April 22nd 2025
Strategies for ensuring that innovation with PROs remains parallel with advancements in disease detection and progression.
April 11th 2025
Examining the implications of the recent US executive orders concerning diversity, equity, and inclusion pursuits—and the key questions each clinical trial stakeholder must now navigate.
April 10th 2025
The future of clinical trial design involves incorporating the patient experience into strategic asset planning.
April 9th 2025
Anticipating divestment, reallocation of investments, and retrenchment.
April 8th 2025
Why investing in truly effective training from the outset can pay off exponentially for clinical teams—and serve as a strategic advantage.
Virtual Sites—Are they the Future of RWE?
Webinar Date/Time: Wednesday, March 29th, 2023 at 11am | 8am PDT | 4pm BST | 5pm CEST
Ancillaries are simple, right? Think again.
Webinar Date/Time: Wednesday, March 29, 2023 at 11am ET |10 am CT | 8am PT
WiFi Automation Keeps Decentralized Clinical Trials Running
Reliable internet connection an integral part of movement to DCTs.
eConsent for Modern Clinical Trials: How to Deliver Engaging, Compliant and Interactive Remote Consent
Webinar Date/Time: Tuesday, March 21st, 2023 at 9am EDT | 6am PDT | 1pm GMT | 2pm CET
The Benefits and Limitations of Clinical Data Platforms
Considerations to help tailor new tools as part of a custom clinical trial strategy.
SCOPE 2023: Concerns for Clinical Operations Professionals in 2023
Melissa Easy, VP and GM, clinical technologies at IQVIA speaks about what should be top of mind for clinops professionals in 2023 at the SCOPE 2023 conference in Orlando, FL.
SCOPE 2023: Synopsis of Biospecimen Sample Management Presentation
Hope Meely, chief clinical officer at Slope, provides a brief summary of her SCOPE presentation revolving around biospecimen collection.
SCOPE 2023: Biospecimen Presentation Questions & Insights
Hope Meely, chief clinical officer at Slope, discusses the feedback she received following her SCOPE presentation around biospecimen collection.
A Singular Root Cause Undermines Clinical Trial Success: Leveraging Best Practice from 50 Years of Applied Research
Researchers face various challenges that cause their clinical trials to fail to meet enrollment timelines, among other issues.
Shifting Data Closer to the Patient
Webinar Date/Time: Thursday, March 30th, 2023 at 10am EDT|7am PDT|3pm BST|4pm CEST
At-home Self-collection of Blood Specimens for Safety Lab Testing in Clinical Trials via the Tasso+ Device
Laboratory services organization focuses on easing patient and site burden with improved collection device.
How to Make Your Rare Disease Trials More Patient and Site-Centric
Webinar Date/Time: Thu, Mar 9, 2023 11:00 AM EST
Reviewing FDA’s Proposed IRB and Informed Consent Rule Changes
21st Century Cures Act prompts FDA to harmonize regulations.
Phesi Report: Assessing Single Patient Investigator Sites in Cancer Clinical Trials
Already existing enrollment challenges emphasized by single patient sites.
Top Considerations for IRT Audit Data Management
Webinar Date/Time: Tue, Feb 21, 2023 11:00 AM EST
Applied Adaptive Design Using Subgroup Identification & Machine Learning
Webinar Date/Time: Tue, Mar 14, 2023 11:00 AM EDT
Novel CRA Training Methods Emerge
Tim Bray, chief sourcing and training officer at Virb discusses how CROs and sponsors can mitigate risks by onboarding CRAs with less experience.
How Mobile Nursing is Evolving to Meet the Stringent Demands of Today’s Decentralized Clinical Trials
Webinar Date/Time: Thu, Jan 26, 2023 11:00 AM EST
An Examination of the Role of the Clinical Research Associate and Factors Impacting Performance and Experience
Study by Tufts CSDD uncovers potential reasons behind CRA shortages, turnover, experience requirements, and more.
Recruiting Trial Workers Amidst Growing Complexity
Economic challenges combined with increased responsibility for clinical trial workers has shifted talent recruitment.
Tokenization: Practical Applications in Clinical and Real-World Research
Webinar Date/Time: Tuesday, December 13, 2022 at 10am ET | 3pm GMT | 4pm CET
Methods to Recruit Healthcare Providers for Virtual Advisory Boards in Drug Development
Tufts CSDD study addresses barriers in recruitment.
Mobilizing and Maintaining Clinical Trials in Midst of War
Ukraine invasion tests the resiliency and quick action of CROs and sponsors.
The Implications of Inflation for Drug Development
Experts gauge threat level for global trials amid staffing and funding issues.
Leveraging Data Insights to Address the Perils of Linear Practices in Site Identification and Activation
Phesi and Tufts CSDD share results from research on operating practices that can be improved.
A Biosafety Perspective on Operational Challenges in Cell and Gene Therapy Studies
The benefits of working with an institutional biosafety committee in CGT research.
What the Future of Study Review Processes Should Look Like
Insights from Bayer’s study review process showcases importance of incorporating feedback from a wider audience of stakeholders.
Make Your Clinical Trial a Priority in a Busy Landscape
A more crowded space is presenting new challenges for stakeholders that must be addressed to improve efficiency.
Build Relationships with HCPs to Reach Potential Clinical Trial Patients
Increased outreach is necessary to combat poor recruitment and large focus on patients near study centers.
Game Changer: Transformative Decentralized Clinical Trials Emerge in Latin America
Regional factors impact direct-to-patient modalities and bring the benefits of DCTs to life.