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As a Clinical Research Associate I, you will communicate with project stakeholders and help ensure timelines, targets, and standards are met across clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators, with a focus on subjects’ rights, safety, and well-being, as well as data quality and compliance. The role includes onsite monitoring, study startup activities where applicable, site management, and collaboration with internal teams and support services. You will receive support from a knowledgeable and professional team and develop a variety of skills while progressing with the company and contributing to challenging, full-scale projects.
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Job Type
Full-time
Career Level
Entry Level

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