Senior Clinical Study Manager - Irvine

Selution, in partnership with Cordis, · specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creat ...

The Senior Clinical Study Manager (Sr. CSM) will provide leadership, direction, and oversight for a complex, multi-center patient registry within the MedAlliance LLC / Cordis SelutionSLR portfolio. · The Sr. CSM serves as a key point of contact for global study/registry stakehold ...

+ Lead planning initiation management assigned global patient registries duties across multiple regions Develop maintain project plans risk management strategies timelines following timely escalation pathways Track global patient registries metrics provide dashboards collaboratio ...

+ Lead planning and management of complex patient registries across multiple regions · + Develop project plans and risk management strategies to ensure registry deliverables are achieved · + Oversee site feasibility selection initiation monitoring and close-out activities in coll ...

+Job summary · Revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs. · +ResponsibilitiesProvide leadership, direction, and oversight for complex global patient registries. · ...

The Senior Clinical Study Manager will provide leadership and direction for a complex global patient registries within the MedAlliance LLC / Cordis SelutionSLR portfolio. · Lead the planning and initiation of assigned global patient registries duties across multiple regions. · De ...

Selution partners Cordis in developing advanced drug device combination products. The Senior Clinical Study Manager will lead complex patient registries. · ...

The Los Angeles Sales Manager is responsible for driving the overall growth of the company's U.S. study abroad business. This includes business planning market promotion channel development team management and full-cycle client service oversight. · Develop strategic plans for U.S ...

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 Clinical Research Associate (CRA) is responsible for the successful execution of clinical trials. This role will proactively resolve study site issues and participate in process improvement initiatives as applicable. · ...

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. · ...

Kelly Science and Clinical FSP is currently seeking a Clinical Study Assistant for a long-term engagement in Irvine, CA with one of our Global Medical Device clients. · ...

The company is seeking a Clinical Study Assistant for a long-term engagement in Irvine, CA. The role will provide administrative and organizational support for assigned clinical trials. · ...

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 ...

The role involves the successful execution of clinical trials and proactive resolution of study site issues. The CRA engages with investigators and stakeholders as a member of the Clinical Trial Development and Operations team. · ...

This role will proactively resolve study site issues and participate in process improvement initiatives as applicable. The CRA engages with study investigators, vendors, and internal/external stakeholders as a member of the Clinical Trial Development and Operations team. · ...

The Clinical Research Specialist (CRS) is responsible for supporting and/or conducting clinical study activities and basic data collection at clinical sites. · Plan, implement and conclude clinical studies in support of project timelines/market release goals. · ...

The Clinical Research Specialist (CRS) is responsible for supporting and/or conducting clinical study activities, · Plan, implement and conclude clinical studies in support of project timelines/market release goals. · Prepare and document study plans, contracts, budgets... · ...

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