Clinical Research Coordinator Mentorship
Come to see how the data is analyzed in the end to understand why the beginnings are so important. One-on-one personalized training during which you will receive coaching sessions and hands-on exercises to excel in the Clinical Research Coordinator career.
| Session 1, 2, 3 |
Session 4, 5, 6 |
Session 7, 8, 9 |
- Introduction to Good Clinical Practice
- Clinical Trials and Protocol Design
|
- Drug and Device development process
- Roles (and Responsibilities) of Sponsors, Investigators, IRBs, Ethics Committee
|
- Study Start-up, and Site Close-out activities, Recruitment, Informed Consent
- Documentation (CRF, EMR, procedure results)
- Data Collection Principles and Tools (e.g. EDC, IXRS blinding)
|
| Session 10, 11, 12 |
Session 13, 14, 15 |
- Safety of Subjects
- What is an Adverse Event and monitoring of Adverse Events
|
- Monitoring reports, queries, visits activities, follow-up visits
- Audit
|
Acronyms:
CRF = Case Report Form
EDC = Electronic Data Capture
EMR = Electronic Medical Record
IRB = Institutional Review Board
IXRS = Interactive Voice/Web Response System
Training Schedule: On demand
- Preferred but not required AA., BA. or BS. degree or min 1 year working as healthcare professional (Medical Assistant, Nursing,
or in a related field)
- Minimum knowledge into the medical field and willingness to put effort into learning new skills.
