Part-time
Minimum Qualifications: - Bachelor's Degree preferred. Emphasis on applicants who want to pursue a career in medicine - Bilingual: English/Spanish
Responsibilities: - Clinical trial management, patient communications, document procurement - Management of clinical trial participants, assuring compliance with trial protocols - Communication, planning, and scheduling of meetings and appointments - 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: $24/hr.
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