About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com.
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Your Role
Lead high-performing clinical research teams to accelerate AbbVie’s pipeline and bring innovative therapies to patients. As a Clinical Operations Manager, you will drive clinical trial excellence through strategic leadership, operational oversight, and strong partnerships with research sites, investigators, and cross-functional stakeholders.
You will be accountable for study delivery, team performance, resource optimization, and quality execution while positioning AbbVie as a trusted partner in clinical research.
Key Responsibilities
- ✓Lead, develop, and coach Clinical Research Associates and site-facing teams to deliver outstanding performance.
- ✓Drive the successful execution of clinical trials, ensuring delivery on time, within budget, and in compliance with quality standards.
- ✓Provide strategic oversight of study planning, feasibility, resource allocation, and risk management.
- ✓Build strong partnerships with investigators, KOLs, research sites, Medical Affairs, Commercial, and R&D stakeholders.
- ✓Foster a culture of continuous improvement, innovation, accountability, and collaboration.
- ✓Ensure compliance with ICH-GCP, local regulations, and AbbVie policies, maintaining audit and inspection readiness.
- ✓Leverage data and performance metrics to identify opportunities, mitigate risks, and improve operational outcomes.
- ✓Lead and support local and global initiatives that enhance clinical research capabilities and accelerate pipeline delivery.
Qualifications
- ✓Bachelor's degree in a health-related field (Life Sciences, Pharmacy, Nursing, Medicine, or equivalent).
- ✓Minimum 3 years of clinical monitoring experience.
- ✓Proven people leadership experience, including coaching, mentoring, and performance management.
- ✓Strong knowledge of ICH-GCP, clinical trial operations, and applicable regulatory requirements.
- ✓Experience managing multiple studies, therapeutic areas, and/or phases of clinical development.
- ✓Strong stakeholder management, communication, and influencing skills.
- ✓Demonstrated ability to navigate complexity, ambiguity, and evolving business priorities.
- ✓Track record of driving continuous improvement, operational excellence, and innovation.
- ✓Strong organizational skills, decision-making capability, and a proactive, solutions-oriented mindset.
- ✓Ability to build trusted partnerships and inspire high-performing teams.
Join AbbVie and help transform groundbreaking science into life-changing medicines.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html