Sr. Clinical Research Associate
ICON · CA +3 more
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Role summary
This position involves serving as the primary liaison between investigational sites and sponsors for an oncology trial, conducting site visits and ensuring regulatory compliance. The role requires monitoring patient safety, managing drug accountability, resolving data queries, and supporting recruitment efforts across the West region. Candidates need 3+ years of on-site monitoring experience in myelofibrosis trials, proficiency with ICH-GCP standards, and willingness to travel up to 50%.
Privacy & handoff
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