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AbbVie
AbbVie
15 open remote positions
AbbVie is a pharmaceutical company dedicated to discovering and delivering innovative medicines in immunology, oncology, and neuroscience. As a large global organization, it employs thousands and operates with a culture of integrity and innovation.
Salary Distribution
4 of 15 jobs
Benefits Overview
13 of 15 jobs
401(k)
(13)
Dental
(13)
Medical
(13)
Vision
(13)
PTO
(12)
Long-term Incentive
(3)
Long-term incentive
(1)
Paid Time Off
(1)
Open Positions
Lead a regional team of Field Reimbursement Managers to deliver compliant access and reimbursement support for oral migraine therapies. Partner cross-functionally with Sales, Patient Services, and Market Access to align field execution and identify access barriers. Ensure accurate, compliant customer education on coverage, coding, billing, and affordability for AbbVie products.
Market Access
Reimbursement
Leadership
Team Management
Compliance
Execute brand strategy and sales performance to maximize short and long term results. Build trusted customer relationships and effectively manage territory and accounts. Differentiate AbbVie’s value proposition and maintain disease state experts to drive brand performance.
Sales
Pharmaceutical
Customer Relationship Management
Business Acumen
Strategic Thinking
Define and evaluate security architecture for end-user devices, including workstation hardening, EDR, and data protection. Advise on mobility security for MDM/UEM, mobile application management, and BYOD posture across iOS and Android. Perform security architecture reviews, deliver consulting engagements, and create reusable security artifacts.
Endpoint Security
Security Architecture
Risk Management
AI Tools
Acts as primary point of contact for investigative sites, providing training and support to ensure compliance with protocols and regulations. Conducts site evaluation, monitoring, and closure activities while managing recruitment and retention plans based on patient journey. Collaborates with central monitoring to assess risks and ensure data quality, safety reporting, and audit readiness at assigned sites.
Clinical Research
Regulatory Compliance
Customer Relationship Management
Project Management
Proactively engage with allied healthcare professionals to provide product and disease education for patient management on approved therapies. Educate patient care teams on infusion processes, adverse event management, and patient diagnosis in a defined geographical region. Collaborate with field teams and internal functions to support clinical education and training initiatives.
Clinical Education
Oncology
Nursing
Communication
Cross-functional Collaboration
Provides study-level oversight and leadership for global clinical trials from inception through closure, managing vendors, recruitment, and cross-functional teams. Develops and manages study materials including protocols, regulatory submissions, and budgets while ensuring compliance with quality standards and inspection readiness. Contributes to system management like EDC, IRT, and eTMF, and supports process improvement initiatives or serves as a mentor.
Clinical Research
Project Management
Vendor Management
Regulatory Compliance
Data Analysis
Serve as the primary point of contact and partner with investigative sites to ensure high-quality clinical trial conduct. Conduct site evaluation, training, monitoring, and closure activities in compliance with regulations, GCPs, and SOPs. Utilize risk-based monitoring and site engagement strategies to improve data integrity, compliance, and study performance.
Clinical Research
Monitoring
GCP
Regulatory Compliance
Cross-functional Collaboration
Manage all aspects of designated national and regional educational programs for the advanced/faculty customer segment, from concept refinement to cross-functional execution. Lead digital content for AMI Online, driving campaigns to enhance registrations through SFMC and optimizing user experience in collaboration with international teams. Ensure budget and compliance management, including monthly reporting and working with Medical and Regulatory stakeholders for material approvals.
Project Management
Budget Management
Cross-functional Collaboration
Microsoft Office Suite
Lead strategy for HCV thought leader engagement and market differentiation. Manage a team of regional Thought Leader Liaisons to execute in-field marketing plans. Collaborate cross-functionally with sales, marketing, and medical affairs to drive business results.
Marketing
Sales
Project Management
Strategic Planning
Market Research
Identify and maintain professional relationships with thought leaders and researchers to provide scientific support. Present scientific information on disease states and AbbVie products to healthcare professionals. Support research initiatives and collaborate with internal teams to achieve business objectives.
Medical Affairs
KOL Management
Cross-functional Collaboration
Territory Management
Coordinate in-field commercial activity to achieve sales targets within the assigned geography. Coach, mentor, and develop team members to enhance skills and elevate overall performance. Create and communicate the District Sales Plan while monitoring progress and aligning with business goals.
Pharmaceutical Sales
Business Analysis
Leadership
Strategic Planning
Managed Care
Execute high-impact territory plans and build relationships with external experts. Serve as a scientific resource and educate healthcare providers on disease states and products. Support research initiatives and collaborate with cross-functional field teams.
Clinical Research
Scientific Communication
Relationship Management
Data Analysis
Problem Solving
Educate healthcare providers on patient support programs, including access and reimbursement tools and services. Provide local expertise on payer policies, coding changes, and claims submission processes to improve patient access. Liaise with AbbVie's Access and Reimbursement support center to update providers on prescription status and program eligibility.
Presentation
Business Acumen
Strategic Thinking
Leadership
Leads writing and preparing clinical and regulatory documents for drug and device development. Coordinates review, approval, and quality control across functions to ensure compliance and timelines. Develops knowledge of US and international regulations and participates in process improvements.
Medical Writing
Clinical Research
Regulatory Submissions
Data Analysis
Project Management
Lead and develop a team of Thought Leader Liaisons to shape external expert engagement strategies for Multiple Myeloma. Foster relationships with national and regional oncology hematology experts to inform brand decisions and strengthen the thought leader base. Partner cross-functionally with marketing, medical affairs, legal, and compliance to execute compliant engagement activities.
Leadership
Cross-functional Collaboration
Strategic Planning