Provides statistical input into protocol and case report form (CRF) development in all therapeutic areas (e.g., trial design, sample size estimation, randomization, statistical methods for protocols, edit checks for clinical trial data). Communicates with clients regarding study protocol or statistical analysis issues. Writes detailed statistical analysis plans including specifications for analysis files, consistency checks, tables, and figures. Analyzes clinical trial data producing accurate results representing the outcome of the trial. Validates statistical output. Accurately interprets statistical results and concepts. With the medical writer, co-authors final integrated reports of clinical trial data by writing thorough and clear statistical methods sections and producing the statistical appendix for the final report. Provides input into statistical standard operating procedures (SOPs) and general standardization efforts within the department (e.g., statistical methodology standards, standard data presentations). Participates in interactions with regulatory agencies, as required. Collaborates effectively with members of clinical trial implementation teams and with Biometrics colleagues.

Provided statistical input into protocol and case report form (CRF) development in all therapeutic areas (e.g., trial design, sample size estimation, randomization, statistical methods for protocols, edit checks for clinical trial data). Communicated with clients regarding study protocol or statistical analysis issues. Wrote detailed statistical analysis plans including specifications for analysis files, consistency checks, tables, and figures. Analyzed clinical trial data producing accurate results representing the outcome of the trial. Validated statistical output. Accurately interpreted statistical results and concepts. With the medical writer, co-authored final integrated reports of clinical trial data by writing thorough and clear statistical methods sections and producing the statistical appendix for the final report. Provided input into statistical standard operating procedures (SOPs) and general standardization efforts within the department (e.g., statistical methodology standards, standard data presentations). Participated in interactions with regulatory agencies, as required. Collaborated effectively with members of clinical trial implementation teams and with Biometrics colleagues.

Assisted in the development of documents produced by the Biostatistics department including statistical analysis plans, other statistical reports and documents utilized by corporate compliance (SOPs, reference tools, standard forms). Drafted statistical table, listing, and figure shells. Assisted Biometrics colleagues in the development of analysis dataset specifications. Assisted in the review of analysis datasets using SAS Viewer. Assisted in the development of Randomization Plans. Performed patient randomization assignments. Produced and validated simple tables, listings, and figures. Reviewed statistical output for consistency, formatting, grammar, etc. Provided input into statistical Standard Operating Procedures (SOPs) and general standardization efforts within the department. Collaborated effectively with members of clinical trial implementation teams and with Biometrics colleagues. Attended project team meetings as required. Initiated, organized, and participated in statistical initiatives and any management requested activities. Compiled statistical data packages. Developed and maintained an on-line library of statistical journal articles. Drafted SDTM and ADaM reviewers guides and define.pdfs.

Performed tasks related to the design and conduct of clinical studies and the analyses of clinical trial data. Assisted in the development of documents produced by the Biostatistics department including statistical analysis plans, other statistical reports and documents utilized by corporate compliance (SOPs, reference tools, standard forms). Drafted statistical table, listing, and figure shells. Assisted Biometrics colleagues in the development of analysis dataset specifications. Assisted in the review of analysis datasets using SAS Viewer. Assisted in the development of Randomization Plans. Performed patient randomization assignments. Produced and validated simple tables, listings, and figures. Reviewed statistical output for consistency, formatting, grammar, etc. Provided input into statistical Standard Operating Procedures (SOPs) and general standardization efforts within the department. Collaborated effectively with members of clinical trial implementation teams and with Biometrics colleagues. Attended project team meetings as required. Initiated, organized, and participated in statistical initiatives and any management requested activities. Compiled statistical data packages. Developed and maintained an on-line library of statistical journal articles.

Worked with a team of students to design and publish an R software package to process and manipulate wood product carbon accounting data for use by the US Forest ServiceModeled various uncertainties and sensitivities to input in calculating wood product carbon sequestrationPresented package and research findings at 2017 NACP Principal Investigators meetingWriting paper on project for publicationProject summary and R package install: http://alanarnholt.github.io/WOODCARB3R/Project code: https://github.com/alanarnholt/USFS