Resources

Author: Meghan Hosely

Meghan Hosely

Meghan is the Marketing Content Writer for Forte, and is an active contributor to Forte’s educational resources, including webinars, blog articles, eBooks and more.

Social Media Marketing for Patient Recruitment

With recruitment challenges on the rise for sites, consider finding potential participants on social media.

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Performing Protocol Feasibility Assessments to Enhance Clinical Trials

Protocol Feasibilities are designed to help clinical research staff determine the possibility of conducting a study. Here’s how to seamlessly work an assessment in before accepting your next clinical trial.

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Strategies for Retaining and Motivating Your Employees

Over the last 10 years, turnover at CROs was around 20%. Learn how extrinsic and intrinsic motivation could help you retain your employees.

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Unpacking the Benefits and Drawbacks to eConsent

With electronic processes dominating systems, electronic consent is starting to make its way onto the scene. Check out the benefits and drawbacks to the alternative consent process.

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Maximizing Recruitment Potential for Research Studies

Chanel Mansfield and Neva Garner, both of the University of Colorado Denver Anschutz Medical Campus, presented at the 2019 Fall Onsemble Conference on lessons learned during the recruitment process.

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Onsemble Community Members Work to Transform Clinical Research with a Site-Centric Approach

We are about halfway through the 2019 Fall Onsemble Conference, which has been full of conversations and collaborations our customers will take back to their respective institutions. Here’s a sneak peek of what we’ve been learning.

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How to Recruit Patients for Clinical Trials

A big challenge for any clinical research staff is obtaining participants for their trial. Explore different methods and strategies to recruit participants for your current and upcoming trials.

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Billing Compliance Basics: What Clinical Researchers Should Know

Billing compliance makes sure all services in a trial are paid for by helping to reduce double billing and preventing billing for services that are not covered by the trial or are not medically necessary for the participant.

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

Conducting informed consent is more than making sure your participants understand the protocol. Learn more about when, why and how it’s obtained continuously throughout a trial.

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Beginner’s Guide to Risk-Based Monitoring

In clinical research, there are many different data points to track and monitor as the trial moves from phase to phase. Learn more about risk-based monitoring and how it fits in with clinical trials.

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