Minimum Qualifications:
Responsibilities:
Coordinate and oversee clinical research studies from start to finish
Ensure compliance with all applicable regulations and guidelines
Manage study documentation, including informed consent forms and study protocols
Collect and record data accurately and in a timely manner
Perform phlebotomy as needed (will receive training once hired)
Review and verify documentation for accuracy and completeness
Monitor patients throughout the duration of the study
Maintain a high level of quality control and data integrity
Adhere to Good Clinical Practice (GCP) guidelines
Salary: $25/hr.
Clinical Research Associate I • Torrance, CA
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