Authors


Bart Dewolf

Latest:

Collaborative Strategies for Technology Integration in Clinical Studies

Addressing data integrity and compliance concerns.


Robert Paarlberg

Latest:

Clinical Trial Disclosure and Data Transparency: Obligation or Opportunity?

Implementing disclosure and data transparency policies and procedures represents an opportunity for sponsors, rather than an obligation.


Kenny Kong

Latest:

Focus on Fundamentals for Better Collaboration Across Research Sites and Sponsors

Improving the site-sponsor relationship can get trials off on the right foot and on a path for success.



Iddo Peleg

Latest:

Can Clinical Trials Overcome Their Staffing Problem?

The current lack of clinical trial professionals is a serious concern that's compromising the ability to conduct high-quality clinical trials, but it's not irreversible.


Rhonda Henry

Latest:

The Two Guiding Principles of Optimal Trial Delivery

Trust-based relationships form the foundation for successful trial management.


Dan Hydes

Latest:

Innovations in Data Capture Transforming Trial Delivery

Advances in technology open door for improved EHR to EDC transfer process.


Annick de Bruin

Latest:

Awareness of Clinical Research Increases Among Underrepresented Groups

Latest CISCRP study provides insight on proactive outreach.


Caroline Smith

Latest:

Rebadging Gains Momentum Amidst COVID

Capacity management and stability offer value for clients, their employees and FSP vendors.


Emily Hardy

Latest:

The Future of Clinical Trials: Turning Data Chaos into Trial Intelligence

Poll taken by leading biotech executives in clinical development addresses state of data quality and management.


Swathi Ramesh

Latest:

Introducing PALADIN

First-of-its-kind consortium dedicated to accelerating new medicines development through optimizing patient advocacy group—industry collaboration.


Melanie Anderson

Latest:

Opportunities for Improving Clinical Decisions with Patient Centric Remote Blood Sampling Approaches

This article sets out a vision of adopting convenient alternative blood sampling approaches that places the needs of the patient at the center and enables active monitoring, before the onset of clinical events, leading to improved healthcare.


Aman Thukral and Sanjay Bhardwaj

Latest:

Revolutionizing Clinical Data Management: The Leap from Deterministic to AI-Powered Stochastic Methods

Leveraging artificial intelligence-powered stochastic methods for clinical data review represents a significant leap beyond traditional approaches.


Cytel

Latest:

Empowered Trial Selection with Weighting and Prioritization Tools

Thursday, September 30, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Give yourself a competitive edge by learning how the world’s leading designer of innovative clinical trials can help you integrate elements of economic theory to your clinical trial design. Optimize sample size, speed, and power by exploring a broader array of designs and quickly identifying those that meet your objectives.


Helen Yeardley

Latest:

The CRA of the Future: From ‘Road Warrior’ to Site ‘Owner’

Adjusting to the changing dynamics of the clinical research associate role.


Hanna Wide

Latest:

The Rise of Gene Therapy: Advanced Regulatory, Site, and Enrollment Considerations

Developing new pathways to overcome study-related challenges is key to realizing the promise of the latest gene therapies.


Jamie Harper, MHA, CCRP

Latest:

Diversity in Clinical Trials: Strategies and Challenges

Why weighing all of the ‘DE&I’ components is critical at site and sponsor levels.


Aubrey Llanes

Latest:

Thoughtful Design in eCOA Development: Part 2

To derive the greatest benefits from eCOA technology, several elements must work together to create a strong foundation for sponsor success.


Radha Krishnan

Latest:

Managing Biospecimens in Cell and Gene Therapy Trials

Pursuing new tools and capabilities in sample logistics, storage, and data analysis.


Zachary Smith

Latest:

Benchmarking the Investigative Site Qualification Process

Insights identify opportunities to optimize sponsor, CRO, and site collaborations.


Jill Sommerville

Latest:

Unleashing Their Potential: The Evolving Landscape of DHTs

Key considerations in deploying fit-for-purpose digital health technologies in drug development.


Mary New

Latest:

Harnessing Patient-Centered Science to Improve Health Outcomes and Commercial Pharma Success

Good scientific principles and practices are essential for maintaining quality data that patients can benefit from.


Lee Andrews II

Latest:

Scaling eSource-Enabled Clinical Trials: Hospital Perspectives

The challenges, opportunities, and strategic outlook for oncology research centers.


Bill Meisle

Latest:

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.


Samantha S. Williams-Gray

Latest:

Clinical Trials and Trust

Understanding the role of social determinants on clinical trial participation and trust.


Preet Singh

Latest:

Future of Clinical Trial Documentation Management: eTMF Integrated with Blockchain

eTMF-blockchain technology offers a myriad of application benefits to data quality and integrity while ensuring compliance to ethical standards.


Guy Rachmuth, PhD

Latest:

Integration of Point-of-Care Devices in Clinical Trials

A look at the future of clinical trial laboratory testing amid the emerging use of new devices at the point of care.


Phil Mounteney

Latest:

COVID-19 Five Years Later: The Impact on Drug Discovery

COVID-19 not only advanced scientific boundaries, but also transformed research methodologies and accelerated adaptive clinical trial design.


Jasmina Jankicevic, MD

Latest:

Navigating the New World of Dermatology Trials

How partnering with a CRO that has experience in both dermatology and innovative trial approaches can help sponsors differentiate their studies and facilitate recruitment.


Jiangyuan Luo

Latest:

Towards Data-Driven Clinical Trial Planning and Strategy

Optimizing feasibility through increased data collection.

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