Assistant Clinical Research Coordinator | Oxnard, CA

Detailed Information

  • Location: Camarillo, CA

  • Company: OM Research

subjects4. Screening and scheduling subjects5. Getting voluntary subject consent6. Teaching subjects about protocol expectations for them7. Performing study/protocol procedures in a detailed, accurate manner8. Maintaining study files9. Tracking subjects, avoiding lost-to-follow-up10.

Documenting an adverse event11. Processing and shipping lab work12. Maintaining communication and correspondence (by telephone, email, fax, etc. ) with subjects, sponsor, monitor and other site study personnel13. Completing case report forms (CRF's) for PI review and approval14. Helping study monitors with CRA corrections15. Maintaining study-specific supplies16. Preparing for study closure and archiving Knowledge of Spanish and / or Phlebotomy Training will be an added advantage.

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