Our early stage start-up client is adding a Senior Clinical Research Associate to the team. The Sr. CRA assists with the planning and development of high-quality clinical activities to support projects. The Sr. CRA has strong clinical research experience, and a strong understanding of research methodology, regulations, and guidelines. The Sr. CRA has experience assisting with the development of clinical strategies and/or plans, protocol development and execution, monitoring, and ensuring data quality and management of clinical studies. The Sr. CRA is recognized as a subject matter expert with CROs and other vendors in the execution of clinical trials and interacts with study investigators and other study staff members. The Sr. CRA will monitor clinical research sites in accordance with FDA Regulations, other global regulatory bodies, GCP and ISO compliance, and company SOPs.
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