The Principal Trial Manager is responsible for leading projects and initiatives to improve the quality and compliance of the data management functional areas in addition to the regular responsibilities as an individual Trial Manager. The Principal Trial
COA Sr. Specialist is responsible for providing end-to-end COA systems project management support including, but not limited to, gathering study-specific user requirements, executing UAT tasks, managing project timelines, managing and enforcing COA systems Standards. COA Sr.
The Sr Specialist within Operational Enablement & Effectiveness (OEE) / MAP has experience in clinical operations and is responsible for the development of data analysis and visualizations in support of user needs across Global Clinical Trial
The Director, Portfolio & Resource Operations, Global Data Management and Standards (GDMS) Clinical Data Management (CDM) provides leadership and governance for capacity planning, resource forecasting, and portfolio performance management across CDM. This role drives standardization of
The Specialist within Operational Enablement & Effectiveness (OEE) / MAP has experience in clinical operations and is responsible for the development of data analysis and visualizations in support of user needs across Global Clinical Trial Operations
Under the direction of Clinical Data Management and GDMS leadership, the Director, Clinical Data Management Indication Lead, Late Oncology provides operational leadership for data management delivery within an assigned indication(s) for a therapeutic area. The role
We are seeking a professional to act as a Procurement Fleet Specialist in Latin America, leading initiatives, projects, and vendors related to fleet management and corporate services. This position requires strong relationship-building skills, stakeholder management, problem-solving,