Sr. Clinical Research Associate - Oncology (East Coast)

Responsibilities: of the Senior Clinical Research Associate: • Independently manage investigative sites from initiation through closeout. • Conduct onsite and remote monitoring visits, including SIVs, IMVs, and COVs. • Perform source data review/verification and ensure data quality and protocol compliance. • Monitor site performance, enrollment, deviations, queries, and AE/SAE documentation. • Maintain accurate study documentation within CTMS, EDC, eTMF, and site files. • Build strong relationships with investigators and site staff while identifying and escalating study risks. Qualifications: of the Senior Clinical Research Associate: 3+ years of independent clinical monitoring experience. Oncology clinical trial monitoring experience required. Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes. Experience independently managing multiple investigative sites. Strong communication, organization, and site management skills. East Coast based with ability to travel to investigative sites as required. Compensation: of the Senior Clinical Research Associate: Salary: $140,000-$150,000 annually Reginal Travel Required Comprehensive Benefits: Medical, Dental, Vision, 401(k), Sick Leave (as required by law), and Paid Holidays Application Period: This position opens for applications on 9/30/2026 and will remain open for a minimum of 30 days from the posting date.