Job Details

<Key Responsibilities>

・Contributes to protocol, ICF, IB and Reg submission creation

・Executes CDAs and supports creation of CSAs and site budgets

・Attends Clinical Project Meetings and manages Meeting Minutes

・Executes study payments, manages device tracking/accountability and responsible for site management activities

・Uses internal systems to update project milestones and study timelines

・Manages Master study file

・Creates site Regulatory binders and other site materials

・Manages and controls CROs for site management including monitoring

・Manages 3,4 people





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