Senior Regulatory Submissions Lead - Hybrid

AbbVie; Florham Park (NJ); Híbrido; USD 85 000 - 162 000; Tempo integral

Resumo da oferta

AbbVie, a global biopharmaceutical company, seeks a Senior Associate Regulatory Affairs Submission Management for a hybrid schedule in Florham Park, NJ. You will manage medium to high impact regulatory submissions, coordinate publishing activities, and partner with cross‑functional teams to ensure timely, compliant dossiers.

The role requires 4+ years in regulatory affairs or related fields with publishing software proficiency; PMP and RAC credentials are a plus, and a Bachelor's degree is

Qualificações

• Required Education: Bachelor's degree.
• Note: Years of experience may also compensate for lower education.
• Preferred Education: PMP and RAC certificates a plus
• Required Experience: 4 years' pharmaceutical or industry related experience with publishing related software tools e.g. Documentum, eCTDXPress/ISIPublisher, ISI Toolbox/DocuBridge/Insight platform, Adobe Acrobat.
• Preferred Experience: Experience in Regulatory Affairs preferred but may consider QA, R&D/support, Scientific affairs, operations or related area
• Experience in Regulatory Operations, including regulatory submission project management and/or submission publishing is preferred.
• Proven leadership skills and presence
• NOTE: Higher education may compensate for years of experience.

Responsabilidades

• Manages medium to high impact submission projects to ensure the timely delivery of high-quality dossiers that meet technical specifications defined by regulatory authorities and can be easily navigated and reviewed by a regulatory agency.
• Acts as RA Submissions interface with project teams providing guidance and communication of established submission processes and standards. Provides input to project scope, especially as it impacts publishing timelines and deliverables.
• Plans and conducts submission team meetings. Expedites, manages, and coordinates multiple concurrent interrelated activities for submission projects and/or for multiple products in the delivery of moderately complex published submissions within the required timelines. Anticipates obstacles and develop solutions within the team.
• Coordinates submission publishing with offsite publishers/provides notification to ensure all required resources are available to meet submission timelines. Prepares content planner for publishing and works with vendor to resolve publishing issues. May perform in-house publishing tasks
• May be a technical Subject Matter Expert troubleshooting issues and providing technical systems support.
• Facilitates the creation or procurement of submission content deliverables such as cover letters and forms.
• Performs detailed quality reviews of published output to ensure compliance with Regulatory Standards and Health Authority guidances including verification of content, bookmarks, hypertext links and tables of content in moderately complex submissions. Facilitates team reviews.
• Suggests and contributes to process improvements, including changes to software and business processes. May participate on internal project teams to update business software.
• Demonstrates team leadership skills and ability to influence without direct authority. Builds and maintains positive relationships internally and externally.
• Contributes to the development of optimal business processes and standards within the department to ensure high levels of customer support and to achieve high quality submissions.
• Contributes to the creation, and implementation of internal process and standards documents relating to publishing and publishing deliverables.

Conhecimentos

Regulatory submissions

Leadership

Cross-functional collaboration

Publishing software

Formação académica

Bachelor's degree

PMP certification

RAC certification

Ferramentas

Documentum

ISIPublisher / eCTDXPress

ISI Toolbox

DocuBridge / Insight

Adobe Acrobat

Descrição da oferta de emprego

AbbVie, a global biopharmaceutical company, seeks a Senior Associate Regulatory Affairs Submission Management for a hybrid schedule in Florham Park, NJ. You will manage medium to high impact regulatory submissions, coordinate publishing activities, and partner with cross‑functional teams to ensure timely, compliant dossiers.

The role requires 4+ years in regulatory affairs or related fields with publishing software proficiency; PMP and RAC credentials are a plus, and a Bachelor's degree is