Jobs at AbbVie

Lead global regulatory strategy and the Global Regulatory Product Team for assigned therapeutic products. Develop and implement regulatory dossiers, labeling strategies, and mitigation plans across development and lifecycle; interface with cross-functional and senior leadership; ensure global compliance; mentor team members and represent AbbVie's regulatory positions.

Lead design and execution of patient experience data and clinical outcome assessment (COA) research for oncology; manage cross-functional partnerships, global regulatory and payer interactions, validate patient-reported measures, oversee multi-product strategies, mentor junior staff, manage vendors and budgets, and publish and present findings to support registration, access, and clinical practice.

Lead strategy, governance, and operations for a new Practice Economics function: set priorities, run operating cadence, lead cross-functional initiatives, create executive communications, and build performance dashboards to drive disciplined execution and stakeholder alignment.

Lead strategy, operations, and governance for Practice Economics. Drive strategic planning, cross-functional initiative execution, operating rhythms, performance management, executive communications, and stakeholder alignment to scale a new function and deliver measurable business and customer impact.

Lead CMC regulatory strategy and submissions (INDs/CTAs, marketing applications, amendments). Advise cross-functional teams, liaise with health authorities, manage change control, develop policies, and mentor staff to enable first-pass approvals.

Lead and develop a data standards team to create, govern, and maintain end-to-end clinical data standards (CDASH, SDTM, ADaM, define.xml). Oversee eCRF design review, SDTM conformance mapping, metadata repository governance, regulatory submission readiness, training, cross-functional communication, and CDISC community engagement.

Lead 340B strategy and operations within AbbVies Center of Excellence: monitor external landscape, develop investigative and audit-ready processes, support audits and disputes, create analytics and training, inform advocacy and policy, and collaborate cross-functionally to drive compliance, mitigation, and strategic solutions for 340B program impacts.

Lead and own integrated asset strategy from discovery through lifecycle for aesthetics assets. Chair Asset Strategy Team, align cross-functional plans (development, regulatory, commercial, manufacturing), advise governance and senior leadership, define Go/No-Go decision points, and drive resource, budget, and competitive strategy while mentoring teams and representing the asset externally.

Responsible for GMP batch documentation review and clinical supply disposition for NBE/NCE/ATMP programs. Provides QA oversight of TPMs and AbbVie sites, leads deviations/investigations, authors quality documents, oversees supplier qualification and quality agreements, monitors PDQA metrics, supports inspection readiness, mentors junior staff, and drives continuous improvement to ensure compliant, timely clinical supply.

Leads clinical development programs, ensuring compliance and effective execution of clinical trials while managing teams and project timelines.

The Copy Supervisor leads copy development for various media in pharmaceutical advertising, manages workloads, and collaborates with teams to meet client needs while mentoring copywriters.

The Head of Global Fillers and Regenerative Injectables is responsible for the strategy and management of Allergan Aesthetics' product pipeline, leading teams, ensuring collaboration among functions, and driving product commercialization and innovation.

Partnering with the franchise VP, leads project management and internal communications for the Eye Care franchise. Manages scope, plans, logistics, calendars, and cross-functional initiatives (town halls, national meetings, executive presentations). Designs and executes communications strategy and employee engagement channels, measures impact with analytics, and ensures alignment between commercial, sales, and IBT stakeholders to drive awareness, adoption, and change management.

Lead US OTC Consumer Eye Care franchise strategy, P&L, and portfolio growth. Own brand architecture, omnichannel marketing, launches, commercialization, and cross-functional enterprise planning. Drive revenue, market share, margin delivery, and build a high-performing, matrixed team while partnering with Sales, R&D, Supply Chain, Finance, and Medical/Regulatory.

Lead US & Canada regulatory strategy and lifecycle activities for aesthetics medical devices. Manage FDA interactions, prepare regulatory submissions and briefing packages, support cross‑functional stakeholders, and ensure compliance with regional requirements and post‑approval obligations.

Advise cross-functional R&D and business teams on patent strategy for pharmaceutical products (focus neuroscience). Draft, file, and prosecute worldwide patent applications; manage outside counsel; defend and challenge patents in post-grant proceedings; perform prior art searches, third-party patent analysis, and due diligence to support business development.

Field-based scientific expert supporting Hematology/Oncology medical objectives. Develops and executes territory and HCP/investigator engagement plans, delivers scientific education, documents data point observations, supports clinical development and research initiatives, and collaborates with cross-functional field teams to meet territory goals while ensuring regulatory and company policy compliance.

Provide onsite administrative support to the VP of Biological Research and other senior leaders: manage complex calendars and meetings, coordinate travel and expenses, prepare correspondence and presentations, maintain confidential records and office resources, support events and special projects, and partner with administrative staff to ensure smooth departmental operations.

Lead global category strategy and end-to-end procurement for Primary Packaging Injectables. Build annual strategic plans, manage supplier partnerships and negotiations, integrate ESG and supplier innovation, mitigate procurement risk, drive cross-functional projects, and deliver cost, process, and value improvements aligned to business goals.

Lead development and execution of US & Canada regulatory strategies for immunology products. Coordinate FDA/Health Authority interactions, prepare and review regulatory submissions and responses, advise cross-functional teams, and ensure compliance with regulations and corporate policies. Mentor staff and contribute to regulatory planning and implementation.