Oncology Trials Pre-Screening Data Specialist

A health technology startup in California seeks a Pre-Screening Clinical Data Coordinator to enhance access to cancer trials. The ideal candidate will translate clinical trial protocols into structured data and collaborate with clinical teams. Responsibilities include data abstraction, quality control, and report preparation. Candidates must have at least 2 years of clinical research experience, strong detail orientation, and familiarity with medical terminology. A Bachelor's degree is required. The role supports a mission of equity in cancer care. #J-18808-Ljbffr