Contents;
- How to Launch a Successful Career in Clinical
Research: Tips on Making the Most of Available
Resources
- Institutional Review Board Approval
- Writing Informed Consent Documents
and Obtaining Informed Consent
- Ethics of Data Sharing and Handling
of Genetic Information
- Writing a Statistical Analysis Plan
- Protocol Implementation Procedures
- Screening and Evaluation
- Recruitment and Retention
- How to Set up Your Database
- Budgeting Process and Management
- Understanding Food and Drug Administration
(FDA) Regulatory Requirements for
Investigational New Drug Applications (IND)
for Sponsor-Investigators
- Data and Safety Monitoring