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Study Management Associate III
hace 2 meses
Job Summary: We are seeking a highly skilled and experienced Study Management Associate III to join our dynamic and centralized study management team at AbbVie. As a key member of the study team, you will be responsible for the execution of our global clinical trials and will work closely with cross-functional partners to plan, execute, and manage Phase 0-4 clinical trials.
Key Responsibilities:
- Provide strategic leadership to cross-functional teams to drive deliverables and timelines for global clinical trials.
- Manage vendor relationships, including Request for Proposal (RFP) initiation, selection, and oversight of external vendors.
- Develop and execute recruitment strategies and mitigation plans on a global scale.
- Lead assigned meetings and provide regular updates on study status.
- Ensure inspection readiness and participate in related activities.
- Identify, mitigate, and manage risks to support trend analysis and risk prevention.
- Develop and manage study materials, including protocols, regulatory submissions, and clinical study reports.
- Manage EDC, IRT, and ePRO systems to ensure compliance and inspection readiness.
- Provide training to stakeholders as needed.
- Support global submission strategies and process improvement initiatives.
Requirements:
- Bachelor's Degree or equivalent required.
- At least 4 years of progressive Pharma-related/clinical research-related experience.
- Strong analytical and critical thinking skills.
- Excellent organizational and time management skills.
- Exceptional interpersonal skills.
- Proactive and collaborative mindset.
- Ability to work independently in a fast-paced global team environment.
