Clinical Research Associate I - The Lundquist Institute

Part-time

Minimum Qualifications: - GED or HS diploma. Bachelor's degree preferred - Emphasis on applicants who want to pursue a career in medicine - Previous experience as a Clinical Research Coordinator or similar role - 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 - Understanding of Good Clinical Practice (GCP) guidelines

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: $24/hr.