New Jersey, three days on-site. It is appealing for its autonomy, ownership of projects, and access to consistent training and development within a culture that values scientific rigor, innovation, and intellectual curiosity.

This senior statistical programmer role is a hybrid position based in Pennsylvania or New Jersey, embedding the candidate within a global pharmaceutical client's team. The individual will leverage advanced SAS programming and CDISC standards to lead or support early and late-stage clinical trials across various therapeutic areas. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex efficacy and safety data analysis, creating submission documents, and developing global programming standards. The position is appealing for its focus on innovation, intellectual curiosity, and the opportunity to work autonomously on cutting-edge patient treatments. The role offers a collaborative culture with strong support for professional development and training, requiring eight years of industry experience in clinical trial data programming.

This senior statistical programmer role places the candidate fully embedded within a global pharmaceutical client's team, supported by Cytel's resources. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data analysis for efficacy and safety, creating submission documents, and developing global programming standards. The role appeals to professionals seeking autonomy and ownership in a culture that values scientific rigor, innovation, and collaboration. It offers a hybrid work arrangement requiring three days per week on-site in Pennsylvania or New Jersey, with opportunities for professional growth through consistent training and development.

This senior statistical programmer role is a sponsor-dedicated position embedded within a global pharmaceutical client, supporting early and late-stage clinical trials. The position requires advanced SAS programming skills to generate and validate CDISC-compliant deliverables, including SDTM, ADaM, and TFLs, while performing complex data manipulation and efficacy analysis. Key responsibilities include creating submission documents, conducting quality control, and collaborating with cross-functional teams to ensure project success. The role offers a hybrid work arrangement requiring three days on-site in Pennsylvania or New Jersey. It is appealing for its focus on innovation, intellectual curiosity, and the opportunity to work autonomously on cutting-edge patient treatments within a supportive, collaborative culture that values scientific rigor and professional development.

This senior-level role places a statistical programmer fully embedded within a global pharmaceutical client's team, supported by Cytel. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data analysis for efficacy and safety, and creating submission documents. The role appeals to candidates seeking autonomy and ownership in a culture that values scientific rigor, innovation, and collaboration. The work arrangement is hybrid, requiring three days per week on-site in Pennsylvania or New Jersey.

This senior statistical programmer role is a hybrid position based in Pennsylvania or New Jersey, embedding the candidate within a global pharmaceutical client to support early and late-stage clinical trials. The individual will leverage advanced SAS programming skills and CDISC standards to generate, validate, and review complex deliverables including SDTM, ADaM datasets, and efficacy analysis reports. Key responsibilities include performing data manipulation for safety and efficacy, creating submission documents, and leading programming standards development. The position appeals to professionals seeking autonomy and ownership within a culture that values scientific rigor, innovation, and intellectual curiosity. It offers opportunities for professional growth through consistent training and the chance to work on cutting-edge patient treatment initiatives in a collaborative, cross-functional environment.

This senior statistical programmer role is a sponsor-dedicated position embedded within a global pharmaceutical client, supporting early and late-stage clinical trials. The position requires advanced SAS programming skills to generate and validate CDISC-compliant deliverables, including SDTM, ADaM, and complex efficacy and safety reports. Key responsibilities involve performing data manipulation, developing global programming standards, creating submission documents, and collaborating with cross-functional teams. The role offers a hybrid work arrangement in Pennsylvania or New Jersey, three days on-site. It is appealing for its focus on innovation, intellectual curiosity, and the opportunity to work autonomously on cutting-edge patient treatment research within a supportive culture that values scientific rigor and professional development.

This senior statistical programmer role places the candidate fully embedded within a global pharmaceutical client's team, supported by Cytel's resources. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data analysis for efficacy and safety, creating submission documents, and developing global programming standards. The role appeals to professionals seeking autonomy and ownership in a culture that values scientific rigor, innovation, and collaboration. It offers a hybrid work arrangement requiring three days per week on-site in Pennsylvania or New Jersey, with opportunities for professional growth through consistent training and development.

This senior statistical programmer role is embedded within a global pharmaceutical client, focusing on early and late-stage clinical trials in the pharmaceutical and biotech sectors. The position requires advanced SAS programming expertise to generate and validate CDISC-compliant deliverables, including SDTM, ADaM, and complex efficacy and safety reports. Key responsibilities involve data manipulation, PK/PD modeling, creating submission documents, and leading quality control processes. The role offers a hybrid work arrangement in Pennsylvania or New Jersey, combining three days of on-site collaboration with remote flexibility. It appeals to candidates seeking autonomy and ownership within a culture that values scientific rigor, innovation, and intellectual curiosity, supported by consistent professional development and a collaborative global team environment.

This senior statistical programmer role places the candidate fully embedded within a global pharmaceutical client's team, supported by Cytel's resources. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data analysis for efficacy and safety, creating submission documents, and developing global programming standards. The role appeals to professionals seeking autonomy and ownership in a culture that values scientific rigor, innovation, and collaboration. It offers a hybrid work arrangement requiring three days on-site in Pennsylvania or New Jersey, with opportunities for professional growth through consistent training and development.

This senior statistical programmer role is a sponsor-dedicated position embedded within a global pharmaceutical client, supporting early and late-stage clinical trials. The position requires advanced SAS programming skills to generate and validate CDISC-compliant deliverables, including SDTM, ADaM, and TFLs, while performing complex data manipulation and efficacy analysis. Key responsibilities include creating submission documents, conducting quality control, and collaborating with cross-functional teams to ensure data integrity. The role offers a hybrid work arrangement in Pennsylvania or New Jersey, three days on-site. It is appealing for its focus on innovation, intellectual curiosity, and the opportunity to work autonomously on cutting-edge patient treatments within a supportive environment that values scientific rigor and professional growth.

This senior statistical programmer role places the candidate fully embedded within a global pharmaceutical client's team, supported by Cytel's resources. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data manipulation for efficacy and safety analyses, and creating submission-ready documents. The role appeals to professionals seeking autonomy and ownership in a culture that values scientific rigor, innovation, and collaboration. It offers a hybrid work arrangement requiring three days per week on-site in Pennsylvania or New Jersey, with opportunities for professional growth through consistent training and development.

This senior-level statistical programming role places the candidate fully embedded within a global pharmaceutical client's team, supported by Cytel's internal resources. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex efficacy and safety data analysis, and creating submission-ready documentation. The role appeals to professionals seeking autonomy and ownership in a culture that values scientific rigor, innovation, and intellectual curiosity. It offers a hybrid work arrangement requiring three days per week on-site in Pennsylvania or New Jersey, with opportunities for professional growth through consistent training and development.

This senior statistical programmer role places the candidate fully embedded within a global pharmaceutical client's team, supported by Cytel's resources. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex data analysis for efficacy and safety, creating submission documents, and developing global programming standards. The role appeals to professionals seeking autonomy and ownership in a culture that values scientific rigor, innovation, and collaboration. It offers a hybrid work arrangement requiring three days per week in Pennsylvania or New Jersey, with opportunities for professional growth through consistent training and development.

This senior-level role places a statistical programmer fully embedded within a global pharmaceutical client's team, supported by Cytel's internal resources. The position focuses on leading or supporting early and late-stage clinical trials using advanced SAS programming and CDISC standards. Key responsibilities include generating and validating SDTM and ADaM datasets, performing complex efficacy and safety data analysis, and creating submission-ready documents. The role appeals to candidates seeking autonomy and ownership in a culture that values scientific rigor, innovation, and intellectual curiosity. The work arrangement is hybrid, requiring three days per week on-site in Pennsylvania or New Jersey, with opportunities for professional growth through consistent training and development.

This senior statistical programmer role involves working fully embedded within a global pharmaceutical client's team to support early and late-stage clinical trials. The position requires leveraging advanced SAS programming skills to generate and validate CDISC-compliant deliverables, including SDTM and ADaM datasets, as well as performing complex efficacy and safety analyses. Key responsibilities include developing global programming standards, creating submission documents, and collaborating with cross-functional teams to ensure data integrity. The opportunity is appealing due to the autonomy and ownership granted to employees, the chance to drive innovation in patient treatment, and a culture that values scientific rigor and intellectual curiosity. The role is hybrid, requiring three days of on-site work in Pennsylvania or New Jersey, with strong support and development resources provided by the parent organization.