Director, Medical Evidence Generation Operations Lead (Multiple Openings)

Role: The Director MEG Operations Lead provides strategic and operational leadership for the Medical Evidence Generation (MEG) trial portfolio within a therapeutic area, ensuring studies are executed efficiently, on time, within budget, and compliant with regulatory standards. Responsibilities include managing and developing a team of Global Trial Leads, overseeing all studies in the portfolio, ensuring quality and regulatory adherence, and driving operational excellence and standardization. The role involves strategic planning, resource management, risk mitigation, and stakeholder engagement across internal teams and external vendors, including CROs. It also entails budget oversight, lifecycle management of studies, and representing MEG Operations in governance forums. Requirements: BA/BS in relevant field, with a minimum of 9 years in clinical/medical operations and project management in the biopharma industry, including experience managing global trials and leading teams. Experience with CRO/vendor management is preferred. The role demands strong leadership, project management, risk management, and cross-functional collaboration skills. High-Value: Focus on medical evidence generation within a pharmaceutical context, leading global studies, with an emphasis on operational excellence, compliance, and strategic oversight in a complex matrix environment. Work setup: Not specified; travel up to 25% may be required.