• Lead and coordinate central laboratory activities across clinical trial programs • Monitor and manage all aspects of designated clinical trial protocols in Global Central Labs • Provide oversight and coordination of study initiation • Review, interpret, translate and program study protocols into a complete and accurate database • Communicate with internal departments and external vendors to ensure project requirements are understood • Facilitate the flow of technical and clinical laboratory information to all stakeholders • Assure compliance with FDA and Good Clinical Practice guidelines

• Work as part of a global healthcare intelligence and clinical research organization • Help deliver new medicines and treatments to patients faster • Collaborate with team members across different countries

• Manage clinical trial biospecimen projects • Collaborate with cross-functional teams • Ensure compliance with regulatory standards • Oversee timelines, budgets, and project objectives

• Manage day-to-day project and programme management activities, supporting your team to deliver quality outcomes • Developing and executing project plans, focusing on achieving project goals and objectives • Leading cross-functional teams to ensure the successful implementation of project activities • Collaborating with stakeholders to identify project requirements and define project scope • Mentoring and guiding team members, fostering a culture of excellence and continuous improvement • Driving the development of project documentation and reports to present findings to stakeholders in a clear and actionable manner • Staying abreast of industry trends and emerging technologies to integrate best practices into project management strategies • Contributing to organizational growth through effective project leadership and strategic planning