Clinical Research Associate - Ohio Region

Role: Clinical Research Associate (CRA) responsible for site monitoring and ensuring compliance with GCP, SOPs, and regulations across all trial phases. Responsibilities include conducting site qualification, initiation, routine visits, and close-out; verifying data integrity; maintaining site adherence to regulatory standards; fostering relationships with internal teams and external sites; supporting site selection and performance management; and participating in audits and regulatory inspections. Qualifications: Bachelor's degree in life sciences or related field; 2-3 years of clinical research experience, preferably within pharma/biotech, with understanding of clinical processes and regulations; proficiency in clinical systems (CTMS, eTMF, eDC, RBQM); strong communication, organizational, and analytical skills; ability to work independently and manage multiple protocols across therapeutic areas. High-Value: Up to 70% travel; experience supporting diverse trial phases; knowledge of electronic systems; ability to manage documentation and site performance metrics; familiarity with risk-based monitoring approaches. Work Setup: Travel-intensive role primarily in Ohio, with a focus on site monitoring in clinical trials.