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Junior Analyst

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Onsite

Junior Analyst

SMX Services & Consulting, Inc.

Junior Analyst

Skills

Testing & QA

2 months ago

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Important information


Contract type:

Other

Location:

Rockville, MD, USA

Work mode:

Onsite

Published on:

8 August 2026

What they need


Junior Analyst - FDA DASH Regulatory Data / Database Curation

U.S. CITIZENS ONLY

Client:  U.S. Food and Drug Administration (FDA) - CDER

Location:  Primarily Remote - occasional onsite work in Silver Spring, MD / Washington, DC area

Duration:  12 Months - contingent upon contract award

Pay Rate:   $44.27-$46.15/hour

Start Date:  Upon contract award and completion of FDA security requirements

Position Summary

SMX Services & Consulting is seeking a  Junior Analyst  to support the FDA’s  DASH Knowledge Management program .

The position focuses on reviewing FDA and pharmaceutical regulatory documents, extracting important information, entering and maintaining data in the DASH database, and ensuring data is  accurate, complete, and consistent .

Key Responsibilities

  • Review FDA and pharmaceutical regulatory documents.
  • Extract and enter regulatory and scientific data into the DASH database.
  • Standardize and validate data according to FDA procedures.
  • Perform data quality and QA/QC reviews.
  • Use Excel and database applications to manage and verify information.
  • Identify missing, inconsistent, or questionable data and escalate issues when needed.
  • Follow DASH procedures, SOPs, data definitions, and business rules.
  • Maintain database and project documentation.
  • Assist with updates to SOPs, user guides, and data definitions.
  • Work with FDA subject-matter experts, technical teams, and contractors.
  • Protect confidential and sensitive FDA information.

Required Qualifications

  • U.S. Citizen
  • Bachelor’s degree (BA or BS).
  • 2+ years of professional experience.
  • Experience with  data analysis and data standardization .
  • Experience with  Microsoft Excel and/or database software .
  • Strong attention to detail and data accuracy.
  • Ability to review and interpret technical or scientific information.
  • Ability to follow established procedures and data standards.
  • Must be able to meet FDA security requirements.

Preferred Experience

Candidates with any of the following experience are strongly preferred:

  • FDA or other government experience.
  • FDA  CDER new drug review process .
  • Regulatory or pharmaceutical documentation.
  • IND, NDA, BLA, or efficacy supplement  documentation.
  • Pharmaceutical, biomedical, clinical trial, or regulatory science experience.
  • Life sciences or statistical background.
  • Regulatory data collection, analysis, or quality assurance.
  • Experience with FDA systems.

Highly Preferred

Previous FDA DASH experience , particularly with:

  • DASH database data entry and curation.
  • DASH QA/QC procedures.
  • DASH SOPs and data standards.
  • Regulatory document review.

Security Requirements

Candidates must be able to complete  NACI and Level 5 Public Trust processing , fingerprinting, FDA security/privacy training, and required confidentiality agreements.

Pay Rate: $44.27-$46.15/hour

Important:  This position is contingent upon  SMX receiving the contract award and FDA approval of the proposed candidate .

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