• Gather and analyze data to estimate the costs associated with projects, including labor, materials, and overhead expenses • Analyze blueprints and other documentation to prepare detailed time and cost estimates • Occasionally meet with clients to discuss project details and requirements, ensuring a clear understanding of expectations • Work closely with all departments, engineers, architects, contractors, and other stakeholders to formulate accurate estimates and resolve any issues • Prepare and present detailed cost reports and proposals to clients, outlining the breakdown of costs • Stay updated on industry trends, pricing, and market conditions to ensure competitive and accurate estimates • Use specialized software for data analysis, cost estimation, and project management • Other duties as assigned

This role involves transforming educational organizations through innovative strategies and solutions, making significant impacts on student outcomes and institutional effectiveness. Lead complex, multidisciplinary clinical research consulting engagements from scoping through delivery and measurable impact. Set strategic direction across client engagements and portfolios by prioritizing initiatives, aligning work to institutional goals, and guiding enterprise-scale transformation within academic medical centers and research enterprises. Serve as a trusted advisor to university and hospital leadership on research strategy, governance, and regulatory compliance. Build and manage a portfolio of client relationships to drive repeat work, expansion opportunities, and sustained client advocacy. Develop, mentor, and retain high-performing teams by defining roles, providing coaching and feedback, and fostering a strong culture of collaboration. Contribute to firm-wide initiatives by shaping offerings, sharing expertise, and advancing strategic priorities.

In this exciting role as a Clinical Research Specialist, you will have primary focus responsibility in preparing sites for data collection, relationship building with research coordinators, regulatory report writing, and data cleaning. The CRS works under the direction of a Clinical Study Manager and assists with numerous tasks associated with the execution of a clinical trial. The Study & Scientific Solutions (S&SS) is a function within Medtronic Core Clinical Solutions (MC2). S&SS is an internal service provider to all of Medtronic and assigns resources to assist Business Units execute on clinical trials and scientific projects when they have an increase in workload. This position is remote to enhance our competitive edge and expand our cross-functional collaboration efforts. This role will require 10% of travel to enhance collaboration and ensure successful completion of projects. Oversees, designs, plans and develops clinical evaluation research studies. Prepares and authors protocols and patient record forms. Conducts registered and non-registered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential. Oversees and interprets results of clinical investigations in preparation for new drug device or consumer application. Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations, and may prepare clinical trial budgets. May be responsible for clinical supply operations, site and vendor selection. Represents Medtronic from a clinical research perspective within the country/region and collects feedback from local customers and authorities. Builds and maintains optimal relationships and effective collaborations with various internal and external parties. Drives local evidence dissemination & awareness.

• Join our Clinical Research team as a Principal Scientist in Biostatistics • Contribute to advancing life-changing therapies through statistical excellence • Work closely with clients while utilizing the benefits and resources of Thermo Fisher Scientific • Responsible for implementing diverse statistical tasks throughout the full clinical trial process, from study design and protocol writing to final analysis and reporting • Opportunity to impact health outcomes while working with advanced clinical development programs