Senior Regulatory Submissions Associate — Hybrid 3/2

AbbVie; Illinois; Hybrid; USD 90,000 - 135,000; Full time

Job summary

AbbVie seeks a Senior Associate in Regulatory Affairs Submission Management to oversee medium to high impact submission projects, coordinating with cross-functional teams and publishing vendors to meet timelines and regulatory standards.

The role supports development, marketing, and post-marketing filings, with a hybrid schedule at AbbVie locations in NJ or IL. Strong communication and leadership are key requirements.

Qualifications

• Bachelor's degree required; years of experience may compensate.

Responsibilities

• Manages medium to high impact regulatory submission projects to ensure timely delivery of high quality dossiers.

Skills

Team leadership

Influence without authority

Mentoring

Education

Bachelor's degree

Tools

Documentum

eCTDXPress/ISIPublisher

ISI Toolbox/DocuBridge/Insight

Adobe Acrobat

Job description

AbbVie seeks a Senior Associate in Regulatory Affairs Submission Management to oversee medium to high impact submission projects, coordinating with cross-functional teams and publishing vendors to meet timelines and regulatory standards.

The role supports development, marketing, and post-marketing filings, with a hybrid schedule at AbbVie locations in NJ or IL. Strong communication and leadership are key requirements.