Senior Clinical Trial Management Associate

A Sr. Clinical Trial Management Associate job in Irvine, CA is available through Adecco Medical and Science. You must possess your bachelor’s degree in a science or health related field and have prior experience working on a clinical study. You will be responsible for assisting the Clinical Trial Manager in the operational execution of clinical studies.

Sr. Clinical Trial Management Associate) job responsibilities include:

• Assist with regional study feasibility, the initial assessment of
vendors, supplies planning
• Assist with the development of study specific documents such as
informed consent
• Assist with regional investigator meetings, developing enrollment
initiatives and planning clinical study supplies
• Assist with regional financial management, database lock activities,
study drug management, trial master file management, study
enrollment management
• Assis with ongoing review of protocol deviations, regional vendor
management and ensure adverse event reporting
• Ensure all documents are filled in the TMF appropriately, ensure all
close out activities are complete, ensure proper documentation
• Report any potential GCP violations


• Bachelor’s degree in a science or health related field
• Previous experience working on a clinical study
• Oversight or mentoring of more junior study monitors preferred
• Prior experience in device clinical research, ophthalmology and/or
medical aesthetics is a plus
• Understanding of Good Clinical Practices, ICH guidelines, PhRMA
code, CFR Guidelines, HIPAA

If you are interested in this Sr. Clinical Trial Management Associate job in Irvine, CA then please click APPLY NOW. For other opportunities available at Adecco Medical and Science go to If you have questions about the position or would like more information, please contact Kayla Hanscom at (858) 812-2600 or by email at
Equal Opportunity Employer Minorities/Women/Veterans/Disabled

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Reference number US_EN_2_108175_331141