- 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 :
- Bachelors Degree or equivalent degree is required
- 8 years of 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 5 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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Work :
No
Employment Type :
Full-time