A Biostatistician conducts statistical analysis of health and biology-related data. Analysis may be used for product development at a pharmaceutical company, disease research at a hospital or health policy research at a public health organization.
Biostatistician Goldbelt, Inc. - 3.0 Silver Spring, MD Job Details Part-time $50 an hour 11 hours ago Qualifications Project reporting Statistics Data preprocessing Content creation for technical audiences Statistics Biostatistics-based research Medical statistical report preparation Data validation techniques XML Technical documentation Data quality assurance Data quality monitoring Quality control Clinical program data analysis CDISC standards Regulatory submission editing and review Clinical research documentation Technical writing experience within technology Clinical research reports Cross-functional collaboration Clinical data analysis Project stakeholder communication Cross-functional communication Progress tracking (project management tasks) Scientific reports
Full Job Description Overview:
Goldbelt Apex, a part of the Healthcare Technology Transformation Group, is a data-focused company dedicated to process and quality in every aspect. As experts in healthcare IT experts, Apex is committed to building systems for healthcare organizations to seamlessly communicate and exchange data across different systems and devices.
Summary:
We are seeking a qualified Biostatistician to provide statistical and clinical trial support for a Phase II clinical research effort supporting the Walter Reed Army Institute of Research (WRAIR). The selected candidate will support regulatory-focused statistical analysis activities, including CDISC-aligned deliverables and study closeout support associated with FDA submission requirements.
Responsibilities:
Essential Job Functions:
Perform statistical analyses in accordance with approved Statistical Analysis Plans (SAPs) Support development, review, and validation of CDISC-compliant deliverables, including: SDTM datasets ADaM datasets Define.xml documentation
SDRG/ADRG
documentation Generate and validate Tables, Listings, and Figures (TLFs) Conduct data cleaning, quality control, and statistical validation activities Support clinical study closeout and regulatory submission activities Coordinate with clinical research and project teams to support data review and analysis workflows Prepare technical documentation and contribute to study reports and presentations Participate in project status meetings and provide progress updates
Qualifications:
Necessary Skills and Knowledge:
Perform statistical analyses in accordance with approved Statistical Analysis Plans (SAPs) Support development, review, and validation of CDISC-compliant deliverables, including: SDTM datasets ADaM datasets Define.xml documentation
SDRG/ADRG
documentation Generate and validate Tables, Listings, and Figures (TLFs) Conduct data cleaning, quality control, and statistical validation activities Support clinical study closeout and regulatory submission activities Coordinate with clinical research and project teams to support data review and analysis workflows Prepare technical documentation and contribute to study reports and presentations Participate in project status meetings and provide progress updates
Minimum Qualifications:
Master's degree or higher in Biostatistics, Epidemiology, Statistics, Public Health, or related field Experience supporting clinical research or clinical trial studies Experience developing or executing Statistical Analysis Plans (SAPs) Experience with statistical programming and analysis using SAS, R, STATA, or similar tools Experience generating statistical outputs including Tables, Listings, and Figures (TLFs) Strong understanding of data validation, quality control, and analytical workflows Ability to work independently and collaboratively in cross-functional scientific environments Strong written and verbal communication skills Able to to successfully complete a background investigation and satisfy Government access requirements prior to beginning work.
Preferred Qualifications:
Experience supporting FDA-regulated clinical trials Hands-on experience with CDISC standards, including SDTM and ADaM Experience preparing Define.xml, SDRG, and ADRG documentation Experience supporting regulatory submission packages Prior experience supporting Department of Defense (DoD), federal health, or military research organizations Familiarity with clinical data structures, including demographics, adverse events, laboratory, and longitudinal outcomes data
Work Location:
Primary support is associated with WRAIR in Silver Spring, MD. Remote work may be permitted, subject to task requirements and Government approval.
Position Type:
Approximately 10-Month Period of Performance Pay and Benefits Pay for this position is $50.00 hourly.
