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Regulatory Biostatistician
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FileImport - Laulima Government Solutions
Frederick, MD (In Person)
Full-Time
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Job Description
Regulatory Biostatistician
Bering-Alaka`ina Holdings (BAH) has a need for a Regulatory Biostatistician to support our government customer located in Frederick, Maryland.
Prepare and coordinate the development of analysis plans, table specifications and shells, write and perform programming of specifications for analysis files, consistency checks, tables, listings and figures.
Perform data review and statistical analyses using SAS software.
Communicate with clients regarding study protocol or statistical analysis issues as they arise, provide expert statistical advice on statistical deliverables, and shall communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results.
Interpret analyses and write statistical sections of study reports, including integrated reports. Have strong written and verbal communication skills to be able to present and discuss experimental results at group/project team meetings and scientific conferences.
Be able to work independently based on broad guidelines and objectives provided by the government point of contact as well as be able to work in a team structure and interface with different research and development departments.
Collaborate with study directors, PIs, and other key staff to perform statistical analyses and provide statistical support for approximately 30 clinical and approximately 100 nonclinical protocols annually, and comply with the FDA GLP and GCP regulations, when applicable.
Develop biostatistical aspects of study designs, statistical analysis plans, statistical analyses, study reports, and other relevant documents and efforts. Provide consultative support on the statistical suitability and regulatory compliance of
DESCRIPTION OF RESPONSIBILITIES
Biostatistics provides biostatistical support to all research elements within USAMRIID, including clinical and non-clinical research projects. Biostatisticians work closely with study directors, Principal Investigators (PIs), and other key staff to design and perform statistical analyses, and product development strategies from the perspective of applicable FDA and animal care and use guidelines.REQUIRED DEGREE/EDUCATION/CERTIFICATION
MS in biostatistics, with eight (8) years of experience in performing clinical or pre-clinical statistical analysis. (As a substitute for the MS in biostatistics, a related MS degree with substantial (30+ hours) of statistics coursework would be acceptable.) Examples of alternate majors which, combined with a concentration in statistics, would fulfill this requirement include Mathematics, Operations Research, Epidemiology, Public Health, or Behavioral Health and Sciences.REQUIRED SKILLS AND EXPERIENCE
Provide FDA regulatory biostatistical support to USAMRIID's science and technology and medical countermeasure test and evaluation capabilities to facilitate approval of biomedical products by FDA.Develop statistical methods sections of study plans and protocols, including sample size calculations, and shall review study case report forms for advanced clinical and non-clinical studies to be conducted in compliance with FDA's Good Laboratory Practice (GLP) regulation, Good Clinical Practice (GCP) regulation, and relevant sections of other FDA regulations, e.g., 21 CFR Part 58 and 21 CFR Part 11.Advise data management staff on database design, validation checks, and critical data during the clinicalonclinical database development process.Prepare and coordinate the development of analysis plans, table specifications and shells, write and perform programming of specifications for analysis files, consistency checks, tables, listings and figures.
Perform data review and statistical analyses using SAS software.
Communicate with clients regarding study protocol or statistical analysis issues as they arise, provide expert statistical advice on statistical deliverables, and shall communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results.
Interpret analyses and write statistical sections of study reports, including integrated reports. Have strong written and verbal communication skills to be able to present and discuss experimental results at group/project team meetings and scientific conferences.
Be able to work independently based on broad guidelines and objectives provided by the government point of contact as well as be able to work in a team structure and interface with different research and development departments.
Collaborate with study directors, PIs, and other key staff to perform statistical analyses and provide statistical support for approximately 30 clinical and approximately 100 nonclinical protocols annually, and comply with the FDA GLP and GCP regulations, when applicable.
Develop biostatistical aspects of study designs, statistical analysis plans, statistical analyses, study reports, and other relevant documents and efforts. Provide consultative support on the statistical suitability and regulatory compliance of