Compunnel
Proofreader
Compunnel, Richmond, Virginia, United States, 23214
Job Description :The Regulatory Document Proofreader will support the preparation and submission of FDA regulatory applications for tobacco-related projects. This role demands exceptional attention to detail, expertise in scientific document formatting, and a strong command of tools such as Starting Point, EndNote, and SharePoint. The ideal candidate will have prior experience in regulatory work within the tobacco or pharmaceutical industries, focusing on ensuring narrative consistency and adherence to style guidelines.Responsibilities :
Proofreading and Editing:Review regulatory application sections for narrative consistency and clarity.Ensure proper grammar, punctuation, and conformance to ALCS style guides.
Formatting and Conversion:Apply electronic software formatting to regulatory application sections.Convert reference articles into publishable formats adhering to journal submission standards.
Compliance and Quality Assurance:Ensure documents meet FDA regulatory requirements and scientific publishing standards.Cross-check references and ensure consistency across all sections of applications.
Training and Guidance:Provide input and best practices on formatting science documents for journal submissions.
Requirements :
Technical Expertise:Proficient in Starting Point, EndNote, and SharePoint.
Industry Experience:At least 5+ years of relevant experience in regulatory document proofreading or scientific writing.Previous exposure to FDA regulatory work in the tobacco or pharmaceutical industries is highly preferred.
Skills:Exceptional attention to detail with strong proofreading skills.Ability to work independently while meeting tight deadlines.Familiarity with scientific manuscript preparation and journal submission standards.
Work Hours:20 hours per week, with potential for increased hours based on departmental needs.
Ideal Candidate Traits :
Strong organizational and multitasking abilities to handle multiple document revisions.Ability to adapt to evolving regulatory standards and project priorities.Excellent communication and collaboration skills to work with cross-functional teams.
Location
Center for Research & Technology
Center for Research & Technology-601 E Jackson St
Proofreading and Editing:Review regulatory application sections for narrative consistency and clarity.Ensure proper grammar, punctuation, and conformance to ALCS style guides.
Formatting and Conversion:Apply electronic software formatting to regulatory application sections.Convert reference articles into publishable formats adhering to journal submission standards.
Compliance and Quality Assurance:Ensure documents meet FDA regulatory requirements and scientific publishing standards.Cross-check references and ensure consistency across all sections of applications.
Training and Guidance:Provide input and best practices on formatting science documents for journal submissions.
Requirements :
Technical Expertise:Proficient in Starting Point, EndNote, and SharePoint.
Industry Experience:At least 5+ years of relevant experience in regulatory document proofreading or scientific writing.Previous exposure to FDA regulatory work in the tobacco or pharmaceutical industries is highly preferred.
Skills:Exceptional attention to detail with strong proofreading skills.Ability to work independently while meeting tight deadlines.Familiarity with scientific manuscript preparation and journal submission standards.
Work Hours:20 hours per week, with potential for increased hours based on departmental needs.
Ideal Candidate Traits :
Strong organizational and multitasking abilities to handle multiple document revisions.Ability to adapt to evolving regulatory standards and project priorities.Excellent communication and collaboration skills to work with cross-functional teams.
Location
Center for Research & Technology
Center for Research & Technology-601 E Jackson St