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As a Project Engineer, you will collaborate with clients in the life sciences sector, providing engineering support and troubleshooting for advanced manufacturing processes. You are responsible for authoring technical documents, executing validation protocols, and fostering cross-functional alignment to ensure project success while embodying a patient-focused mission.

The Manager Centralized Visit Report Reviewer leads and manages a team focused on ensuring the quality of clinical trial reports. The role involves mentoring, improving operational standards, providing strategic oversight, and ensuring compliance with regulatory requirements while fostering individual career development.

The Principal Statistical Programmer is responsible for performing all SAS programming tasks for clinical trial analysis and reporting. Responsibilities include collaborating across departments, developing and validating SAS programs for statistical analysis, creating randomization lists, and leading internal projects. The role also involves training, advising on programming techniques, and ensuring compliance with regulatory requirements.

The Lead Data Engineer oversees a team of data engineers in ensuring the implementation and maintenance of data standards for Precision for Medicine’s laboratory services. Responsibilities include leading projects, developing biomarker data management code, executing data processing pipelines, and collaborating with various stakeholders to guarantee high-quality data delivery.

The Feasibility Manager in the Precision for Medicine team oversees the management and delivery of various feasibility projects related to clinical trials. They conduct pre-award and post-award analyses, support business development efforts, and ensure the quality and accuracy of feasibility data and processes throughout the project lifecycle. The role involves collaboration with operational strategy teams and client interactions to support successful trial execution.

The Sr SAS Programmer at Precision for Medicine will develop and maintain SAS programming to support clinical data review, creating outputs like metrics and reconciliation reports. Responsibilities include validating SAS programs, ensuring timely project delivery, troubleshooting issues, participating in training, and contributing to SOPs. This role focuses on non-standard statistical programming related to clinical trials.

The Study Enrollment Lead coordinates and optimizes site recruitment strategies for clinical trials, supporting Clinical Research Associates (CRAs) through training and coaching. Responsibilities include developing site recruitment plans, ensuring effective communication with site staff, and collaborating with various teams to align recruitment efforts with study goals.