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The Consultant will create analytic plans, manage project timelines, run SQL queries, prepare quantitative slides, present insights to clients, mentor junior staff, and enhance knowledge of consulting methodologies in the pharmaceutical market.

The Document Control Specialist manages controlled documents within Precision for Medicine. Responsibilities include facilitating electronic document control processes, ensuring compliance and good documentation practices, assisting with document revisions, conducting training sessions, and supporting audits with documentation requests and preparation.

The Senior Project Billing Analyst supports the Finance team with project billing, financial reconciliation, invoicing, and revenue assurance. They manage customer contracts, maintain project budgets, resolve billing inquiries, and assist in preparing various financial reports while ensuring accuracy and adherence to timelines.

As a CRA II at Precision for Medicine, you will monitor and manage clinical studies, ensuring adherence to protocols and regulatory standards. You will coordinate investigative site activities, including setting up and overseeing studies, identifying researchers, and preparing necessary documentation. Your role will involve identifying risks and proposing solutions, with a focus on maintaining quality outcomes.

As a Senior Talent Acquisition Specialist, you will manage the full life cycle of recruiting, build talent communities, source candidates, facilitate interviews, and create recruitment branding materials. You will support hiring managers and develop strategies to attract top talent for hard-to-fill roles in a CRO setting.

The Data Engineer will support the Translational Data Services team by implementing and monitoring data standards, creating production-level source code for biomarker data management, executing quality control pipelines, and developing data transfer agreements. Collaboration with clients and various internal stakeholders is essential.

The Feasibility Manager leads pre-award and post-award feasibility projects, manages teams, conducts detailed feasibility analysis for clinical trials, and supports business development. Responsibilities include outreach for site identification and enrollment modeling, ensuring project deliverables meet timelines, and engaging with patient advocacy groups.