Job Description
* Defines and drives the study level operational strategies and deliverables – linking these to asset level goals
* Brings strategic, asset level thinking and innovative problem solving to study planning and execution
* Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures).
* Effectively present and contribute to discussions on study operations at asset level strategic meetings
* Leads clinical operations planning through to execution via cross functional matrix environment and influences cross functional stakeholders to drive milestone achievement
* Demonstrates the skills, experience and critical thinking to lead cross functional teams with minimal supervision.
* Expertise in end-to-end clinical study operations management (all phases, set up to close out)
* Coaches and mentors team members, delegates and empowers to the right level, actively contributes to Development Operations community
* Demonstrates leadership with high level cross functional stakeholder management and influencing skills
* Lead operational efficiencies and foster a culture of innovation
Qualifications
* Bachelor’s Degree or equivalent degree is required
* Extensive demonstrated pharma-related and/or clinical research related experience or equivalent required.
* Exposure in study initiation through study completion in Phase 1-4 and/or Medical Device Trial Experience.
* No direct reports, but matrix management.
* Required experience in Project Management interventional trials
* Experience in Oncology studies in the last years of experience.
* Homebased.
Additional Information
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.
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