eClinical 101

If a technology tool can empower a clinical trial site manager to accomplish their job more efficiently, effectively and economically, it’s a tool well worth considering. eClinical is just such a resource. The technology provides site managers with a suite of solutions that streamline data collection, patient consent, compliance, information sharing and much more.  What […]

Enhance Your Patients’ Trial Experience

Too often, clinical trial managers focus so much on the recruitment, scheduling, administration, expenses, results, and other details of a trial that they forget one very important element: the patients. The people participating in your trials aren’t just another bit of data to enter in your CTMS—they’re human beings, and their experience interacting with your […]

Increasing Clinical Trial Patient Diversity

Attaining a diverse trial patient population is crucial to your site’s success. It is possible the treatments your trial is putting to the test may affect people from varying racial, ethnic, and age groups differently. However, your sponsors won’t know if that’s the case unless your trial team is able to reach, recruit and retain […]

Stand Out During Site Selection

Site selection is a critical piece of your research business’ success. Given increased competition amongst research sites, sponsors are in control and your job is to maximize opportunities for them to select your team. Above all, sponsors want a site partner that can offer efficiency and effectiveness. This includes meeting (and exceeding) enrollment goals, demonstrated […]

Four Critical CT Data Points

Efficiency is key in clinical trials, and one way to derail those streamlined trials is to waste time on non-critical data points. If a site and sponsor expend energy gathering information that isn’t vital, they have less time to discern and apply the metrics that matter. A few of those important data points include: Pinpointing […]

Simplifying Trial Management

Clinical trials allow innovators to obtain reproducible, accurate results and make significant impacts on people’s lives. Reviewing processes with an eye toward simplification is a critical step to managing effective and efficient trials. Simplification reduces inertia, resource waste, and error. It also helps propel the underlying goals of the trial: advancing innovations and caring for […]

Tackling Compliance Bottlenecks

How clinical research sites handle compliance issues is perhaps the most critical aspect of their profession. Understanding and mitigating compliance risks not only ensure the highest level of patient safety and care, but are also necessary for all partnerships, funding and government oversight elements of a research business. With patient data security and safety concerns […]

Demonstrating Your Value to Sponsors

Understanding what sponsors want from their relationships with both CTOs and specific sites boils down to one thing: reducing risk. Enrolling and retaining patients is a long process that’s also the most critical component of a successful trial. Sponsors want to be ensured that performance is being monitored and reported upon accurately so they can […]

Text Me: Using Text Messaging to Increase Patient Recruitment & Engagement

Patient recruitment and retention are two of the most important elements of successful clinical trials. Increasing results in these areas is a constant goal for almost any research business and understanding the best ways to achieve them are critical for success. Clinical trial teams have a number of strategies and tools to increase patient interest, […]

6 Questions to Ask When Trying to Tackle Inefficiencies in Your Research Business

There are likely a number of inefficient processes across your research organization. Developing a list of problem areas is the first step to mitigating these inefficiencies. Here are six questions that will help you and your team establish a comprehensive and actionable list of areas for improvement: Is my team able to track recruitment, enrollment, […]