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

Role: Senior Clinical Research Associate (CRA) supporting monitoring activities across Phase I-IV clinical trials, including device trials, in oncology, neurology, rare diseases, and dermatology. Responsibilities: perform on-site and remote site monitoring visits (qualification, initiation, interim, close-out), ensure data integrity and patient safety per ICH-GCP/ISO standards, serve as primary site contact, manage queries, support Trial Master File activities, and identify risk or training needs. Requirements: undergraduate degree or equivalent, 4+ years of on-site clinical research monitoring experience, strong customer-focused communication skills, and experience in oncology, neurology, rare disease, or dermatology studies. Preferred: ability to meet 8-10 monitoring visits/month, 70-85% travel, residence on West Coast, Midwest, or Northeast, and valid driver’s license/passport. HighValue: oncology, neurology, rare disease, dermatology, Phase I-IV, remote and on-site monitoring, multi-region locations, 8+ years of clinical monitoring experience, and strong site management skills. WorkSetup: remote and on-site with travel.