Regulatory Affairs Associate Job at Stark Pharma Solutions Inc, New Jersey

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  • Stark Pharma Solutions Inc
  • New Jersey

Job Description

Job Title: Regulatory Affairs Associate

Location: Florham Park, NJ (Hybrid)

Experience: 5+ Years
Duration: 12+ months contract
Eligibility: US Citizens or Green Card holders only

Job Summary

The Regulatory Affairs Associate / Regulatory Publisher will support U.S. regulatory submissions and publishing activities within a pharmaceutical environment. This role focuses on eCTD publishing, promotional material submissions, and regulatory documentation management while ensuring compliance with FDA regulations and internal standards.

Key Responsibilities
  • Support preparation, publishing, and submission of U.S. regulatory filings in eCTD format

  • Perform eCTD lifecycle management including publishing, validation, and quality checks

  • Manage AdPromo and PromoMats submissions in compliance with FDA requirements

  • Compile, format, and publish regulatory documents using approved tools and templates

  • Ensure accuracy, completeness, and timeliness of regulatory submissions

  • Coordinate with Regulatory Affairs, Labeling, and cross-functional teams to meet submission timelines

  • Maintain submission archives and regulatory documentation in electronic systems

  • Troubleshoot publishing issues and resolve technical errors related to eCTD submissions

  • Follow FDA guidelines, SOPs, and regulatory standards for submission readiness

Required Qualifications
  • Bachelor's degree in Life Sciences, Pharmacy, or a related field

  • 0 3 years of experience in Regulatory Affairs or Regulatory Publishing within the pharmaceutical industry

  • Hands-on experience with eCTD publishing and submissions

  • Experience with AdPromo and promotional material submissions

  • Working knowledge of FDA regulations and submission processes

  • Proficiency with regulatory publishing tools such as DocuBridge and eCTDXpress

  • Strong attention to detail and document management skills

  • Ability to work in a hybrid onsite/remote environment

  • Strong communication and coordination skills

Preferred Skills
  • Prior experience supporting U.S. FDA submissions

  • Familiarity with regulatory document lifecycle management

  • Ability to manage multiple submissions and deadlines simultaneously

Job Tags

Contract work, Remote work,

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