Clinical Research Associate

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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