About the job
Purpose
Join AbbVie as a Study Management Associate III and become an integral member of our vibrant, centralized study management team. You will play a pivotal role in the execution of global clinical trials, collaborating closely with the Study Project Manager and SMA Manager to ensure the highest quality and efficiency in our studies.
As a Study Management Associate III, you will independently lead and contribute within a global, cross-functional team to manage one or more Phase 0-4 clinical trials. Your expertise will ensure these studies align with AbbVie’s strategic objectives while adhering to timelines and budgets. This position may allow for virtual work, offering flexibility and convenience.
Responsibilities
- Lead and oversee global clinical trials, ensuring compliance with quality standards, including ICH/GCP and AbbVie policies.
- Support the Study Project Manager in strategic team leadership, stakeholder engagement, and timely execution of clinical trials.
- Manage vendor relationships, including RFP initiation, selection, and deliverable oversight.
- Develop and execute recruitment strategies while managing risk and ensuring subject retention.
- Conduct meetings with stakeholders and provide regular updates on study status.
- Ensure inspection readiness and participate in related activities, including risk identification and management.
- Co-develop and manage essential study materials such as protocols and regulatory submissions.

