Clinical Affairs Specialist
Abbott Laboratories(1 month ago)
About this role
The Clinical Site Operation (In‑house CRA) is responsible for managing study documentation and operational progress using a Clinical Trial Management System, ensuring clinical studies comply with applicable regulations and SOPs. The role supports clinical investigations, post‑marketing surveillance, and research across the Medical Devices division while collaborating with APAC and global partners. It leverages prior CRA experience to provide broader study oversight and contribute to process improvements and future leadership pathways.
Required Skills
- CTMS Management
- Study Management
- Document Development
- Inventory Management
- Vendor Management
- Clinical Monitoring
- GCP
- ISO14155
- Microsoft Office
- Communication
+5 more
Qualifications
- Bachelor's Degree
- Science/Health Degree
About Abbott Laboratories
abbott.comInnovative medical devices and health care solutions for cardiovascular health, diabetes management, diagnostic testing, nutrition, chronic pain and more.
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