Position: Associate Analyst, Clinical Operations Req#: 9697-1
Location: Irvine, CA (100% onsite only)
Duration: 12+ Months Contract (Part-Time job, 20 hours per week)
Part-time work schedule: PT work schedule to 4 days on-site/week (8 AM-12 PM) with the flexibility to WFH on Fridays OR candidates can choose to work 2.5 full days each week (e.g. Mon, Weds + Thurs only) instead of splitting the 20 hours across 5 days if that is their preference.
More on this position:
What does your group do? The group will be supporting advanced patient monitoring rather than Critical Care
Does your team use any specific technology/software you want us to look out for? JDE, SharePoint, MS Office Suite, EDC, TMF, CTMS
What will a typical workday look like? Clinical study device management activities such as ordering devices, coordinating international and domestic shipments, facilitating the return of study devices and equipment, managing clinical study and research laboratory device inventory, completes associated clinical study documentation as needed. This is a collaborative role, which requires solid communication skills and very good attention to detail.
Will there be any travel involved? Yes,
We need someone with a vehicle as they may need to travel between the two campuses.
Travel frequency: Could be once a month, could be twice a week (per business need)
Will you consider remote work? If yes, will they need to be in a specific time zone? No remote work
What are your top 3 required technical skills? Must haves? Preferred technical skills : Clinical research coordination, clinical study management, study document (e.g. ICF) and CRF (case report form) review
What are nice to have skills ? EDC, CTMS, Veeva (TMF), GCP training, experience with medical device studies
Is there anything that would automatically disqualify a candidate? No prior clinical research experience
Job Description:
Education and Experience:
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