Clinical Research Coordinator  (CRC)

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Clinical Research Coordinator  (CRC) by Mind Map: Clinical Research Coordinator  (CRC)

1. Nurses

1.1. Provide and schedule assessments on subjects and also administer study drug. Needs to collect samples and also record important details like start and stop times.

1.2. Written and Verbal communication

2. Clinical Research Assistant

2.1. Helps the clinical research team  and usually has administrative tasks

2.2. Written and Verbal communication

3. Data Manager

3.1. Collects the data needed for  the clinical trial, including collecting data from medical records. Also needs  to be aware of deadlines and address queries coming from study sponsor.

3.2. Written and Verbal communication

4. Research Pharmacist

4.1. Written and Verbal communication

4.2. Responsible for managing the study drug and has to make sure the correct drug is given to the correct participant in blind studies.

5. Research Ethics Board

5.1. Written communication

5.2. REB reviews protocol and all documents that will be given to the patients (ex. consent forms) and reviews product information regarding study drug.

6. Clinical Research Associate               (CRA)

6.1. Written and Verbal communication

6.2. Responsibilities include, making sure study site is ready for the clinical trial to take place, visiting the sites, meeting with investigator and CRC and completing regulatory documentation.

7. Investigator

7.1. Responsible for conduct of the clinical trial at the study site, monitoring the participants and is also the leader of the clinical research team

7.2. Written and Verbal communication

8. Study Participants

8.1. Written and Verbal communication

8.2. Individuals who fit the eligibility criteria and have volunteered to participate in the study

9. Study Manager

9.1. Responsible for overseeing the trial and helping with trouble shooting any issues that may occur during the trial.

9.2. Written communication

10. Regulatory Authorities

10.1. Regulatory bodies such as Health Canada or FDA, who have an associate  that provides support to the clinical trial and who makes sure that the right documentation is available and collected from each study site.

10.2. Written communication

11. Safety Associates

11.1. Responsible for reviewing safety data, including reporting any adverse events reported on participants taking part in the trial

11.2. Verbal and written communication