The Fountain Group

Project Coordinator III (Clinical Technology) for a prominent client of ours.. Full-Time, Monday – Friday, normal work hours, potential for hybrid work schedule.. Seeking a highly motivated and detail-oriented Clinical Technology Program Coordinator.. Bachelor’s Degree in a relevant field (Biology, Clinical Research, Health Sciences, etc.). Strong understanding of clinical research protocols and regulatory requirements.

project coordinator

The Fountain Group is a national staffing firm and we are currently seeking a ­­­­­­­­Project Coordinator III (Clinical Technology) for a prominent client of ours. This position is in ­Irvine, CA 92612. Details for the position are as follows: Job Description:<ul><li>$42 - $45/hour based on previous experience. </li><li>Full-Time, Monday – Friday, normal work hours, potential for hybrid work schedule. </li><li>Seeking a highly motivated and detail-oriented Clinical Technology Program Coordinator. </li><li>This role is crucial in bridging the gap between Clinical study teams and our internal Clinical Technology (ClinTech) stakeholders, focusing primarily on the integration and effective use of ClinTech digital services. </li><li>Serve as the primary contact between study teams and the ClinTech team, fostering clear communication and collaboration.</li><li>Engage in study meetings to fully grasp protocols, objectives, timelines, and requirements.</li><li>Ensure the creation and prompt delivery of specific study materials and outputs.</li><li>Offer extensive support and training on the proprietary platform, guaranteeing optimal setup and use by study teams.</li><li>Regularly contribute to the creation and refinement of clinical study materials, like instructions and training documents.</li><li>Acquire and sustain in-depth knowledge of the platform, staying informed on its capabilities and updates.</li><li>Assist study teams in leveraging the platform fully by exploring its additional features and modules.</li><li>Collect and relay user feedback and feature requests to the development team to facilitate platform enhancements.</li><li>Monitor digital services activities to ensure their alignment with study goals and outcomes.</li><li>Oversee the progress of digital services ensuring their effective integration with the platform for study success.</li><li>Regularly report on study and platform-related progress, challenges, and achievements to both study teams and management, ensuring transparency and facilitating informed decision-making.</li></ul> Qualifications:<ul><li>Bachelor’s Degree in a relevant field (Biology, Clinical Research, Health Sciences, etc.)</li><li>Experience in clinical study coordination or management, particularly in a technology-driven environment. </li><li>Experience working in life sciences. </li><li>Strong understanding of clinical research protocols and regulatory requirements. </li><li>Excellent communication and collaboration skills, with the ability to act as a liaison between various teams. </li><li>Proficiency in digital tools and platforms, with a willingness to become an expert user of the proprietary platform. </li><li>Detail-oriented with strong organizational and project management skills.</li></ul>

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