Responsibilities: for the Oncology Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote and on-site monitoring and study activation Participate in the development of study tools, protocols, and clinical trial documentation Some travel required once travel bands are lifted Qualifications: for the Oncology Clinical Research Associate: 3+ years of Oncology on-site Monitoring and hands on experience with EDC Systems Experience with Phase 1 Oncology is non-negotiable Organization to perform monitoring duties across multiple sites is a must
| Location | Boston, MA |
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