Christopher Reed
Technical Director at Princeton Consumer Research
Based in Ruskin, United States
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Seniority
Director
Department
Information Technology
Location
Ruskin
Industry
Research Services
Company size
77
Contact information
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c•••••••@princetonconsumer.com
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Background
About Christopher Reed
Mission Statement: I am dedicated to advancing clinical research through innovative solutions, fostering collaboration, and driving continuous improvement to enhance patient outcomes and streamline research processes. As an accomplished Technical Director with a robust background in clinical research management, I specialize in developing and implementing efficient data entry systems and clinical research instrumentation. My career is marked by a commitment to excellence and continuous improvement, demonstrated through my ability to reorganize teams to boost productivity and pioneer training curricula that enhance interdepartmental collaboration and staff competencies. With extensive experience overseeing multi-site clinical operations, I excel in maintaining compliance with industry standards and regulatory requirements. My expertise spans across various medical disciplines, including oncology, gastroenterology, nephrology, and endocrinology, ensuring meticulous attention to detail in all aspects of clinical trial management. Key Accomplishments: Spearheaded the development of new testing methods and maintenance protocols for clinical instrumentation. Led initiatives to enhance team performance and efficiency through comprehensive training programs. Successfully managed clinical trials across North America and Europe, consistently meeting client needs and expectations. Implemented process improvements that resulted in increased efficiency in data collection and entry. Reorganized clinical operations teams, boosting productivity and team cohesion. Played a pivotal role in customer service initiatives, ensuring client satisfaction and adherence to clinical standards. Skills: Clinical Research Management Training Curriculum Development Medical Devices Phases I-IV Clinical Trials Electronic Medical Records (EMR) Multi-site Clinical Operations Process Development Regulatory Compliance (FDA, GCP, ICH) Institutional Review Board (IRB) Software: Microsoft 365, CTMS (Clinical Conductor, RealTime, Advarra Suite, EHR, and EDC Systems I am passionate about fostering a culture of learning and collaboration, and I am dedicated to driving innovation in clinical research. Let's connect and explore how my skills and experience can contribute to your organization's success.
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