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About the Role:
- The Study Management Associate III is a key independent contributor responsible for executing Phase 0-4 clinical trials globally.
- This role works closely with the Study Project Manager and cross-functional teams to drive study timelines and quality.
Key Responsibilities:
- Provides strategic leadership to cross-functional teams, manages vendors, and oversees recruitment and study materials.
- Ensures compliance with ICH/GCP and AbbVie policies, and maintains eTMF and CTMS systems.
- Supports global submission strategies and process improvement initiatives.
Qualifications:
- Requires a Bachelor’s degree and at least 4 years of progressive clinical research experience.
- Must have strong analytical, organizational, and interpersonal skills, and proficiency in systems like EDC and IRT.
AbbVie
AbbVie discovers and delivers innovative medicines and solutions for serious health issues across immunology, oncology, and neuroscience. The company is a global biopharmaceutical leader with a focus on making a remarkable impact.