Jobs at AbbVie

Lead execution and oversight of commercial strategic initiatives, build and maintain executive dashboards, produce leadership-ready presentations and analyses, drive cross-functional project planning, monitor KPIs and risks, translate data into actionable recommendations, and ensure accountability and operational excellence across programs.

Field-based specialist who supports HCPs on patient access and reimbursement for AbbVie Eye Care products. Educates providers on payer policies, coding, specialty pharmacy/distribution, and patient support programs; liaises with Access and Reimbursement support center; monitors payer trends; and builds local provider relationships to resolve access issues.

Lead payer and pricing strategy for AbbVie27s Eye Care portfolio across commercial, Medicare, Medicaid and VA channels. Drive market access plans, HEOR/RWE alignment, LRP/Plan/LBE forecasting, and launch strategy for gene therapy SuraVec, coordinating cross-functional stakeholders and payer policy engagement.

Lead clinical data systems for therapeutic areas: manage technology evaluations/implementations, supervise and develop staff, own processes and standards (CDASH/SDTM), support database design, provide strategic direction and cross-functional coordination to improve performance and cost.

Designs, develops, and improves packaging products/processes for pharmaceutical/healthcare products. Plans and executes small-to-medium engineering projects, creates design specifications, validation protocols, and RCEs, mentors technicians, coordinates resources, and ensures compliance with policies and quality standards.

Lead global regulatory strategy and teams to secure and maintain product approvals across development and post-approval lifecycle. Develop regulatory dossiers and messaging, anticipate and mitigate risks, interface with cross-functional stakeholders and agencies, influence regulatory policy, present recommendations to senior management, manage budgets and resources, mentor regulatory staff, and drive alignment of global regulatory activities with business objectives.

Designs and delivers clinical trial systems (EDC, IRT, ePRO) ensuring standards (CDASH/SDTM), regulatory compliance, integrations, program consistency, mentoring, and process improvements.

Lead and coordinate field commercial teams to meet sales targets in an assigned territory. Develop and execute district sales plans, coach and mentor direct and indirect reports, drive market and franchise strategy, collaborate with internal partners on business planning, ensure HCIR credentialing and compliance, and manage day-to-day field execution.

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.

Field-based pharmaceutical account specialist responsible for driving hospital and institutional adoption of anti-infective products. Builds relationships with hospital, IDN, outpatient and specialty accounts; executes account-based plans; navigates formulary, buy-and-bill and specialty pharmacy channels; collaborates cross-functionally with MSLs and account leaders; presents on-label clinical/operational value propositions; meets sales targets while maintaining HCIR credentialing and travel requirements.

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.

Develop and maintain software for embedded, regulated devices, conduct system analysis, collaborate with teams, and ensure quality in software solutions.

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

The Supervisor will ensure compliance in cross-border transactions, assign tariff classifications, implement technology solutions, manage documentation, and lead training on trade compliance.

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.

Provide financial leadership for planning processes, prepare accurate financial reports, support executive decision-making, and lead finance transformation initiatives while managing and coaching staff.

The Director oversees HEOR strategies for oncology, directing projects, engaging with stakeholders, and supporting market access and commercialization activities.

The Asset Strategy Leader directs the asset lifecycle from discovery to commercialization, guiding strategy across various teams and ensuring alignment with enterprise objectives, while leading a cross-functional strategy team and interfacing with senior governance.

This role leads clinical studies for product development in aesthetics, ensures data integrity, collaborates with teams, and oversees regulatory compliance.

The MSL role focuses on strategic support for research and business goals in oncology, building relationships with experts, communicating insights, and executing territory plans. Candidates should educate themselves on market trends and comply with corporate policies while meeting travel requirements.