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The Bioanalytical Scientist at Precision for Medicine is responsible for designing and performing experiments, analyzing data, managing staff, and improving assay procedures. The role involves troubleshooting scientific issues, collaborating with technical teams, and supporting project report writing and publications.

The Principal Scientist will supervise laboratory staff in bioanalytical activities. Responsibilities include leading bioanalysis and biomarker projects, designing experiments, maintaining lab safety practices, and collaborating with technical teams. The role requires troubleshooting assays and developing SOP documentation, as well as providing technical expertise to clients.

The Resource Manager oversees and optimizes resource allocation for projects, manages staffing processes, and develops resourcing strategies to meet organizational needs. The role includes advising on resource management, coordinating with HR and Finance on hiring plans, and contributing to budgeting and forecasting.

The Customer Success Manager at QuartzBio will drive customer retention and growth by leading onboarding, managing relationships, resolving issues, and monitoring customer engagement metrics while facilitating user adoption and advocating for customer needs.

The Principal Quality Assurance Auditor oversees quality and compliance activities during clinical studies, serving as a subject matter expert. Responsibilities include supporting the Q&C team, conducting audits, coordinating vendor assessments, and providing training and guidance on quality systems while ensuring adherence to regulations.

The Commercial Strategy & Optimization Lead provides strategic guidance to enhance the effectiveness of the Commercial organization, collaborates with leaders across functions, and drives projects to improve commercial impact. Responsibilities include developing commercial strategy, improving sales opportunities, and managing multiple projects effectively.

The Safety Specialist II is responsible for processing and evaluating Serious Adverse Event reports, providing safety expertise, mentoring new staff, and interfacing with sponsors and vendors. The role supports the design and implementation of safety collection tools and reporting systems, with a strong focus on regulatory compliance and project-specific guidelines.