Associate II, Field Clinical Monitoring - Aliso Viejo, CA

+Responsible for driving study execution and operational excellence in accordance with ICH Good Clinical Practices, FDA regulations, guidance documents, and company SOPs. · ...

Responsible for driving study execution and operational excellence in accordance with ICH Good Clinical Practices, FDA regulations, guidance documents, and company SOPs. · ...

+ Associate II Field Clinical Monitoring · Responsible for driving study execution and operational excellence in accordance with ICH Good Clinical Practices FDA regulations guidance documents and company SOPs. · + Provide oversight of site compliance with study protocols informed ...

The Sr Associate Field Clinical Monitoring will be responsible for driving study execution and operational excellence in accordance with ICH Good Clinical Practices FDA regulations guidance documents and company SOPs. · Identify develop and maintain investigators and sites capabl ...

Responsible for driving study execution and operational excellence in accordance with ICH Good Clinical Practices, FDA regulations, guidance documents, and company SOPs. Provide oversight of site compliance with study protocols, informed consent procedures, and data integrity req ...

Responsible for driving study execution and operational excellence in accordance with ICH Good Clinical Practices, FDA regulations, guidance documents, and company SOPs. · ...

The Front Office Assistant performs clerical duties and front office operations in support of patient care activities. · ...

UCI Health is the clinical enterprise of University of California · Irvine-based healthcare system providing tertiary care services. · Clinical nurse will collaborate with interdisciplinary teams. · ...

The clinical nurse will collaborate with interdisciplinary teams to develop and implement a plan of care for a specific group of assigned patients. · Performs professional nursing duties that incorporate the psychomotor and age appropriate cognitive skills of the patient/family/s ...

The clinical nurse will collaborate with interdisciplinary teams to develop and implement a plan of care for a specific group of assigned patients. · To learn more about UCI Health visit Responsibilities: · ,Qualifications: · ,Licenses and Certifications: · ,Total Rewards: · ...

The Front Office Assistant performs a variety of clerical duties and front office operations in support of the patient care activities ensuring even patient flow and continuous communication within the department · Greets visitors and answers telephones. · Collections Copays, clo ...

The Clinical Research Associate (CRA) will join our Clinical Operations team in a hands-on role supporting the planning, execution, and monitoring of clinical trials. · ...

The Clinical Research Associate will join our Clinical Operations team in a hands-on role supporting the planning, execution, · and monitoring of clinical trials.Conduct site monitoring visits (initiation, · routine, and close-out) to ensure compliance with the clinical protocol, ...

The Clinical Research Director will lead cutting-edge clinical studies that push the boundaries of ophthalmic innovation. They will shape the future of eye care from product development through clinical trials. · ...

The Sr. Scientist II reports to the Sr. Director of Toxicology and Biocompatibility and is responsible for providing subject matter expertise and leadership in toxicology and nonclinical development at the team level. · ...

The Clinical Trials Associate II is responsible for the coordination of clinical research studies in compliance with U.S. and international regulations under the guidance of a Clinical Manager or Clinical Director. · ...

The Clinical Trials Associate II is responsible for coordinating clinical research studies in compliance with U.S. and international regulations under the guidance of a Clinical Manager or Clinical Director. · Key responsibilities include: · Clinical Study Preparation and Mainten ...

+Lead the strategic planning and operational execution of clinical trials within the neurovascular therapeutic area. · +Lead Clinical Operations teams for effective study execution. · ...

The Sr. Clinical Supply Manager has responsibility for assuring investigational product for any given clinical study is available at the clinical investigative site at the time needed for study use in study subjects, and in the condition required for human use, in an efficient an ...

The Clinical Supply Director is responsible for providing strategic and operational leadership to ensure investigational product availability for all Glaukos clinical studies. · ...