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Job description
Parexel FSP is seeking a Site Activation Partner I to lead or support operational activities from start up to close out for assigned studies across sites. You will ensure regulatory compliance, manage IIP and regulatory submissions, and collaborate with cross-functional teams to meet study timelines.
The role requires at least 2 years of startup experience and familiarity with US/Canada regulatory processes, with a potential transition to a full-time role after the 7-month temporary assignment.
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Worksite address
california, MO, 65018, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.