Associate Clinical Trials Director

Role: Associate Director of Clinical Operations responsible for managing and executing all phases of clinical studies for neurobiological and psychiatric therapeutic areas, with a focus on ensuring compliance with regulatory standards (FDA, EU, GCP). Responsibilities: lead clinical trial management, oversee CRO/vendor relationships, develop strategic plans, and support career development of clinical staff; ensure trials adhere to timelines, budgets, and quality standards; facilitate cross-departmental collaboration (Regulatory, QA, Data, Stats); implement process improvements and establish performance metrics. Requirements: BS/BA with 12+ years (or Master’s with 10+ years) experience in clinical trial management, including CRO/vendor oversight, monitoring budgets, and site management; extensive knowledge of ICH, GCP, FDA regulations, and EU directives; expertise in global studies, particularly in endocrine or rare disease indications; strong leadership, project management, and communication skills; proficient in data analysis and process optimization. HighValue: experience in endocrine-related or rare disease clinical trials, global study oversight, vendor management, and regulatory compliance. WorkSetup: not specified, but implies leadership in a multi-disciplinary, possibly hybrid environment.