CRA II, Onc/Neuro/Rare/Derm (West Coast, Midwest, Northeast)

Role: CRA II specializing in Oncology, Neurology, Rare Diseases, or Dermatology, supporting clinical trial monitoring across West Coast, Midwest, and Northeast regions. Responsibilities: conduct all monitoring visits (qualification, initiation, interim, close-out) both remotely and onsite, ensure data quality and patient safety per ICH GCP/ISO14155, manage queries, maintain TMF/eTMF, and oversee site documentation and IP accountability. Support project teams through communication, training, and administrative tasks; may serve as SME and support feasibility assessments. Requirements: undergraduate degree or health-related license; 2+ years of clinical trial experience with proven CRA success; strong knowledge of ICH GCP, FDA/EU regulations, ISO14155; ability to manage multiple priorities in a fast-paced environment; willingness to travel 70-85%, valid driver’s license, passport. Preferred: experience in Oncology, Rare Disease, Neurology, or Dermatology; team leadership skills; regional and cultural knowledge. HighValue: Oncology, Rare Disease, Neurology, Dermatology; clinical monitoring; GCP/ISO14155 compliance; remote and onsite visits; high travel (70-85%). WorkSetup: primarily field-based in specified U.S. regions.