Search the 101 jobs at Precision Medicine Group

As a CQV Engineering Consultant, you'll lead client project initiatives in the life sciences sector, coordinating with various departments, developing technical documentation, mentoring team members, and supporting business development through networking and identifying client needs.

The Project Support Specialist at Precision for Medicine provides cross-functional support in managing clinical studies, including scheduling meetings, maintaining project timelines, managing training records, and communicating with study sites and team members. Responsibilities also include ordering supplies, preparing study binders, and supporting various project-related requests and documentation.

The Quality Assurance Specialist III is responsible for overseeing quality systems in a GxP laboratory setting, including internal and supplier audits, quality inspections, and handling non-conformances. The role involves data analysis for quality metrics, management of documentation, and supporting compliance across functions while leading projects and training initiatives.

The Project Support Specialist at Precision for Medicine supports project management by creating project timelines, scheduling meetings, managing study-related documentation, and maintaining training records. They will handle user access requests and supply orders, as well as prepare communications for study sites and assist with various project documentation tasks.

The Quality Assurance Specialist II will support GxP quality systems in a laboratory environment, conducting audits, managing document control, and ensuring product quality through inspection and release processes. They will also train personnel and participate in regulatory audits and quality improvements.

The Project Support Specialist provides cross-functional support in managing clinical studies, including maintaining project timelines, scheduling meetings, managing training records, and ensuring project compliance with regulatory guidance. They assist project leaders in document preparation, communication, and study material distribution.

The Project Support Specialist supports project management by creating timelines, scheduling meetings, maintaining study data, managing training records, and facilitating communications with team members and study sites.

The Project Support Specialist will provide cross-functional support to project teams, ensuring efficient management of clinical studies. Key responsibilities include maintaining project timelines, scheduling meetings, managing training records, and handling communications with team members and stakeholders. This role requires strong organizational skills and knowledge of clinical trial processes.

The Project Support Specialist will provide cross-functional support to manage clinical studies, including maintaining project timelines, scheduling meetings, managing data in Clinical Trial Management Systems, and facilitating communication among study teams.

The Project Support Specialist will support project teams through timelines, meeting coordination, document management, and database maintenance, contributing to clinical study management for precision medicine. Responsibilities include managing training records, creating project communication, and ensuring compliance with study protocols.

The In-House CRA II/Senior In-House CRA role involves supporting clinical research studies by recruiting study sites, managing documentation, ensuring compliance with guidelines, and acting as a contact point for the sites. Responsibilities include data entry oversight, facilitating communication between study teams and sites, and maintaining essential documents in compliance with regulatory requirements.

The UX Designer II collaborates with the Account Solutions team to design digital sales presentations and marketing materials. This role requires proficiency in design software, project management, and communication skills to execute projects effectively while adhering to design trends and principles.

As a Strategic Account Associate, you will support client relationships by preparing tactical plans, proposing ideas to enhance brand effectiveness, and mentorship. You will also interpret market and scientific data, promote new business opportunities, and contribute to company profitability while focusing on improving patient outcomes.

The Senior Feasibility Associate/Manager is responsible for managing and delivering feasibility projects, conducting pre and post-award feasibility analyses, providing insights during client meetings, and mentoring junior staff. This role is crucial in ensuring the effectiveness and efficiency of study planning, site identification, and supporting business development.

The Senior Feasibility Associate/Manager at Precision for Medicine will lead the management of feasibility projects, providing analysis and strategy for pre-award and post-award phases. Responsibilities include data-driven research, site identification, project leadership, and collaboration with cross-functional teams. The role also involves mentoring junior members and ensuring compliance with operational standards.

The Senior Feasibility Associate/Feasibility Manager at Precision for Medicine will manage pre and post-award feasibility projects and site identification, supporting study and business development teams. The role involves feasibility analysis, data-driven strategy development, and guiding project teams, while mentoring junior staff.

The Senior Feasibility Associate/Feasibility Manager will manage and deliver pre and post award feasibility projects, facilitate site identification, and provide analysis to support operational and business development teams. This role involves training junior staff and ensuring compliance with feasibility processes and standards.

The Senior Feasibility Associate/Manager will oversee pre and post-award feasibility projects, manage site identification, conduct data-driven analysis for study planning, and mentor junior staff. The role involves collaborating with various stakeholders and supporting business development efforts while ensuring quality and compliance with organizational standards.

The Senior Feasibility Associate/Manager will oversee the management of pre and post-award feasibility projects and site identification. This role entails supporting study teams with analytics and strategy, ensuring quality in deliverables, and guiding junior team members in their development. The associate will also actively engage with clients, providing insights and training to maintain operational excellence within feasibility departments.

The Senior Feasibility Associate/Manager will manage pre and post award feasibility projects, conduct feasibility analysis, support study teams, and engage in various growth-focused initiatives within the Feasibility Department at Precision for Medicine. Responsibilities include site identification, budget development, and providing training.