Manager - Regulatory Affairs Submission Systems and Support (Hybrid)

Company: AbbVie
Location: Florham Park
Posted on: April 5, 2026

Job Description:

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description The Manager, Regulatory Affairs Submission Management is responsible for providing expert support and continuous improvement for all publishing systems used by the RA Submission Management team. Responsible for providing functional leadership in system upgrades, process enhancements, and large scale platform initiatives, while also fostering collaboration across global Submission Management teams. This role is responsible for ensuring robust and efficient operations, driving innovation, and advocating for timely delivery of technology solutions. Responsibilities Serve as the primary point of contact and subject matter expert for publishing related systems, providing day-to-day support and guidance. Partner with BTS to lead and execute system upgrades from the business perspective, including impact analysis, user acceptance testing, job aid updates, training and communication, and installation confirmation. Lead, develop, and maintain tools and templates for the Submission Management team. Possess a working knowledge of submission management business processes and associated regulations and using the knowledge, collaborate with global teams to enhance publishing processes and implement solutions. Prepares and delivers effective management communication that efficiently frames complex issues and leads to actionable decisions. Develop and deliver training documentation and provide end user training for new systems and processes. Actively drive and implement new ideas to enhance the effectiveness, quality, and efficiency of the Submission Management team. Foster open, constructive communication with stakeholders, transparently resolving conflict and leveraging feedback for improvement. Qualifications Minimum Qualifications Bachelors degree (note: Higher education may compensate for years of experience. Years of experience may also compensate for lower education.) 6 years of pharmaceutical or industry related experience with RIM and publishing related software tools (e.g. Documentum, Generis CARA, docuBridge, Toolbox) 1-2 years in cross functional project management Preferred Qualifications: PMP and RAC certificates a plus Sharepoint related coursework/certifications Power Apps/Power Automate experience Power BI experience Other Required Skills: Strong communication skills, both oral and written Strong analytical skills and attention to detail Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law: The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemay ultimatelypay more or less than the posted range. This range may be modified in thefuture. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees. This job is eligible to participate in our short-term incentiveprograms. Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employee remains in the Company's sole andabsolutediscretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent withapplicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Keywords: AbbVie, Stratford , Manager - Regulatory Affairs Submission Systems and Support (Hybrid), IT / Software / Systems , Florham Park, Connecticut