01:03

LinkedIn promotion Coordinating clinical research 2024

02:47

Welcome monitoring clinical trials course

01:11

Monitoring Clinical Trials PPT online video for LinkedIn

44:01

Week 1 Introduction to Monitoring narrated

36:31

Week 1 Pathways to Launching a Clinical Research Career

01:03

Monitoring Clinical Trials course at Wake Tech (Raleigh, NC)

29:04

Week 14 Advancing Your Monitoring Skills

35:01

Week 13 Organizing Your Work

18:56

Week 12 Clinical Team Structure and Communication

24:04

Week 11 Protocol Deviations v2

24:37

Week10 Remote Monitoring

22:26

Week 9 PI Oversight

12:15

The Wrap Up 17Sep18

23:53

Week 8 IP and Supplies

25:21

Week 7 Safety and Patient Protection

31:37

Week 6 Source Data Verification

25:10

Week 5 Staff Training and Qualification

30:21

Week 4 Reviewing the Investigator Site File

23:53

Week 3 Conducting Monitoring Visits

25:36

Week 2 Study Startup

44:03

Week 1 Introduction to Monitoring

26:23

How to Land a Job in Clinical Research

13:49

Week 4 Your Next Steps in Clinical Research no interview

22:30

Week 5 Executing Your Plan

14:38

Week 4 Your Next Steps in Clinical Research

24:31

Week 3 Job Roles in Clinical Research

17:29

Week 2 Anatomy of a Clinical Trial

16:48

Scientific Misconduct

05:19

Ethics of Trial Design

34:31

Coding Dictionaries

29:09

EDC systems

28:31

CDMS systems

49:35

Week 11 Cleaning Data Writing and Resolving Queries

39:34

Week 10 MH AE CM and CRF data entry

45:23

Week 9 Entering reviewing data narrated

48:00

Week 9 CRF Design narrated

36:43

Week 7 Subject Recruitment

53:55

Week 6 The Clinical Research Site

06:25

Week 5 Behavior of Investigators Conflicts of Interest

09:45

Week 4 Challenges to IRBs

49:28

Week 1 Intro to Clinical Trials

07:02

Informed Consent in Research

12:01

Good Clinical Practice

41:58

The Data Management Plan narrated v2

47:45

Orientation and Introduction Day 1 narrated

03:40

Week 8 Scientific Misconduct

09:10

Week 7 Challenges to IRBs v2

05:31

Week 5 Special Populations Fall 2015

06:04

Week 3 Informed Consent in Research v3

15:01

Week 3 Good Clinical Practice

08:20

Week 1 History of Regulations

32:06

Week 7 8 Study closeout DB lock

16:17

Week 7 session 2 Scientific Misconduct

37:59

Week 7 session 1 CDISC CDASH

34:19

Week 6 session 1 Coding Dictionaries

29:11

Week 5 session 2 EDC systems Wake Tech PPT

29:54

Week 5 session 1 CDMS systems

46:05

Week 2, Session 2: Entering reviewing data narrated

47:08

Week 2, Session 1: CRF Design

42:06

The Data Management Plan