
10,000+ employees
Founded 2013
🏥 Healthcare
đź’Ľ 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.
🔥 2 minutes ago
🇨🇦 Canada – Remote
đź’µ $130k - $180k / year
⏰ Full Time
đźź Senior
🏥 Clinical Operations
đź‘» Ghost score 0%
Where this job comes from
Posted on AbbVie's careers page, not through a job board
First seen by Remote Rocketship 2 minutes ago

10,000+ employees
Founded 2013
🏥 Healthcare
đź’Ľ 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.
• Support assigned countries and region through implementation and execution of proactive quality management activities • Maintain collaborative relationships with RDQA functions impacting clinical research within designated Affiliates • Establish relationships with clinical development leaders and staff to advance the AbbVie Quality System and achieve first-pass health-authority approval • Oversee quality and compliance in a regulated environment, including AbbVie policies, procedures, and country and regional standards and regulations • Lead or collaborate on risk identification and mitigation/control strategies for clinical research and clinical trials • Establish quality measures and drive quality strategy in designated countries and region • Manage fit-for-purpose governance and oversight under the One AbbVie Quality System • Identify trends, root causes, and risks affecting clinical research • Drive continuous regulatory preparedness and monitor the health of the Quality System with Affiliates R&D Management • Maintain awareness of applicable regulations and develop quality standards for assigned countries and region • Support supplier visits, audits, and vendor qualifications • Develop inspection strategy and provide inspection-readiness support for local and regional Health Authority inspections • Provide oversight, support, and follow-up for Health Authority inspections and participate as needed • Determine need for country/process assessments and audits; conduct audits as required • Communicate audit results orally and in writing • Review and approve corrective action plans and audit responses • Support robust audit and inspection responses through coaching and education • Mentor AREA Managers, AREA Associates, or line management as an additional lead responsibility • Report to the RDQA Associate Director or RDQA Global Director, AREA
• Bachelor's degree required, preferably in Biology, Nursing, Pharmacy, or other medical science degree combined with equivalent technical experience • 8+ years of biopharmaceutical / medical device industry experience in quality assurance, compliance, regulatory affairs, clinical research and/or other related development functions • 3 years in leadership positions (people and/or initiatives/projects) • Strong understanding of local and global regulatory and legal requirements and regulatory agency approaches and perspectives • Ability to ensure strategic risk focus with evolving global regulations and expectations • Agile and able to respond rapidly to unplanned events and changing regulatory requirements and expectations • Thorough knowledge of quality systems, auditing standards and quality management • Strong analytical skills and ability to organize work logically, thoroughly, and succinctly • Ability to work at an experienced level and demonstrate effective leadership with business partners at all levels • Excellent written and oral communication, presentation, and influencing skills • Strong negotiation, influencing, collaborating, and networking abilities • Ability to foster cross-functional collaboration teams • Strong team player or team lead who builds relationships with peers and cross-functionally at global and local levels • Ability to travel as needed in AREA (up to 35%)
• Employees can work remotely • Equal opportunity employer • Travel as needed in AREA (up to 35%)
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