What are the responsibilities and job description for the Statistical Programmer I position at Katalyst HealthCares & Life Sciences?
Responsibilities
Provides SAS programming support to all clinical studies.
Manages assigned programming CROs providing oversight and appropriate QC for programming deliverables.
Provide statistical programming support for regulatory submissions (e.g., FDA, EMA), including electronic submission standards (eCTD).
Provides primary programming and QC support for any internally produced outputs.
Reviews and approves SAS programming instructions and CDISC/ADaM specifications.
Performs statistical analysis and simulations using SAS to support clinical trial design and data interpretation.
Reviews and provides input on eCRF design, external vendor data specifications, edit checks, and other Data Management related documents to ensure appropriate data collection for statistical programming.
Works closely with biostatisticians and data managers to identify data issues and generate queries that may impact statistical analysis and/or programming.
Works closely with biostatisticians and other functions (Pharmacovigilance, Clinical Development, etc.) to support data review for internal stakeholders.
Assists with ensuring consistency across programming methods in similar studies within a program.
Requirements
Bachelor's degree or master's degree or higher in statistics, biostatistics, or other closely related discipline with a minimum of 8 years of relevant experience in the pharmaceutical/biotechnology industry.
Experience in applying clinical trial and statistical methodology to a variety of studies and indications across various phases of clinical development.
Knowledge of pharmaceutical and regulatory requirements, procedures, and policies.
Experience With BLA Or NDA/sNDA Submissions Is Required.
Knowledge of GCP, ICH, 21 CFR part 11, and other Guidance documents and policies related to clinical trials operations requirements.
In depth knowledge of CDISC and ADaM data set structures and requirements.
Proficiency with SAS programming skills to including knowledge of SAS ODS graphical procedures such as PROC SGPLOT and the graphics template language (GTL) Knowledge of all aspects of clinical drug development (Phase 1-4).
Experience working with a CRO partner.
Excellent computer skills; strong verbal and written communication skills
Ability to work well in a team environment as a contributor.
Provides SAS programming support to all clinical studies.
Manages assigned programming CROs providing oversight and appropriate QC for programming deliverables.
Provide statistical programming support for regulatory submissions (e.g., FDA, EMA), including electronic submission standards (eCTD).
Provides primary programming and QC support for any internally produced outputs.
Reviews and approves SAS programming instructions and CDISC/ADaM specifications.
Performs statistical analysis and simulations using SAS to support clinical trial design and data interpretation.
Reviews and provides input on eCRF design, external vendor data specifications, edit checks, and other Data Management related documents to ensure appropriate data collection for statistical programming.
Works closely with biostatisticians and data managers to identify data issues and generate queries that may impact statistical analysis and/or programming.
Works closely with biostatisticians and other functions (Pharmacovigilance, Clinical Development, etc.) to support data review for internal stakeholders.
Assists with ensuring consistency across programming methods in similar studies within a program.
Requirements
Bachelor's degree or master's degree or higher in statistics, biostatistics, or other closely related discipline with a minimum of 8 years of relevant experience in the pharmaceutical/biotechnology industry.
Experience in applying clinical trial and statistical methodology to a variety of studies and indications across various phases of clinical development.
Knowledge of pharmaceutical and regulatory requirements, procedures, and policies.
Experience With BLA Or NDA/sNDA Submissions Is Required.
Knowledge of GCP, ICH, 21 CFR part 11, and other Guidance documents and policies related to clinical trials operations requirements.
In depth knowledge of CDISC and ADaM data set structures and requirements.
Proficiency with SAS programming skills to including knowledge of SAS ODS graphical procedures such as PROC SGPLOT and the graphics template language (GTL) Knowledge of all aspects of clinical drug development (Phase 1-4).
Experience working with a CRO partner.
Excellent computer skills; strong verbal and written communication skills
Ability to work well in a team environment as a contributor.
