Assistant Clinical Research Coordinator

Om Research LLC

Lancaster, CAFull-time

Behavioral Health Market Context

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Job Description

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 Assistant 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. Training subjects on protocol expectations

7. Performing study/protocol procedures in a detailed and accurate manner

8. Maintaining study files

9. Tracking subjects, avoiding lost-to-follow-up's

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

Knowledge of Spanish and / or Phlebotomy training will be an added advantage.

Qualifications

  • Knowledge of Spanish and / or Phlebotomy training will be an added advantage

Responsibilities

  • 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 Assistant Clinical Research Coordinator include:
  • Preparing for study initiation
  • Obtaining physician signatures
  • Screening and scheduling subjects
  • Getting voluntary subject consent
  • Training subjects on protocol expectations
  • Performing study/protocol procedures in a detailed and accurate manner
  • Maintaining study files
  • Tracking subjects, avoiding lost-to-follow-up's
  • 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


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