Search the 75 jobs at Precision For Medicine

The Senior Project Billing Analyst supports the Finance team with project billing responsibilities, financial reconciliations, invoicing, and maintaining project budgets. They liaise with clients, manage inquiries, maintain customer information, issue invoices, and assist in financial analyses. Attention to detail and strong relationship-building skills are essential.

The Principal Quality Assurance Auditor will oversee quality and compliance activities in clinical studies, serving as a subject matter expert, conducting audits, supporting regulatory inspections, and coordinating internal quality assessments. The role also involves developing SOPs, maintaining documentation, and implementing continuous improvement processes.

As a Senior Project Engineer, you will support clients in the engineering life cycle of advanced equipment and manufacturing processes, troubleshoot issues, align with various departments, and create technical documents. You'll leverage critical thinking to identify solutions and will engage in validation protocols following GxP practices.

As a Project Engineer, you will support and troubleshoot engineering processes for clients, facilitate project deliverables, create technical documentation, and execute validation protocols. This role requires travel and collaboration with various client departments in the life sciences sector to enhance operational excellence.

The Principal Scientist will oversee laboratory staff and lead bioanalytical and biomarker projects, including assay design and execution. Responsibilities include data analysis, improving procedures, troubleshooting assays, and collaborating with other teams, while also supervising staff and managing project expenses.

The Project Manager, Marketing Operations is responsible for leading marketing program execution, improving workflows, managing marketing systems, and providing insights to enhance efficiency. The role involves overseeing complex marketing campaigns, project management support, content management, and data analysis to drive strategic initiatives within the company.

The Project Support Specialist will contribute to the effective management of clinical studies by maintaining project timelines, organizing meetings, managing training records, overseeing study supplies and communications, and collaborating with project teams to ensure efficient operations.

The Project Support Specialist provides essential cross-functional support for managing clinical studies, including maintaining project timelines, coordinating meetings, managing training records, and ensuring study supplies are ordered and prepared. They serve as a critical communication point for project team members and external stakeholders while following regulatory guidelines.

The Project Support Specialist will provide cross-functional support for clinical studies, manage project timelines, schedule meetings, maintain documentation in CTMS, and ensure effective communication with study teams and stakeholders.

The Project Support Specialist will provide cross-functional support in managing clinical studies, creating and maintaining project timelines, scheduling meetings, managing study supplies, and supporting team leaders with various study reports and updates. Responsibilities include maintaining communication with study sites and investigators, and ensuring compliance with training and regulatory guidelines.

The Project Support Specialist will provide cross-functional support to manage clinical studies, including creating project timelines, scheduling meetings, managing training records, maintaining project documents, and communicating with study sites and team members.

The Project Support Specialist assists project teams by managing timelines, coordinating meetings, maintaining clinical trial documentation, and enhancing communication among team members and stakeholders. This role involves supporting study-specific training and user access management, as well as preparing study materials and reports under the guidance of project leadership.

As a CRA II at Precision for Medicine, you will be responsible for monitoring clinical studies, ensuring compliance with protocols and regulations, and coordinating study setup activities. Your role involves identifying investigators, preparing regulatory submissions, and managing travel commitments for site visits.

The Senior Data Engineer will implement, maintain, and monitor data standards for Precision for Medicine's laboratory services. Responsibilities include creating production-level code for biomarker data management, developing data processing pipelines, supporting data transfers, and collaborating with technical teams to ensure high-quality data delivery.

The Senior Software Engineer will lead the development and delivery of software products, manage business initiatives, design secure platforms, and ensure agile practices in a collaborative environment. Responsibilities include software solution planning, debugging, and lifecycle management.

As a Manager of Project Controls Engineering, you will collaborate with clients and team members to manage biomanufacturing projects, producing deliverables like budgets, project schedules, and cost reports. This role involves data analysis and maintaining project tools while fostering long-term client relationships.

As a Consultant in Project Controls Engineering, you will collaborate with clients and manage project controls for biomanufacturing projects, including generating budgets, schedules, risk analyses, and project reports. Your role will also involve analyzing project data and maintaining project management tools.

As a CQV Engineering Consultant, you will coordinate with client departments to support the engineering life cycle of equipment and processes, lead project initiatives, develop technical documentation, mentor team members, and support business development efforts.

The Project Engineer will align with various client departments to support engineering life cycles, authors technical documentation, execute validation protocols, and identify solutions to challenges. The role emphasizes creation of cross-functional relationships and contributing to a patient-focused mission.

The Quality Assurance Specialist III is responsible for maintaining GxP quality systems, conducting audits, managing quality events, and overseeing the release of materials and products in a laboratory setting. This role involves quality inspections, documentation, compliance activities, and collaboration across departments, as well as providing guidance to junior QA specialists.