Jobs at AbbVie

Lead lifecycle management for medical device software: define requirements, design and implement embedded/Windows applications, integrate and debug hardware/software, execute V&V tests, produce regulated documentation, drive quality and process improvements in compliance with FDA QSR, ISO13485 and IEC 62304.

Lead HEOR strategy and execution for one or more assets/indications, representing HEOR on cross-functional and pipeline commercialization teams. Oversee study design and delivery, align HEOR plans with product strategy, communicate findings to internal and external stakeholders, and ensure partnerships with HEOR centers of excellence. Provide leadership to staff and engage senior management to support regulatory, HTA, and commercial objectives.

Manage account-based market access and contracting for AbbVie oncology portfolio across assigned western US territories. Secure formulary placement and national contract support, develop product positioning and pull-through strategies, lead cross-functional account activities, cultivate executive-level relationships, and coordinate resources to optimize utilization and access.

Lead GMP batch documentation review and disposition for NBE/NCE/ATMP clinical supply. Provide QA oversight of TPMs and manufacturing sites, drive investigations, CAPA, quality agreements, metrics reporting, inspection readiness, and mentor junior PDQA staff to ensure compliance and clinical supply continuity.

Develop and implement LC/MS-based bioanalytical and characterization assays for novel biologics. Operate and maintain mass spectrometers, perform affinity purification and proteomics/immunopeptidomics sample preparation, analyze data, generate reports, optimize assays, and lead scientific efforts to support in vivo PK/TK/PK-PD and stability studies.

Advise cross-functional R&D and business teams on IP matters, develop and implement patent strategies for pharmaceutical products, draft and prosecute patent applications worldwide, work with scientists and outside counsel, and challenge or defend patents in IPRs and other post-grant proceedings.

Lead design, execution, and interpretation of oncology clinical development programs and trials. Oversee study integrity, safety reporting, protocol and regulatory documents, cross-functional alignment, investigator engagement, and mentorship of medical/scientific staff while ensuring GCP and pharmacovigilance compliance.

Field-based oncology nurse educator responsible for providing clinical and product education to allied healthcare teams, developing customized account education plans, supporting infusion administration and adverse event management, documenting clinical insights, collaborating cross-functionally, and delivering presentations at meetings and patient advocacy settings.

Lead design, execution, analysis, and reporting of oncology clinical development programs. Oversee clinical study teams, ensure study integrity, safety reporting, regulatory compliance, and cross‑functional alignment. Serve as clinical expert for molecules/diseases, engage opinion leaders, contribute to translational strategies, and represent AbbVie externally.

Lead and coordinate cross-functional due diligence and search efforts for strategic BD opportunities, manage risks and governance, drive alignment and decision-making, monitor team performance, and support scheduling of external partnering events.

Lead strategic portfolio-insights projects to prioritize R&D investment, refine valuation and PTRS methodologies, benchmark R&D productivity, build value metrics (raNPV, Productivity Index), create executive narratives, support dashboards and data democratization, and drive change management across therapeutic areas and finance to enable data-driven portfolio decisions.

Field-based role supporting BOTOX Therapeutics access by educating providers on reimbursement, payer policies, prior authorization, billing/coding, and patient assistance processes. Identify and resolve access barriers, monitor payer changes, liaise with internal stakeholders, provide analytical, need-based solutions, and support HUB and specialty pharmacy initiatives to improve patient access and outcomes.

Field-based specialist who educates providers on reimbursement, payer policy, prior authorizations, billing/coding, and patient access solutions for BOTOX Therapeutics. Identifies and resolves access barriers, liaises with internal stakeholders, provides analytical need-based solutions, and supports HUB services, appeals, and specialty pharmacy processes.

Field-based pharmaceutical sales role executing brand strategy for psychiatry products. Manage territory and accounts, meet sales/KPI targets, develop and execute call plans, build trusted relationships with healthcare providers and KOLs, gather market intelligence, and ensure HCIR credentialing and compliance. Requires driving, pre-employment screens, and adherence to company policies and regulations.

Lead CMC regulatory knowledge management and strategy by providing guidance, monitoring global trends, maintaining regulatory process documents and portals, advising on submissions, advocating with regulators and industry, championing AI applications, and driving alignment across cross-functional teams to accelerate product development and patient access.

Provide hands-on application configuration, deployment, and integration solutions for R&D scientists. Design system-to-system data workflows, translate functional specs into application designs, collaborate with business analysts and infrastructure/security teams, and support implementation, testing, and change management.

Lead data strategy and study start-up for clinical trials from protocol through system go‑live. Serve as single study data SME, drive standards and data criticality, manage timelines and risks, influence cross-functionally, coach team members, and lead process improvement and innovation.

Provide scientific leadership in developing advanced capillary electrophoresis and chromatographic methods for biotherapeutic protein characterization. Serve as analytical lead on cross-functional CMC teams, supervise scientists, develop/validate and transfer QC and stability methods, support regulatory submissions, and present scientific findings externally.

Lead design, implementation, analysis, and reporting of oncology clinical development programs (Non-Hodgkin Lymphoma). Direct cross-functional teams, ensure study integrity, enrollment, timelines, regulatory compliance, and high-quality scientific output. Serve as in-house clinical expert, engage external opinion leaders, support regulatory interactions, and contribute to translational and business development activities.

Drive adoption and sales growth of Allergan Aesthetics facial products through consultative B2B2C selling, territory business development, cross-portfolio coordination, technical product/procedure expertise, reporting compliance, and achieving assigned sales goals.