Jobs at AbbVie

Lead affiliate-wide Customer Excellence across meeting management, learning & transformation, customer engagement, data-driven decision-making and business intelligence. Drive commercial planning, performance management, CRM and digital adoption, cross-functional transformation, and develop a high-performing team to improve execution and measurable business results.

Develop and optimize automated, data-enabled laboratory workflows for early drug development. Responsibilities include HPLC-MS and assay development, physicochemical property profiling, preclinical formulation screening, laboratory automation, workflow optimization, and interpretation of analytical data. The scientist will collaborate cross-functionally with discovery, development, data science, computational chemistry, and informatics teams to advance small molecules, PROTACs, peptides, and other complex modalities.

Leads process excellence and continuous improvement initiatives supporting clinical research processes. Develops process maps and quality system documents, manages stakeholder and impact assessments, coordinates change communications, evaluates metrics, and maintains change management applications. Partners across the Compliance Learning Change Management organization while applying knowledge of AbbVie’s Quality System, GxP regulations, Business Process Framework, and clinical trial systems.

Supports a Vice President and Chief of Staff by managing calendars, communications, travel, expenses, invoices, documentation, office operations, onboarding, and confidential information. Coordinates meetings, site events, culture activities, ERG events, and lab tours while assisting with executive materials and stakeholder relationships. Provides backup support and may train administrative assistants. Requires strong organization, discretion, attention to detail, communication, and Microsoft 365 proficiency.

Drive territory sales for specialty care products by executing sales plans, identifying and expanding business opportunities, maintaining customer records, reporting market intelligence, and representing AbbVie at scientific events. Collaborate with management on forecasts and ensure activities comply with company standards.

Leads early-phase oncology clinical development programs, overseeing trial design, execution, safety, efficacy, data interpretation, regulatory submissions, and study timelines. Provides medical and scientific leadership across global cross-functional teams, investigators, and internal stakeholders. Develops clinical strategies, protocols, and development plans; supports regulatory discussions, business development, translational strategies, and opinion-leader engagement. Ensures compliance with Good Clinical Practices, pharmacovigilance standards, regulations, and company quality procedures.

Supervise pharmaceutical manufacturing shift operations, train operators, oversee critical aseptic production tasks, and maintain SOPs and training programs. Monitor equipment performance, resolve alarms and failures, lead nonconformance investigations and corrective actions, and support quality and EHS audits. Conduct safety audits and Gemba walks, coordinate preventive maintenance, provide performance feedback, and manage raw material inventory and purchasing coordination while ensuring safety, GMP, quality, and production requirements are met.

Leads a global team responsible for clinical process design, change management strategy, continuous improvement, and quality system integration within pharmaceutical R&D. Oversees clinical research process infrastructure, global programs, document architecture, workload prioritization, stakeholder alignment, and team development in a regulated, matrixed environment.

Manages clinical study activities in compliance with ICH/GCP, global regulations, and company procedures. Supports cross-functional study teams, develops protocols and study documents, maintains CTMS updates, oversees vendors, creates training, communicates study status, resolves issues, and contributes to process improvements.

Leads strategic change enablement for clinical development operations and GCP quality systems. Designs clinical research processes, facilitates stakeholder alignment, develops change management and communications strategies, manages supporting systems and global programs, and drives end-user adoption and operational excellence. The role also translates quality regulations, coordinates organizational responsibilities, supports compliance and training initiatives, and assesses performance metrics across a complex matrix environment.

Leads strategic change enablement and continuous improvement initiatives supporting clinical research processes within AbbVie’s GCP Quality Management System. Partners across teams to develop process maps and quality-system documents, assess stakeholders and impacts, manage communications, evaluate metrics, and oversee change-management programs and forums. Requires strong knowledge of pharma or clinical research, GxP regulations, process optimization, change management, and leadership in a matrix environment.

Leads early-phase oncology clinical development programs, including trial design, execution, data interpretation, safety oversight, regulatory submissions, and clinical strategy. Partners with cross-functional teams, investigators, opinion leaders, Medical Affairs, Commercial, and Discovery organizations. Oversees study integrity, timelines, adverse event reporting, protocol development, and compliance with GCP and pharmacovigilance standards. Provides scientific leadership for thoracic malignancies and T-cell engager programs and may supervise medical directors or chair clinical strategy teams.

Field-based medical science liaison supporting AbbVie’s therapeutic-area research and business objectives. Builds relationships with healthcare professionals, thought leaders, researchers, and academic centers; presents scientific and clinical information; supports research initiatives, clinical operations, and investigator projects; answers unsolicited medical questions; trains internal teams; collaborates with commercial partners; documents HCP interactions; and manages territory resources and expenses. Requires travel up to 75% and residence in the assigned territory.

Leads early-phase oncology clinical development programs, including trial design, execution, data interpretation, safety and efficacy oversight, regulatory submissions, and clinical strategy. Partners with cross-functional global teams, investigators, Medical Affairs, Commercial, and regulatory stakeholders. Oversees study integrity, enrollment, timelines, scientific documentation, pharmacovigilance compliance, and clinical development plans. Provides therapeutic expertise in oncology, with thoracic malignancies or T-cell engagers strongly preferred.

Leads business systems and technology capabilities for QA laboratory operations, including sample management, stability studies, reference standards, and lab inventory. Develops multi-year strategies, roadmaps, business cases, and oversees technology project portfolios exceeding $14 million. Partners with IT, manufacturing sites, laboratory stakeholders, and vendors to implement scalable, compliant solutions. Manages financial objectives, timelines, team workload, performance, hiring, and succession planning.

Leads early-phase oncology clinical development programs, including trial design, execution, oversight, data interpretation, safety reporting, regulatory submissions, and clinical strategy. Coordinates cross-functional global teams, investigators, study personnel, and opinion leaders while ensuring compliance with Good Clinical Practices, pharmacovigilance standards, and regulatory requirements. Provides medical expertise for assigned molecules and disease areas, supports translational strategies and business development, and may supervise medical or scientific directors.

Leads the strategy, design, execution, interpretation, and reporting of oncology clinical development programs from Phase 1 through Phase 3. Oversees clinical study teams, safety and efficacy assessments, regulatory submissions, investigator engagement, study integrity, enrollment, and timelines. Serves as a clinical expert, collaborates with cross-functional global teams and external opinion leaders, supports translational and business development activities, and ensures compliance with Good Clinical Practices, pharmacovigilance standards, and regulatory requirements.

Leads process and equipment design for strategic capital projects in drug product manufacturing or packaging. Drives design decisions, equipment specifications, risk management, project controls, procurement strategy, regulatory audit readiness, and cost-effective technical solutions. Collaborates with internal teams and external consultants, represents engineering on task forces, and may supervise engineers or technicians while ensuring compliance with cGMP and applicable policies.

Independently designs, executes, interprets, and optimizes scientific experiments and laboratory methods. Develops experimental protocols, applies scientific literature, masters new techniques, mentors colleagues, manages timelines, and presents scientific data. Contributes to publications, presentations, and patents while supporting manufacturing needs and responding to time-sensitive operational challenges. The role requires expertise in HPLC, capillary electrophoresis, AKTA-based protein purification, and ELISA assays.

Develop and maintain Linux-based C/C++ software for peptide array synthesizers and laboratory instruments. Integrate sensors, actuators, pumps, motors, cameras, and other devices; conduct testing, validation, troubleshooting, experiments, and system characterization. Support instrument deployment and operation while collaborating with scientists, hardware engineers, quality, operations, and IT teams. Lead technical initiatives, mentor engineers, and deliver compliant, reliable software using Agile practices.