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Goldbelt, Inc.

Biostatistician

Goldbelt, Inc.

ApplySave Job
  • Date Posted

    Today

    New!
  • Remote Work Level

    No Remote

  • Location

    Silver Spring, MD

  • Job Schedule

    Part-Time

  • Salary

    $50 HOURLY

  • Benefits

    Professional/Career Development 401k Matching/Retirement Savings Dental Insurance Health/Medical Insurance Vision Insurance Paid Vacation

  • Categories

    Consulting,  Government,  Data Science,  Healthcare,  Research

  • Job Type

    Freelance,Temporary

  • Career Level

    Experienced

  • Travel Required

    No Specification

  • Education Level

    Master's Degree

About the Role

Title: Biostatistician

Location: Maryland, United States

Healthcare

Goldbelt Apex, LLC

Public Trust

19655

RFP

Overview

Please note that this position is contingent upon the successful award of a contract currently under bid.

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.

This is a part-time consulting opportunity anticipated to run for approximately 10 months.
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:

  • Part-Time Consultant
  • Approximately 10-Month Period of Performance

Pay and Benefits

Pay for this position is $50.00 hourly.

At Goldbelt, we value and reward our team's dedication and hard work. We provide a competitive base salary commensurate with your qualifications and experience. As an employee, you'll enjoy a comprehensive benefits package, including medical, dental, and vision insurance, a 401(k) plan with company matching, tax-deferred savings options, supplementary benefits, paid time off, and professional development opportunities.

Apply

FAQs About Biostatistician Jobs at Goldbelt, Inc.

This job offers No Remote Work.
Part-Time
Yes, the benefits include Professional/Career Development, 401k Matching/Retirement Savings, Dental Insurance, Health/Medical Insurance, Vision Insurance and Paid Vacation.
$50 HOURLY
Consulting, Government, Data Science, Healthcare, Research
You can apply directly using the apply button given on the page.
Residents of Silver Spring, MD or United States
The work location for this position will be Silver Spring, MD
Experienced
The required education level for this role is Master's Degree

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