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The Mobile Site Vehicle Specialist supports clinical trials by managing mobile clinical sites, including logistics, supply management, and technical troubleshooting.
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The Employee Onboarding and Orientation Coordinator manages the onboarding process for new hires, ensuring a smooth transition and providing exceptional support, including coordinating paperwork and conducting orientation.
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The Director of Financial Operations oversees and optimizes financial processes, manages AP, AR, and Revenue operations, drives process improvements, and develops the financial operations team while ensuring compliance and alignment with business objectives.
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The Enterprise Performance Analytics Engineer builds and maintains data pipelines and models, ensuring data quality and efficient reporting for analytics teams.
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The Senior Associate, Operational Excellence will manage site operations, ensure regulatory compliance, lead staff development, and support business growth in clinical research.
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The Lifecycle Marketing Manager will develop and execute strategies to enhance patient engagement and retention through marketing automation, segmentation, and continuous testing.
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The Advisor, Talent Acquisition will enhance sourcing strategies and lead recruiting for PRN positions, mainly phlebotomists and RNs, while managing relationships with healthcare professionals and internal stakeholders.
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The Senior Software Engineer will develop full-stack applications using TypeScript, collaborate with designers, implement APIs, and ensure code quality in a remote setting.
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As a Specialist in Regulatory Operations, oversee compliance and regulatory activities for clinical trials, particularly for U.S. sites, ensuring adherence to FDA and global standards. Support IRB submissions and maintain essential regulatory documentation.
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The Growth Marketing Manager will optimize digital experiences, improve SEO performance, and drive conversions through technical implementation, data analysis, and collaboration across teams.
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The Specialist, Regulatory Operations oversees regulatory activities for clinical trials, ensuring compliance and supporting site operations. Responsibilities include managing IRB submissions, regulatory documentation, and collaborating with cross-functional teams.
