
10,000+ employees
Founded 2013
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.
🔥 15 hours ago
🌽 Illinois – Remote
💵 $160.5k - $305k / year
⏰ Full Time
🟠 Senior
📋 Program Manager
🦅 H1B Visa Sponsor
👻 Ghost score 0%
Where this job comes from
Posted on AbbVie's careers page, not through a job board
First seen by Remote Rocketship 15 hours ago
Still open on AbbVie's site. Checked 1 hour ago.

10,000+ employees
Founded 2013
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.
• Serve as a strategic advocate for pipeline assets and connect clinical science with operations to execute clinical research programs • Develop clinical operational strategies aligned with asset strategy and oversee clinical study/program execution • Generate operational timelines and enrollment options, assess patient-population availability, and balance trial complexity against speed • Evaluate programmatic risks and mitigations and identify strategic options for asset teams • Influence management and cross-functional teams to achieve program objectives • Contribute to portfolio planning, including clinical-development costs, resource projections, and timelines • Review and provide clinical-operations content for clinical and regulatory documents, including INDs, IBs, NDAs, BLAs, MAAs, and regulatory briefing books • Manage external budgets across portfolios ranging from $20 million to $200 million • Lead large-scale cross-functional innovation and process-improvement initiatives and manage change • Develop, manage, mentor, and supervise clinical-operations staff, including 4–15 study managers and up to 30 indirect staff • Execute clinical programs in compliance with ICH/GCP, global regulations, and AbbVie policies and procedures
• Bachelor’s degree or equivalent, typically in nursing or a scientific field; an Associate’s degree/R.N. or equivalent with relevant experience is acceptable • 12+ years of pharma-related or clinical-research-related experience and/or applicable work experience • 10 years of clinical research and/or applicable work experience demonstrating core, technical, and leadership competencies • Experience setting and driving study strategy and leading a global team in managing and completing multiple clinical studies • Experience in risk management, decision-making, and strategic execution • Good communication skills • Successful coaching, mentoring, and people-management experience; remote-management experience preferred • Subject-matter expertise in standard business procedures, including ICH, global regulations, ethics, and compliance • Participation in clinical-operations initiatives or advancement of clinical-operations strategies • Experience from study initiation through completion, primary data analysis, and/or multiple study phases (Phase 1–3, 4)
• Paid time off (vacation, holidays, sick) • Medical, dental, and vision insurance • 401(k) • Eligibility to participate in long-term incentive programs • Equal opportunity employer • Reasonable accommodations for applicants with disabilities
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