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- Budget Tool Helps Investigative Sites Calculate the Cost of a Coordinator’s Time for a Typical Outpatient Study Visit Part I
- The Role of Data Monitoring Committees and their Impact on Clinical Research Associate Responsibilities
- Recruitment and Retention of Patients and Site Management
- Psychodynamic Influences on Human Subject Recruiting Practices
- Informed Consent or Intuitive Consent?
- Culturally Competent Consent Concepts
- "…in language understandable to the subject…"--or not.
- Informed Consent in Clinical Research
- Risk Overload and Risk Misdirection in the Consent Process
- Why You Shouldn’t Test for Consent Comprehension
- Readability Recommendations: Easier Said Than Done
- Lay Lab Language for Informed Consents
- The HIPAA Privacy Rule and Research
- ERES Compliance and Data Integrity Issues in e-Trials
- Setting Up a Clinical Research Program in the Community Hospital Setting
- End of Life Research
- Budget Tool Helps Investigative Sites Calculate the Cost of a Coordinator’s Time for a Typical Outpatient Study Visit Part I
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- Emergency Clinical Research Symposium
- FDA Clinical Trial Requirements, Regulations, Compliance, and GCP Conference
- Advanced Site Management: Finance and Productivity Enhanced Business Practices for Clinical Research Programs
- Protecting Human Research Participants: Legal, Ethical, and Practical Considerations
- Clinical Investigator GCP & Trials Management Program for Clinical Investigators and Key Research Staff
- Clinical Research Monitoring and GCP Workshop for Monitors, Site Coordinators and Auditors
- Oncology Clinical Trials Conference
- Pediatric Clinical Trials Conference
- Clinical Research Project/Program Management Conference
- Clinical Site Coordinator / Manager and GCP Workshop
- Quality Management through Standard Operating Procedures (SOPs)
- Annual Conference
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- Part I - Informed Consent for Research: Operationalizing the Process
- Part II - Informed Consent for Research: The Importance of Quality for Understanding and Decision-Making
- A Primer on Clinical Research
- Sponsor Responsibilities
- Institutional Review Boards (IRB)
- What You Should Know Before the FDA Arrives
- ICH E6 (R2): From the site’s perspective
- IND / IDE Assistance
- Risk Based Monitoring from the Site Perspective
- cGMP for Investigational New Drugs (IND) in Phase I Clinical Trials
- Regulatory Updates for Clinical Research Professionals - RECERTIFICATION
- Bedside Nursing "Want to Write a Research Protocol?"
- Bedside Nursing "From Clinical Inquiry to Conducting Nursing Research"
- SOCRA YouTube Videos
- OHRP’s Thinking on Key Revisions to the Common Rule
- Creating and Sustaining Diverse Study Enrollment: Towards a Quantifiable Science of Recruitment
- Applying the Principles of the Science of Safety to Improve Subject Safety in Clinical Research: Actionable Practices to Identify and Minimize Risk
- The Evolution of Vulnerability – The Ethics of Equitable Subject Selection
- The Reality of Enrollment Expectations
- Including Vulnerable Subjects with Cognitive Impairment in Research
- Minimally Disruptive Research: A Respectful Approach to Conducting Clinical Studies
- The Evaluation of Evidence for Regulatory Decision Making
- Recent Advances in the Early Detection of Alzheimer's Disease
- E-Consent: Usability Issues
- Informed Consent
- Affordable Care Act and Research: Where Have We Been and Where Are We Going
- An Update from the Patient-Centered Outcomes Research Institute (PCORI)
- Utilizing the Research Ehtics Review Process as a Method to Incorporate Quality by Design
- OHRP’s Thinking on Key Revisions to the Common Rule
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