CDM Interview Preparation/Mock Interview

1) Safety and Patient Protection
2) Subject Recruitment
3) The Clinical Research Site
4) Therapeutic Areas
5) Monitoring of Clinical Trials
6) Organizing Your Work Clinical Monitor
7) Staff Training and Qualifications
8) Clinical Team Structure and Communication
9) Pre-Clinical Studies
10) Preclinical drug development
11) Types of Clinical Studies
12) Types of Study Designs
13) Blinding vs Randomization Process
14) Types of Clinical Data
15) Drug Regulatory Bodies in Different Countries
16) IRB and its Role
17) Drug Development Process
18) Drug Development Process all images
19) Protocol
20) Study protocol_examples_completed
21) Medical History, Adverse Events, Concomitant Medications
22) Protocol Deviations
23) Case Report Forms 
24) Case Report Forms (Design of CRF)
25) Case Report Form (CRF) Design
26) Case Report Forms -(How To Review a  CRF Statistical) 
27) EDC SYSTEMS
28) Electronic Data Capture_Medidata Rave
29) CDM Documents
30) Data Management Plan
31) Source Data Verification
32) Discrepancy Management
33) Cleaning Data – Query Writing and Resolving Queries
34) Data issues log for cross-functional teams 
35) Study Startup
36) Study Conduct and  Close Out and Submission
37) Data Reconciliation
38) Adverse Events vs Adverse Drug Reactions_completed
39) Serious Adverse Event Reconciliation
40) Coding Dictionaries
41) Laboratory Data Management
42) Local-Lab-vs-Central-Lab
43) Study Close-Out and Submission
44) How to Create Edit Checks
45) Edit Checks
46) User Acceptance Testing (UAT)