A company is looking for a Central Study Coordinator in Mexico.
Key Responsibilities
Coordinate and support remote site activities for assigned projects
Serve as the point of contact for day-to-day site communications and document submissions
Perform data entry and monitor clinical databases as assigned
Required Qualifications
Bachelor's degree or equivalent experience with a minimum of 2 years of related experience
Current knowledge of ICH / GCP and applicable regulations and guidelines
Ability to manage technology and web-based research platforms
Experience working in a study team environment is ideal
Competent in standard business procedures, including SOPs and global regulations
Study Coordinator • Odessa, Texas, United States