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Advanced Clinical

Global Project Manager

Advanced Clinical, Oro Valley, Arizona, United States

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Overview

We are currently searching for a skilled professional to join a well-known client’s team as a Global Project Manager in Tucson, Arizona. The Global Project Manager role will be responsible for driving the delivery of innovative Companion Diagnostics projects and ensuring optimized product development across our portfolio. Acting as a trusted advisor, you will manage projects from concept through commercialization, enabling teams to work efficiently while responding quickly to evolving business needs. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. Responsibilities

Lead and manage complex projects, ensuring on-time, on-budget, and high-quality delivery. Develop and maintain integrated project plans, including timelines, resources, budgets, and dependencies. Drive effective communication and alignment with internal stakeholders and external pharma partners. Implement robust project management practices, including risk management, scenario planning, and critical path analysis. Lead milestone and capacity reviews (e.g., cQCR, SCR, fQCR) and support decision-making at the portfolio level. Apply hybrid project methodologies, balancing Agile and traditional practices as appropriate. Foster cross-functional collaboration, lead team meetings, and drive knowledge sharing. Define and monitor KPIs, OKRs, and metrics to ensure continuous improvement in project quality and efficiency. Act as the single point of contact for project/program data, enabling clear reporting and decision-making. Experience

4+ years of project management experience in diagnostics, medical devices, health sciences, biotech, or pharmaceuticals (experience in other regulated industries considered). 1+ year of experience in clinical biomarker or IVD/Companion Diagnostic development, validations, regulatory submissions, or instrument development. Education

Minimum of Bachelor’s Degree in science, engineering, or business-related field required, Master’s degree or PMP certification preferred To Be a Best-fit Your Strengths Must Include

Strong knowledge of healthcare quality, risk, and regulatory compliance (e.g., FDA 21 CFR Part 820, ISO 13485, ISO 9001). Demonstrated ability to lead complex projects from concept to commercialization. Skilled in project management tools (Planisware, MS Office, G-Suite, Trello, Jira, Smartsheet, Azure DevOps, etc.). Strong analytical, problem-solving, and critical thinking abilities. Excellent communication and interpersonal skills; proven ability to influence and drive decisions across stakeholders. Familiarity with Design Control and Phased Development processes. Experience applying Agile methods in a hybrid environment. About Advanced Clinical

Advanced Clinical is an award-winning clinical development organization that provides global services including CRO, Functional Support, Quality & Validation, Patient Recruitment and Retention, and Strategic Talent Acquisition solutions for pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations. Our mission is to deliver a truly better clinical experience for our clients and candidates. To learn more about Advanced Clinical which has been named to Chicago Tribune’s Top Workplaces, Chicago’s Best and Brightest Companies, and Best of Staffing Talent & Client, visit http://www.advancedclinical.com. Regarding your application

Please know that every completed application is carefully reviewed by the Advanced Clinical recruitment team. We understand the time commitment that is needed to prepare an application, so we respect your effort by thoughtfully reviewing and responding to each application. In return, we ask for your patience as careful review takes time, and we may not be able to respond to every application immediately. Seniority level

Mid-Senior level Employment type

Full-time Job function

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