Institutions
Does This Study Require IBC Review?
While clinical research professionals are familiar with the role of the IRB to protect research subjects, most are unfamiliar with the added need for an Institutional Biosafety Committee (IBC).
Decentralized Recruiting, Enrollment, and Participant Engagement with a CTMS
Watch our webinar highlighting a CTMS' capabilities to streamline research, facilitate compliance, and enhance the participant experience.
4 Questions to Ask When Evaluating Your Research ROI
Return on investment (ROI) is a critical metric for clinical research leadership. Read more for questions to ask as you evaluate your ROI.
Future of Work in Clinical Research
When SARS-CoV-2 (the virus causing the disease COVID-19) broke out in 2020, the clinical research community needed to pivot quickly...
Connecting Patient Centricity and eConsent Together
eConsent is a way to enhance the patient experience through improved study design, retention rates, and communication.
Advarra Trend Report: The Future of Work in Clinical Research
Download our report to learn more how the COVID-19 pandemic impacted the future of the clinical research workforce.
Encouraging Site Centricity and Collaboration at Onsemble
At the 2021 Fall Onsemble Conference, attendees learned about putting site centricity and collaboration at the helm of research operations.
Screen Failure in Clinical Trials: Improving Reconciliation
Learn how screen failures occur and which three things to improve reconciliation can be done by those who manage clinical research.
Leveraging Data to Lead and Manage the Research Mission
This blog discusses how to use clinical data at all levels to lead and drive the research enterprise and day-to-day operations
Clinical Research Staffing Reprioritizations and Resourcing Strategies
Gain insights on how to work through staffing reprioritizations and options to consider when planning resourcing strategies.
Budgeting and Billing Compliance in Study Activation
From making do with a tight budget to taking less conventional approaches, learn how you can ensure that reliable timelines are maintained.
Beginner’s Guide to Compliant Electronic Source Data Capture
Learn about electronic source data capture in clinical trials, relevant regulations, and best practices.
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