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Sites, Sponsors, CROs: Discover the solutions your clinical research teams need with SCRS.


Bio-Optronics, creator of Clinical Conductor CTMS, is one of the fastest growing healthcare workflow optimization software and services companies, dedicated to positively impacting the lives of patients and providers. Recognized for providing the comprehensive functionality required to recruit effectively, optimize billing, maintain research compliance, extract actionable business insight and maximize profitability, Clinical Conductor is also integrated with the major clinical systems, eliminating double entry issues. Used by more research sites than any other system, Clinical Conductor CTMS simplifies and standardizes complex clinical research processes and finances for professionals managing and conducting clinical trials, helping our users run the world’s best research and increasing the chances of being the chosen site for each new opportunity.

Click here for free access to The Ultimate Guide to Clinical Trial Software!

Also visit www.bio-optronics.com or follow @BioOptronics on Twitter or LinkedIn 


  • Clinical Conductor CTMS

    Clinical Conductor CTMS is the only clinical trial management system with strong financial and compliance capabilities that is designed to accommodate the unique needs of your organization across multiple sites and countries. Run the world’s best research.

    More Information » bit.ly/2Tkjj8i

    Clinical Conductor CTMS


QPS Miami Research Case Study
January 10, 2018 11:44am


CRS Case Study
January 10, 2018 11:44am


Integration with Complion
January 10, 2018 11:47am

News: Bio-Optronics 
  • Improve Trial Funnel and ROI Results with eConsent March 18, 2019 12:29pm

    Consent and patient comprehension are two of the key pillars for successful trial management. And while this technology isn’t necessarily new, it is experiencing increased adoption by both CTOs and regulators across the globe. A recent study showed that 20% of trials are expected to use eConsent in the next three years and 25% of […]
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  • Create a Successful Billing Compliance Program This Year February 25, 2019 8:41am

    With the start of a new fiscal year, there are important steps you need to take to build a successful clinical trial billing compliance program. The following information will help you develop procedures for handling any reimbursement issues that arise. Evaluate Your Current State When developing an effective compliance program, you’ll need to establish a […]
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  • Optimize Your Research Program Through Structure and Staffing February 10, 2019 8:57am

    The benefits of having a research program within your organization are both direct and indirect. The obvious direct benefit is the financial value created by providing a revenue stream, attracting new patients, and increasing ancillary services. Indirectly, having a research program not only enhances the site’s visibility but also increases market share and improves community […]
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  • Selling Your Site: Business Development in a Changing Industry February 5, 2019 8:55am

    The pharmaceutical industry is constantly changing, especially over the past few years. Research and development costs are growing exponentially, while mergers and acquisitions are being leveraged to increase revenue, decrease costs, gain influence, and eliminate competition. As sponsors move from high-volume/low-margin business models to low-volume/high-margin models, there is increased competition among sites for fewer research […]
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  • Avoiding Common Pitfalls in the Beginning Phases of IITs January 30, 2019 9:50am

    Establishing your site as an IIT powerhouse can be an incredibly lucrative way for the administration to show support for their PIs’ initiatives and interests. Investigator-Initiated Trials (IITs) have seen an increased interest within the clinical research field. Both industry sponsors and investigators are recognizing these undertakings as important investments and are collaborating to maximize […]
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  • 3 Hidden Benefits of Documented Quality Control Practices January 26, 2019 11:15am

    Everyone understands how important quality control is to clinical trials. Without standard operating procedures, researchers cannot ensure site staff perform tasks consistently—or even correctly. And yet, The Global Journal for Clinical Research Sites states that it’s common for sites to not document their internal quality control practices or SOPs. Sites overlook this step for many […]
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  • Bio-Optronics
    1890 South Winton Road
    Rochester, New York 14618
    United States
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  • Last UpdatedMarch 23, 2019 8:06am EDT



  • Michael Bonavilla
    Michael Bonavilla

    Director, Business Development
    Bio-Optronics, Inc.
    Charlotte, South Carolina

  • Katie Gaiek
    Katie Gaiek

    Sales Executive
    Rochester, New York