Timothy Richardson Email & Phone Number

Cumming, Ga, Us

Raritan, Nj, Us

Suwanee, Georgia, Us

Greenville, South Carolina, Us

Geneva, Switzerland, Ch

Watford, Hertfordshire, Gb

Horsham, Pa, Us

Provides leadership and clinical research expertise to efficiently manage the clinical operations and quality within the CNS sitesOversight of multiple locations and works to ensure operational successProfit and Loss accountability for their designated area of responsibility Responsible for oversight, training and recruitment of employeesEnsure quality care to patientsEnsure quality data at sitesGenerate study status reports, data tables, presentations and correspondenceCoordinate the purchase, receipt, inventory and distribution of study equipment Assist with development and distribution of study communication Oversight and direction of recruitment at the sites

Horsham, Pa, Us

• Provide leadership and oversight over the daily clinical research activities according to the organizations SOPs, GCP and FDA/ICH guidelines. • Overall accountability and responsibility of the site’s P&L. • Provide guidance and training to the clinical research coordinators and assistants to ensure efficient and high quality site operations. • Proactively participate in quality reviews and works with the Region Director, Director of Clinical Operations and/or the VP of Operations to implement the appropriate corrective actions. • Provide the site staff with expertise and guidance on recruitment and enrollment of the clinical trials to ensure site(s) profitability. • Function as the organization’s liaison to the physician and physician practice to ensure the appropriate Investigator oversight is maintained at all sites responsible for. • Accountability for the site’s financial performance and continually seeks out improvements to enhance the overall business. • Provide training and mentoring to site staff and the Investigator, and serves as the onsite leader and exemplifies the core values of the organization. • Perform clinical tasks (i.e. phlebotomy, EKGs, vital signs, etc.) and fully function as a clinical research coordinator as necessary

Site Management Organization providing clinical trials resources to physicians and medical groups. We specialize in study start up, clinical trial administration, and providing customized research solutions to clinical trial sites. Trinity can also work with sponsor companies in the areas of site selection and monitoring of protocols.

Quincy, Massachusetts, Us

Responsible for developing, implementing and overseeing processes that support the operational aspects of activating a study site and clinical trials at GuideStar contracted sites. Coordinate and oversee trial selection, financial analysis and regulatory management of clinical trials. Responsible for providing functional direction to the research staff at established sites assigned to the various clinical programs by setting operational standards, providing staffing continuity, and monitoring staff progress. Emphasize site enrollment, data quality, and timely submission of data to sponsors.GuideStar Clinical Trials Management works with hospitals, health systems and physician practices around the country to build, manage and support clinical researchprograms. Our expert team provides on-site program management, regulatory processing, strategic marketing consultation, a pipeline of clinical trials, budget development and negotiation, contract negotiation and technology tools to track clinical trial protocols and finances. From behind the scenes, GuideStar aids our partner facilities provide their community with the latest therapies, drugs and devices and be on the forefront of medical breakthroughs.

Manage and direct sleep laboratories in Georgia and South Carolina; responsible for overall operations and quality assurance in sleep labs; consult with the medical director to ensure effective patient treatment; analyze polysomnographic recordings; train and educate staff.

M.S., Health Administration

B.S., Biology

Education record