Provides overall support to study sites and clinical project teams engaged in clinical research studies, adhering to applicable protocols, SOPs, and regulatory requirements. Acts as point of contact for study sites and expected to work independently in providing support to CRA and sites. Can have increased focus on training and development of junior staff members and can act as Lead In-house CRA.
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You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas and assist other CRAs with co-monitoring activities both remote and on-site. As the CRA you are the main sponsor representative, providing key project updates. You will collaborate with the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely.