Global Project Manager - Companion Diagnostics / Personalized Hea...
MedStar Health - Tucson, Arizona, United States, 85718
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Overview
Global Project Manager - Companion Diagnostics / Personalized Health Care Join Roche, where we value personal expression, open dialogue, and genuine connections. Our mission is to prevent, stop, and cure diseases, ensuring access to healthcare for all now and in the future. The Role: The Global Project Manager (GPM) plays a key role in product delivery within the Project Management Chapter. Responsible for managing projects from concept to completion, developing detailed work plans, schedules, and resource allocations. Acts as a trusted advisor, translating projects into products and enabling effective use of organizational resources. Key Responsibilities: Manage project structures for Companion Diagnostics product development and care, including communication, timelines, resources, budgets, and risk management. Create and maintain integrated project plans, ensuring quality in risk management, critical path analysis, and planning. Drive project execution, manage milestone preparations, and lead continuous improvement initiatives. Apply appropriate project methodologies, including agile practices, and coach teams accordingly. Establish and report on KPIs, OKRs, and other metrics to measure project performance and quality. Act as a trusted advisor on project planning, risk management, and portfolio optimization. Lead project team meetings, facilitate knowledge sharing, and identify areas for process improvement. Manage project data and support decision-making at various organizational levels. Collaborate with cross-functional teams and leadership to ensure project success. Other duties as assigned. Qualifications: Bachelor's degree in Life Sciences or related field. Minimum 4 years of project management experience in the diagnostic, medical device, pharmaceutical, or biotech industry. At least 1 year of experience in clinical biomarker, In Vitro Diagnostic development, or related areas. Experience in regulated industries such as FDA or ISO standards. Preferred: Master's degree or Ph.D. with additional relevant experience. Experience in clinical biomarker or diagnostic development, regulatory submissions, or program management. This is a hybrid role based in Oro Valley, AZ, with an expected on-site presence of approximately 2 days per week. Compensation ranges from $100,000 to $186,000, with potential bonuses and benefits. Roche is an equal opportunity employer and committed to diversity and inclusion. For accommodations during the application process, please contact us accordingly.
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