Quality Control Associate

How You’ll Spend Your Day Perform all activities/procedures in strict compliance with the study protocol, GCP, GDP, SOPs, QA/QC procedures, OSHA guidelines, and other applicable state/local regulations. Support the clinical operations team in reviewing essential clinical documents for accuracy. Assist in the development and implementation of quality control procedures and processes. Collaborate with study teams to identify and resolve quality issues. Record, track, and ensure resolution of data queries. Understand protocol-driven timed study events and acceptable collection windows. Proactively communicate issues and/or problem resolutions to supervisors and managers. Perform general administrative tasks when required. Other tasks as assigned by management. Education High school diploma or equivalent required. Knowledge, Skills, and Abilities Exceptional customer service and professionalism. Effective communication (oral, written, interpersonal) with internal/external parties. Ability to work independently and in a team environment. Professional sensitivity to confidential material/information. Ability to prioritize and manage workloads under tight deadlines. Strong organizational/time-management skills and attention to detail. Proficient in MS Office Suite (Word, Excel, Outlook, PowerPoint). Physical Demands Extended periods of sitting/standing/walking/stooping/bending. Lift materials and supplies up to 50 pounds. Routine keyboarding. Also Good to Have 1–3 years of experience in a clinical research/clinical/medical environment. Knowledge of quality control procedures. CCRC preferred. Benefits Comprehensive Health Insurance (medical/dental/vision/prescription) starting first day if enrolled. Retirement Savings (401(k) with employer match and defined contribution). Paid Time Off. Company-paid Life and Disability insurance. Additional listed benefits. #J-18808-Ljbffr Scorpion Therapeutics