Fortrea·1 day ago
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FSP CRA I/CRA II (Guangzhou)
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About this role
Job Overview. Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the imp...
Skills
- site monitoring
- clinical trial management
- regulatory guidelines compliance
- case report form review
- quality control
- data integrity review
- adverse event reporting
- clinical operations
- clinical trial management system
- vendor management
- registry management
- icg gcp
- iso 14155
- medical terminology
- clinical research processes
- project management
- training and mentoring
- data management
- clinical research operations
- internal communication
- organizational skills
Company
Fortrea
Guangzhou, People's Republic of China
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