Assistant Clinical Research Coordinator

Om Research•Camarillo, CA

About The Position

The Assistant Clinical Research Coordinator comprises an integral part of the research team. Working under the PI, he/she is responsible for conducting the study in accordance with federal regulations. Some responsibilities of the Clinical Research Coordinator include: 1. Preparing for study initiation 2. Obtaining physician signatures 3. Recruiting subjects 4. Screening and scheduling subjects 5. Getting voluntary subject consent 6. Teaching subjects about protocol expectations for them 7. Performing study/protocol procedures in a detailed, accurate manner 8. Maintaining study files 9. Tracking subjects, avoiding lost-to-follow-up 10. Documenting an adverse event 11. Processing and shipping lab work 12. Maintaining communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel 13. Completing case report forms (CRF's) for PI review and approval 14. Helping study monitors with CRA corrections 15. Maintaining study-specific supplies 16. Preparing for study closure and archiving

Nice To Haves

Knowledge of Spanish
Phlebotomy Training

Responsibilities

Preparing for study initiation
Obtaining physician signatures
Recruiting subjects
Screening and scheduling subjects
Getting voluntary subject consent
Teaching subjects about protocol expectations for them
Performing study/protocol procedures in a detailed, accurate manner
Maintaining study files
Tracking subjects, avoiding lost-to-follow-up
Documenting an adverse event
Processing and shipping lab work
Maintaining communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel
Completing case report forms (CRF's) for PI review and approval
Helping study monitors with CRA corrections
Maintaining study-specific supplies
Preparing for study closure and archiving