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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.