Please create a high-level masters level PowerPoint (15 slides) with speaker notes on each slide for the following 2 questions 1. What are the characteristics of successful investigators and others...

Running Head: HEALTHCARE PRESENTATION                        1
HEALTHCARE PRESENTATION                                10
HEALTHCARE PRESENTATION
Table of Contents
Slide 1: Title    3
Slide 2: Clinical Investigator    3
Slide 3: Characteristics of Clinical Investigator    3
Slide 4: Conducting Ethical Research    4
Slide 5: Process of Informed Consent    4
Slide 6: Following the Policies and Standards    5
Slide 7: Following the Policies and Standards (Continued)    5
Slide 7: Supervising    6
Slide 8: Adverse Event Reporting    6
Slide 9: Keeping Accurate Records    7
Slide 10: Clinical Research Manager and its Work    7
Slide 11: Research Tasks are Delegated    8
Slide 12: The Extensive Research Group    8
Slide 13: Increasing Employee Satisfaction    9
Slide 14: Increasing Employee Satisfaction (Continued)    9
Slide 15: Preparing for Employee Turnover    10
Slide 16: References    11
Slide 1: Title
PROJECT MANAGEMENT AND LEADERSHIP FOR CLINICAL RESEARCH
Slide 2: Clinical Investigato
· In charge of making sure that a research is ca
ied out in accordance
· With the signed investigator statement
· In charge of safeguarding the well-being, safety and rights
A clinical investigator is someone who is in charge of making sure that a research is ca
ied out in accordance with any applicable rules, the investigational plan and the signed investigator statement. They are in charge of safeguarding the well-being, safety and rights of those in their care, as well as the control of medicines under investigation.
Slide 3: Characteristics of Clinical Investigato
· Conducting Ethical Research
· Process of Informed Consent
· Following the policies and standards
· Supervising
· Adverse Event Reporting
· Keeping accurate records
Clinical investigators confront problems that differ from those faced in ordinary medical practice. Many of these issues arise as an outcome of the rigor of clinical trials and regulatory constraints. The fundamental obligation of a clinical investigator is to conduct research that contributes to generalizable knowledge while safeguarding the welfare and rights of human subjects. Clinical investigators must follow all research standards, including the Good Clinical Practice Guidelines and regulatory criteria, when conducting a clinical study (Wake Health, 2022).
Slide 4: Conducting Ethical Research
· Investigators must be vigilant
· Research must be conducted ethically
· Investigator must be responsible equitable and fai
· They must evaluate the protocol
The Belmont Report of 1979 set fundamental rules aimed at preventing ethical issues in research. Throughout the course of a clinical study, investigators must be vigilant. There are a number of regulatory protections in place to guarantee that research is conducted ethically.
The investigator is ultimately responsible for ensuring that the research is equitable and fair to study participants. Clinical investigators must thoroughly evaluate the protocol and be aware of the study's primary end-point (Wake Health, 2022). This technique avoids unintended consequences that might jeopardize the study's scientific integrity or patient safety.
Slide 5: Process of Informed Consent
· Investigator must inform participants about study
· Must be familiar with the possible side effects and advantages
· Give freedom to make informed decisions
Individuals participating in clinical research must be properly informed about the study they are being given. A qualified individual who is familiar with the possible side effects and advantages of the therapeutic agent and knows the clinical trial protocol under study must perform an adequate informed consent procedure (Wake Health, 2022).
Individuals must be given the chance to make informed decisions about the ways, in which they will be treated and the treatments, in which they will engage. The informed consent document is a record of the information that was discussed throughout the informed consent procedure.
It is critical that study participants sign the most recent approved version of the form for the trial, in which they are taking part. To avoid mistakes, several sites use "version control", which involves keeping an electronic file of informed consent forms (Wake Health, 2022).
Slide 6: Following the Policies and Standards
· Investigator must follow all...