Top Operations Jobs
The Process Manager will lead cross-functional teams in new assay launches and process improvement within the clinical testing sector. Responsibilities include stakeholder communication, project management, addressing project issues, and enhancing existing workflows while collaborating with engineering and product teams.
The Senior Process Manager will collaborate with various teams to support assay launches and process improvements in clinical testing. Responsibilities include managing project issues, reporting status, proposing workflows, and maintaining stakeholder communication on projects.
The Associate Director of Regulatory Affairs at Tempus will develop and implement regulatory strategies for medical devices. Responsibilities include leading submissions to regulatory authorities, ensuring compliance with various frameworks, and creating documentation needed for applications. The role entails collaboration with scientists, engineers, and legal teams, requiring strong leadership and project management skills.
Seeking a Senior Medical Science Liaison to support commercial, research, and educational objectives in oncology. Responsibilities include educating healthcare providers, organizing medical advisory boards, and providing scientific education. Requires advanced scientific or medical degree with KOL relationships in oncology.
The Sr. Manager, Commercial Learning & Development will develop and implement training programs for the sales teams, focusing on new hires and ongoing training. Responsibilities include coordinating training efforts, content creation, and providing feedback to sales management to enhance team performance.
The Research Operations Associate will manage key sites in the TIME clinical trials network, serve as the primary contact for research teams, draft and execute operational plans, collaborate with various teams, educate on clinical trial access, and oversee site support staff. Responsibilities include building client relationships, identifying resource gaps, and contributing to marketing and sales efforts.
The Associate Director will lead Translational Research projects, manage a team of computational scientists, design and implement research studies, analyze data, and provide actionable insights for biopharmaceutical partners. Responsibilities include project management, collaboration with stakeholders, and continuous improvement of research methodologies.
The Associate Director, Translational Research/Real-World Evidence will lead projects using Tempus' data to support biopharmaceutical partners. Responsibilities include managing a team, implementing computational strategies, collaborating with stakeholders, overseeing deliverables, and continuously improving research quality to support drug development decisions.
The Manager of Regulatory Affairs develops and leads regulatory strategies for medical devices, ensuring compliance with global regulatory authorities. This role involves submissions for FDA approvals, managing cross-functional teams, and aligning regulatory strategies with business objectives while maintaining communication with executive leadership.
The Director of Alliance Management is tasked with building partnerships with pharmaceutical companies to enhance their research using Tempus products. Responsibilities include managing data operations, providing scientific support, improving client satisfaction, and addressing partners' needs by developing customized proposals and cross-functional collaboration.
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