Bio-Optronics is the creator of Clinical Conductor (CC CTMS), known for generating significant savings with its robust finance capabilities, it is also the leading CTMS for executing collaboratively across multiple clinical trials and sites, including enabling remote workflows. Used by more research sites around the world than any other CTMS, Clinical Conductor is currently managing over 40,000 studies, including a significant percentage of the world’s COVID-19 clinical trials.
CC CTMS is part of the CCTrialSuite, a comprehensive set of integrated, patient-centric clinical research management products that together streamline research operations while maintaining a high degree of compliance. Complementing Clinical Conductor in the suite are several remote workflow enabling solutions. CCPay offers sites the unprecedented ability to both control finances and improve patient satisfaction with real-time payment reimbursements using secure pre-paid payment cards, all controlled remotely from CC CTMS dashboards. While CCText, the only fully CTMS-imbedded, conversational 2-way text messaging solution, has demonstrated clear results with increased patient recruitment, engagement and retention. An expanding set of remote workflow capable solutions include Part 11 compliant CCeReg document management, remote monitoring enabled CCeSource data capture, mobile friendly CCeConsent, and easy to engage remote visits using the HIPAA compliant CCVideo solutions from a single SaaS supplier, Bio-Optronics.
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Scientific teams require highly specialized skill sets that are in higher demand than ever before. The talent skills gap is real, and regulations across a wide range of scientific settings require an expert workforce.
Since 2009, Medix’s Scientific Division has connected scientific teams with highly skilled and sought after talent. As the numbers of registered clinical trials in America rose rapidly in the following years, Medix Clinical Research was founded in 2013 to service sites, sponsors and CROs of all shapes and sizes. In 2015, Medix Clinical Research introduced client consulting, bringing a more personalized approach to the site experience by providing expert guidance.
Today, our team supports scientific clients with staffing, workforce solutions and consulting in Clinical Research Sites, Pharmaceutical/Biotechnology, Medical Device and Food & Beverage
The increased demand for clinical research trials has created talent imbalances for sites, leading to staff dissatisfaction, financial instability and, ultimately, lower quality trials. Through our best-in-class recruitment services and proprietary behavioral assessment, we will deliver talent who match your needed hard skills, soft skills and cultural fit. Every site’s needs are different, so whether it’s operational or compliance based, our in-house clinical research staff is dedicated to help your site build a sustainable research program.
Medix Clinical Research offers a full range of staffing, consulting and workforce solutions for clinical research sites, including:
Site Operations
Finance (Budget and Contracting, Revenue Collection Cycle)
Compliance
Recruitment and Retention of Talented Staff
Clinical Research Boot Camp, powered by ACRP
For more information, please visit www.medixteam.com, or contact us at 1-866-44-MEDIX.
Total Clinical Trial Management (TCTM) is a full service CRO created on the founding principle that relationships between research sites and the CRO is a critical element in ensuring successful study completion. TCTM’s proprietary TotalTouch Site Advantage process has proven to dramatically increase study timelines and deliver results.
Areas of focus include pain, orthopedic injury, dermatology and generic and OTC studies. TCTM boasts an in-house patient recruitment team with a track record of successful enrollment strategy and tactical planning.
Whether your priority is networking with sponsors and CRO attendees or learning best practices built for research sites, the Summit will provide a unique experience for your business.
For the last 16 years, the Global Site Solutions Summit has been committed to being “the site’s meeting.” The Summit provides a unique hub where sites, sponsors, CRO executives and regulators come together and share best practices, build their businesses, and develop new partnerships through debates, ideation sessions, workshops and focus groups.
SCRS is confident that by increasing site sustainability, all life science stakeholders will realize greater efficiency and profitability, and successfully meet our ultimate commitment to bring safe medical treatments to patients faster. The Global Summit will deliver the high-quality education, training, and best practices that attendees have come to expect.
BRANY was founded by the country’s leading academic medical centers in 1998, and has a stellar track record of working with community and academic hospitals and established investigators. BRANY understands the importance of high quality human subject research. In today’s increasingly complex study environment, we excel in helping IRB’s and hospitals continue to provide their patients with high quality clinical research. BRANY offers personalized customer service and project management, as well as ongoing communication through our quarterly newsletter and regular email updates
