Sr. Clinical Trial Associate

Role: Senior Clinical Trial Associate supporting clinical operations for Summit’s oncology Phase 3 studies in NSCLC and colorectal cancer, focusing on study documentation, vendor oversight, and cross-functional coordination. Responsibilities: manage study trackers, oversee eTMF, support site start-up and monitoring activities, coordinate with CROs, and contribute to process improvements. Requirements: Bachelor's degree in life sciences or related field; 4+ years of clinical study experience within CRO or pharma; proficiency with CTMS and eTMF systems; strong knowledge of GCP, FDA regulations, and clinical development processes. HighValue: oncology (NSCLC, CRC), Phase 3 trials, regulatory compliance, vendor coordination, cross-functional teamwork. WorkSetup: onsite in Princeton, NJ or Miami, FL.