Dominique Fuller, CCRA

As the founder and owner of DM Us 4 Home Improvement, I manage all aspects of daily operations for a growing residential and commercial painting business. My responsibilities include project planning, scheduling, budgeting, team management, and client communication. I’ve built the business from the ground up—developing systems for lead generation, sales, and service delivery while ensuring quality control across every job. Through this hands-on leadership, I’ve gained valuable experience in negotiation, process improvement, team coordination, and building scalable workflows under pressure.

Since April 2021, I have been managing a portfolio of four residential properties, one of which is listed on both Airbnb and VRBO. I handle all aspects of property management, including guest communication, maintenance coordination, and financial oversight, to ensure a seamless experience and maximize occupancy. This role has honed my skills in real estate investment, short-term rental management, and strategic decision-making to sustain and grow property value.

Responsible for working with clients and assuring the provision of clinical trial supplies by interpreting protocol specifications and developing, integrating, and implementing materials and procedures that meet study requirements. Collaborate with cross-functional teams to plan, implement, and manage clinical trials, ensuring adherence to timelines and budgets. Ensure all clinical activities comply with relevant regulations and guidelines, including FDA, EMA, and ICH-GCP standards. Oversee the selection and management of external vendors, including CROs, laboratories, and other service providers, ensuring high-quality deliverables. Assist in the identification, initiation, and monitoring of clinical trial sites, fostering strong relationships with site staff to facilitate effective study conduct. Identify potential risks to project timelines and quality, and develop mitigation strategies to address these challenges proactively. Maintain comprehensive and accurate project documentation, prepare progress reports, and communicate updates to stakeholders. Provide training and guidance to clinical research associates and site staff on study protocols and procedures. Participate in process improvement initiatives to enhance the efficiency and effectiveness of clinical operations.

In this role at HAYS RECRUITING (IQVIA), I was responsible for performing comprehensive site monitoring activities, including site selection, initiation, and close-out. I effectively developed subject recruitment plans and maintained strong communication with assigned sites. My tenure here was marked by a dedication to enhancing the quality and integrity of site practices, ensuring the smooth progression of clinical trials.

During my tenure at HAYS RECRUITING (Biorasi), I specialized in optimizing clinical trial processes, including site management and monitoring. I focused on fostering effective relationships with site staff and ensuring compliance with trial protocols. My role involved strategic planning, oversight of crucial trial components, and ensuring data accuracy, contributing to the overall success of the clinical studies.

At REAL STAFFING (Thermo Fisher Scientific), I held the role of Senior CRA III, overseeing complex clinical trials with a focus on ensuring protocol compliance, site performance, and data integrity. My responsibilities included extensive site monitoring, establishing efficient communication channels with clinical sites, and managing critical issues with actionable solutions. I played a pivotal role in maintaining high standards of data quality and regulatory adherence, contributing significantly to the success of clinical research initiatives.

At LABCORP, my role as a Senior CRA II involved managing and monitoring various aspects of clinical research trials. I ensured protocol adherence, conducted detailed site assessments, and managed investigational products. My focus was on optimizing trial processes, improving data collection, and ensuring patient safety, thereby contributing significantly to the successful execution of clinical trials.- Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans and trip report review as assigned. - Independently perform CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management.

In my role at ICON GPHS, I was integral in assisting with project coordination, planning, and logistics, including the oversight of budgets and timelines. My responsibilities included providing daily oversight of Clinical Research Associates and acting as a communication link between the sponsor and the research team, ensuring effective project execution.

At SYNEOS HEALTH, as a CRA II, I was responsible for monitoring interventional clinical trials, ensuring adherence to Good Clinical Practice and study procedures. My role involved site management, remote monitoring using clinical systems, and conducting on-site monitoring activities, aligning with risk-based monitoring modules when required.