Associate Director, Clinical Operations Program Lead

Role: Associate Director, Clinical Operations Program Lead in Oncology, responsible for developing and executing operational strategies for clinical programs. Objectives include ensuring timely, high-quality trial execution within budget, and representing Clinical Operations at the program level. Responsibilities encompass collaborating with cross-functional teams, overseeing CROs and vendors, budget management, risk assessment, and contributing to regulatory readiness and inspection activities. Qualifications: Bachelor's degree in Life Sciences or related field; 10+ years in pharma/clinical research, including 7+ years managing Phase 2 or later clinical studies; experience in multiple therapeutic areas preferred. Skills include program management, global regulatory knowledge (US CFR, EU CTD, ICH GCP), leadership, influence without authority, and excellent communication. High-value biopharma specifics: oncology focus, global Phase 2+ programs, cross-functional strategic initiatives, and vendor oversight. Work setup is remote with Massachusetts location reference; travel is not specified.