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Worldwide Clinical Trials is hiring a Senior Clinical Research Associate (CRA) to manage research activities at sites participating in its clinical research projects, with required experience in CNS. The CRA typically contributes throughout the clinical study lifecycle, from identifying potential sites and supporting study start-up through site maintenance and closeout. The role includes conducting study initiation visits and ensuring sites follow requirements for informed consent, safety-event reporting, and applicable regulations. Most site management is performed remotely, with regional travel required. The position is part of Clinical Operations at a global CRO with more than 4,000 professionals. CRAs work with colleagues across therapeutic areas and receive support in regulatory submissions, Trial Master File (TMF) management, and in-house CRA support for projects with significant site-management needs. Regular coaching and touchpoints with a Line Manager support professional development, with a career path that can lead to Clinical Trial Manager roles.
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Job Type
Full-time
Career Level
Senior

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