Clinical Studies Coordinator - Irvine

We are seeking a highly experienced Clinical Studies Coordinator to lead and execute end-to-end clinical studies supporting FDA submissions (510(k)), pilot and feasibility studies, post-market clinical follow-up, and real-world evidence generation. · ...

+The Study Regulatory Coordinator leads regulatory processes across multiple studies in accordance with appropriate regulations and study specific protocols/plans.+ · +Essential Functions & Responsibilities:Manages regulatory activities for all stages of clinical trials. · Mainta ...

The Study Regulatory Coordinator leads regulatory processes across multiple studies of different therapeutic areas and phases. · ...

We warmly welcome you to consider joining the Titan Community where minds expand and opportunities flourish. · ...

It is an exciting time to join Cal State Fullerton as we are an in demand comprehensive University that is driven to shape the future of education and foster a vibrant community of diverse students... · ...

It is an exciting time to join Cal State Fullerton as we are an in demand comprehensive University that is driven to shape the future of education and foster a vibrant community of diverse students, faculty, staff, and administrators who uphold values of inclusive excellence, fre ...

Performs various activities within the Clinical Sciences department in support of clinical trials and projects. · Bachelor's degree or higher from an accredited institution; preferred degree in sciences. · Microsoft Office products – Word, Excel, PowerPoint, Project. · ...

The Regulatory Coordinator is responsible for managing and maintaining clinical study regulatory documentation in full compliance with IRB sponsor and FDA requirements ensuring all records remain inspection-ready at all times. · This role supports study startup maintenance and cl ...

Kelly Science and Clinical FSP is currently seeking an Operations Coordinator for a long-term engagement in Irvine CA with one of our Global Pharmaceutical clients. · ...

Irvine Clinical Research is seeking a Clinical Scientist to work on prescreening and screening potential candidates for outpatient Phase II/III clinical trials in Neurology and Psychiatry. · ...

We are the people behind the people who keep saving lives. · Cordis is just the place for you if you love a challenge and are ready to have a direct, transformative and positive impact on the lives of millions. · ...

When you join the team at Cordis, you become part of an inspiring mission to save lives... · ...

The Research Operations Associate works closely with discovery development and project-planning teams at an AI-powered TechBioPharma company. · Bachelor's degree in biological sciences or related field. · Two to three years of research experience in a biological sciences field. · ...

Kelly Science and Clinical FSP is currently seeking a Clinical Study Administrator for a long-term engagement in Irvine, CA with one of our Global Medical Device clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and b ...

Kelly Science and Clinical FSP is currently seeking a Clinical Study Administrator for a long-term engagement in Irvine, CA with one of our Global Medical Device clients. This role is full-time and is offering full benefit options. · ...

Kelly Science and Clinical FSP seek a Clinical Study Administrator for a long-term engagement in Irvine CA with one of their Global Medical Device clients. · ...

Brandywine Homes seeks a Project Manager to manage 4-5 projects simultaneously. · ...

+Job Summary · Clinical scientist will work on prescreening and screening potential candidates for outpatient Phase II/III clinical trials in Neurology and Psychiatry. · +ResponsibilitiesAssess potential and returning study participants using clinical judgement as well as psychol ...

The position will require working effectively on a team and contributing to segments of larger projects, multi-disciplinary coordination, monitoring scope schedule and budget ensuring client satisfaction. · ...

The primary responsibility of the Clinical Data clinical data analyst is to support CDM study start-up activities. · Develop database specifications · Author and execute test scripts · ...