Junior Programmer at Professional Stewards Services PSS LLC
Washington, District of Columbia, USA -
Full Time


Start Date

Immediate

Expiry Date

17 Oct, 25

Salary

90000.0

Posted On

18 Jul, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Platforms, Databases, Responsive Web Design, Interoperability, Web Api, Regulatory Policy, Html, Css, Sql, Jquery

Industry

Information Technology/IT

Description

PROFESSIONAL STEWARDS SERVICES IS SEEKING AN ENERGETIC, SELF-STARTER TO JOIN OUR GROWING TEAM TO SUPPORT OUR PROGRAMMING UNIT.

Work location: Silver Spring, MD/Washington DC (Hybrid)
Salary: up to $90,000
Hours: Full time
Education Requirements: Bachelor’s Degree

REQUIRED SKILLS AND QUALIFICATIONS:

  • Must be a U.S. Citizen.
  • Must be able to obtain a security clearance.
  • 3-5 years of experience
  • Familiarity with FDA’s CDER’s new drug review process
  • Strong analytical and problem-solving skills.

PREFERRED QUALIFICATIONS:

  • Experience working with the FDA.
  • Ability to work productively from home.
    Skills: C#, VB, ASP.NET Web Forms, SQL Database, HTML, CSS, Java Script, Responsive Web Design, Web API or SOA Experience, SQL, Entity Framework Bootstrap, JQuery

Job responsibilities include:

  • System Enhancements: Modify database architecture, IT platforms, data fields, tables, reporting functionalities, and user interfaces.
  • Interoperability: Ensure system integrates effectively with other FDA IT tools, platforms, and databases.
  • Process Updates: Adapt procedures and data collection methods in response to changes in science, regulatory policy, or to maintain consistency with other FDA informatics efforts.

How To Apply:

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Responsibilities
  • System Enhancements: Modify database architecture, IT platforms, data fields, tables, reporting functionalities, and user interfaces.
  • Interoperability: Ensure system integrates effectively with other FDA IT tools, platforms, and databases.
  • Process Updates: Adapt procedures and data collection methods in response to changes in science, regulatory policy, or to maintain consistency with other FDA informatics efforts
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