Clinical Trial Associate or Senior Clinical Trial Associate

Role: Clinical Trial Manager supporting global Phase 2 clinical trials for a biopharma focused on targeted protein degradation (TPD), primarily small molecule degraders. Responsibilities: oversee trial planning, vendor management, study-specific meetings, protocol and CRF design input, training, site selection, monitoring, data quality, and safety review; collaborate with data management, translational medicine, and CRO teams. Qualifications: Bachelor’s in Life Sciences; 3+ years (CTM) or 5+ years (Sr. CTM) experience managing large, complex Phase 2 trials; strong knowledge of GCP, regulatory guidelines, and clinical operations; excellent leadership and communication skills. HighValue: global Phase 2 small molecule degrader trials, complex trial management, cross-functional collaboration, vendor oversight, bioanalytical sampling integration. WorkSetup: not specified, but implied to be a fast-paced environment with cross-functional teams.