Clinical Research Associate - Ohio Region

Role: Clinical Research Associate (CRA) supporting site-level oversight in clinical trials across all phases. Objectives: ensure trial quality, compliance, data integrity, and patient safety at clinical sites. Responsibilities: conduct site qualification, initiation, monitoring, and close-out visits; verify data accuracy; ensure adherence to ICH GCP, SOPs, and regulations; foster relationships with sites and internal teams; support investigator assessment and site selection; assist in audit readiness and regulatory compliance; and manage study drug/IMP oversight. Qualifications: Bachelor’s degree in life sciences or related, with 2-3 years of clinical research experience; proficiency in clinical systems (e.g., CTMS, eTMF, RBQM tools); strong understanding of GCP, regulations, and data analysis; excellent communication and organizational skills; ability to work independently and manage multiple protocols. Preferred: experience with remote/risk-based monitoring, AI tools, and working across multiple therapeutic areas. High-value: role involves up to 70% travel, supports diverse clinical trial activities, and emphasizes data integrity and compliance within biopharma settings. Work setup: based in Ohio with extensive travel.