Beacon Hill Staffing Group drives clinical operations for leading biopharma clients across the US. This Clinical Trial Associate supports execution of multi-site trials in oncology therapeutics. Coordinate site start-up activities, including contract negotiations and IRB submissions. Track patient enrollment metrics and resolve data discrepancies from EDC systems daily. Assist in preparation of study progress reports for sponsors. Candidates hold a Bachelor's in life sciences or nursing. Require 1-2 years in clinical research coordination. Proficiency in Medidata Rave and Veeva Vault essential. Familiarity with FDA regulations a plus. Excel in detail-oriented tasks. Demonstrate strong organizational skills. Dynamic, collaborative environment. Competitive compensation package.