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Meghan Hosely

Marketing Content Manager, Advarra

Meghan Hosely is the Marketing Content Manager at Advarra, creating content across the business. In her role, Hosely provides educational content for Advarra’s website, such as blogs, eBooks, white papers, and more. Hosely has been with Advarra since 2019, working with subject matter experts to produce relevant and timely content for the Advarra website.

Latest Posts by Meghan Hosely

Digital Health, COVID-19, and the Evolution of Clinical Trials

The COVID-19 pandemic has driven transformative changes across industries, and clinical research is no...

Informed Consent: When, Why, and How It’s Obtained

Informed consent isn’t just a formality—it’s an evolving process that safeguards participant autonomy and enhances...

Tips for Writing Effective Edit Checks in eCRFs

Edit checks are a great mechanism to improve data quality within an electronic data capture...

The Key to Increasing Diversity in Decentralized Trials

Historically, decentralized clinical trials (DCTs) were heralded as the future of patient-centered research. But how...

Increasing Diversity, Equity, and Access in Clinical Research: A Case Study

In the evolving landscape of clinical research, increasing diversity, equity, and access has become...

Connecting Patient Centricity and eConsent Together

Patient-centric trial design, combined with eConsent, fosters better communication, comprehension, and retention, ensuring a smoother,...

The Role of Data in Optimizing Clinical Trials: Key Insights for Sites and Sponsors

In the fast-evolving landscape of clinical research, data collection and performance metrics are indispensable...

Different Players Involved in Reviewing Clinical Research

Clinical trials play a critical role in the development of new drugs and devices,...

Building Patient-centricity in Clinical Trials: Lessons and Future Directions

The concept of patient centricity is a recurring theme in clinical research, but the...

Navigating the Complexities of Clinical Trial Budgeting and Billing Compliance

Clinical trial activation involves a host of tasks, from institutional review board (IRB) tasks...

The Rise of Gene Therapy: A New Era in Medicine

Gene therapy is rapidly transforming from an experimental treatment into a cornerstone of modern...

Enhancing Diversity, Equity, and Inclusion in Cancer Research: Overcoming Challenges in Clinical Trials

Diversity, equity, and inclusion (DEI) are critical pillars in the evolving landscape of cancer...

Digital Health, COVID-19, and the Evolution of Clinical Trials

The COVID-19 pandemic has driven transformative changes across industries, and clinical research is no...

Informed Consent: When, Why, and How It’s Obtained

Informed consent isn’t just a formality—it’s an evolving process that safeguards participant autonomy and enhances...

Tips for Writing Effective Edit Checks in eCRFs

Edit checks are a great mechanism to improve data quality within an electronic data capture...

The Key to Increasing Diversity in Decentralized Trials

Historically, decentralized clinical trials (DCTs) were heralded as the future of patient-centered research. But how...

Increasing Diversity, Equity, and Access in Clinical Research: A Case Study

In the evolving landscape of clinical research, increasing diversity, equity, and access has become...

Connecting Patient Centricity and eConsent Together

Patient-centric trial design, combined with eConsent, fosters better communication, comprehension, and retention, ensuring a smoother,...

The Role of Data in Optimizing Clinical Trials: Key Insights for Sites and Sponsors

In the fast-evolving landscape of clinical research, data collection and performance metrics are indispensable...

Different Players Involved in Reviewing Clinical Research

Clinical trials play a critical role in the development of new drugs and devices,...

Building Patient-centricity in Clinical Trials: Lessons and Future Directions

The concept of patient centricity is a recurring theme in clinical research, but the...

Navigating the Complexities of Clinical Trial Budgeting and Billing Compliance

Clinical trial activation involves a host of tasks, from institutional review board (IRB) tasks...

The Rise of Gene Therapy: A New Era in Medicine

Gene therapy is rapidly transforming from an experimental treatment into a cornerstone of modern...

Enhancing Diversity, Equity, and Inclusion in Cancer Research: Overcoming Challenges in Clinical Trials

Diversity, equity, and inclusion (DEI) are critical pillars in the evolving landscape of cancer...

Digital Health, COVID-19, and the Evolution of Clinical Trials

The COVID-19 pandemic has driven transformative changes across industries, and clinical research is no...

Informed Consent: When, Why, and How It’s Obtained

Informed consent isn’t just a formality—it’s an evolving process that safeguards participant autonomy and enhances...

Tips for Writing Effective Edit Checks in eCRFs

Edit checks are a great mechanism to improve data quality within an electronic data capture...

Sponsors/CROs
Research Sites
Offerings
Resources
About
Careers at Advarra
Logins
Contact
Search

Sponsors/CROs
Research Sites
Offerings
Resources
About
Careers at Advarra
Logins
Contact
Search

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