One full-time job and one (32-hour job)
We are looking for two Clinical Trial Coordinators to join our Hematology/Oncology research team. The starting schedule can be flexible, but the person needs to have availability during working hours (e.g. M-F 8-5pm). The person would start at the $24/hr salary. Looking for someone interested in pursuing a career in Medicine. No prior experience required. Spanish proficiency is required.
Duties - 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 be trained) - 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
Experience - Bachelor's degree - Knowledge of clinical development processes and compliance management systems - Familiarity with clinical laboratory procedures and data collection methods - Strong attention to detail and ability to review documentation for accuracy - Excellent organizational skills and ability to manage multiple tasks simultaneously - Ability to work independently as well as part of a team
Salary: $24/hr.