Our Clinical Research Associates (CRA) are home-based. Worldwide offers a wide range of industry-best benefits that include unlimited PTO, 10 paid holidays and matching 401(k).
To be considered for the CRA role, candidates will ideally have 5 years of experience in field monitoring for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). Our CRAs are responsible for the quality of data submitted from study sites. In addition, CRAs must assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
Experience in Oncology is required.
Requirements:
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