Clinical Trial Associate or Senior Clinical Trial Associate

Role: Clinical Trial Manager supporting global Phase 2 clinical trials for a biopharma focusing on targeted protein degradation therapies. Responsibilities include trial planning, vendor management, study execution, site qualification, monitoring, data review, and ensuring compliance with regulatory standards like ICH GCP and HIPAA. The role involves collaboration with CROs, data management, translational medicine, and medical monitoring teams to ensure trial integrity, safety, and timely delivery. Qualifications: Bachelor's in Life Sciences; 3+ years (CTM) or 5+ years (Sr. CTM) experience managing complex, large-scale Phase 2 trials in biotech/pharma. Skills in project management, regulatory compliance, data review, and cross-functional team leadership are essential. Preferred: experience in early- to mid-phase clinical development, strong problem-solving, and communication skills. HighValue: global Phase 2, biologics or small molecule therapies, regulatory compliance, cross-functional collaboration, vendor management, experience with bioanalytical sampling plans. WorkSetup: not specified, but implies a fast-paced clinical environment with multi-team interactions.