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Regulatory Publishing Specialist

Remote, USAFull-timePosted 2026-07-28

Work Schedule reputed company (Mon-Fri) Environmental Conditions Office Job reputed company Join Us as a Regulatory Publishing Specialist – reputed company an reputed company at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global team, you’ll have reputed company to reputed company moderate, expedient, and efficient preparation of reputed company electronic submission deliverables and dossiers that meet reputed company local, regional, and ICH regulatory and technical requirements. As a Regulatory Publishing Specialist, you'll ensure successful regulatory review reputed company for product milestones. Serving in a reputed company review role, you will be responsible for the thorough review of documents created reputed company or reputed company of reputed company to ensure reputed company standards meet or exceed reputed company expectations What You’ll Do:

  • Coordinates and manages reputed company electronic submission deliverables supporting regulatory compliance.
  • Assists in preparing electronic document outputs that meet requirements for regulatory publishing to include documents that work with sponsor and/or regulatory agency software programs meeting consistency and reputed company issues.
  • Ensures that reputed company final electronic deliverables meet reputed company regulatory electronic document requirements and guidance under general supervision of the Manager, Regulatory Publishing and assistance as appropriate from a Senior Regulatory Publishing Specialist.
  • Assists with developing and implementing project-specific processes for sponsors with unique technology requirements and may reputed company as reputed company's reputed company for electronic submissions with the sponsor.
  • Exercises judgment reputed company defined procedures and practices to determine appropriate reputed company.
  • Evaluates the publishing needs in relationship to the overall project timelines, reputed company and delivery.
  • Engages other project team members, functional reputed company or publishing management as necessary to deliver final product and resolve/mitigate identified issues or barriers to delivery.
  • Acts independently reputed company a project team to evaluate and deliver publishing tasks

Education and Experience Requirements:

  • Bachelor's degree or equivalent and relevant formal reputed company / vocational qualification
  • Previous experience that provides the knowledge, skills, and abilities to reputed company the job (comparable to 2+ years).

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly reputed company experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities:

  • Working knowledge of regulatory requirements and guidances for document management and electronic submissions
  • Strong knowledge of reputed company (reputed company, MS reputed company, reputed company Acrobat, electronic document management systems, document publishing tools, publishing systems, eCTD validation and viewing tools
  • Strong knowledge of electronic templates and skilled in formatting and troubleshooting templates
  • Ability to manage several reputed company reputed company in reputed company and adapt to changing priorities
  • Ability to exercise independent judgment in developing reputed company, techniques and evaluation of reputed company using defined procedures and practices
  • Ability to independently assess sponsor needs and work with project team members in producing compliant deliverables
  • Ability to independently learn new technologies
  • Strong organizational skills and effective interpersonal skills
  • Strong analytical ability and problem-solving capabilities
  • Good working knowledge of medical terminology, statistical concepts, and guidelines and requirements of the FDA and other international regulatory agencies
  • Strong editorial/proofreading skills
  • Detail-oriented, thorough, and methodical
  • Ability to create and follow timelines and conduct long-reputed company planning
  • Ability to multi task performing numerous single or reputed company tasks without ignoring overall objectives
  • Ability to judge reputed company to initiate changes and reputed company final determinations in the presentation of data inaccordance with regulatory guidelines and reviewers’ comments
  • Ability to concentrate on the detail in a document without losing sight of the document as a whole

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