Precision Medicine Group
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Jobs at Precision Medicine Group
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Join the Talent Community at Precision Medicine Group to express your interest in potential career opportunities. This is not an official application but allows you to connect with recruiters by sharing your contact information and career interests, and adding a resume for future openings.
The Quality Assurance Specialist II supports regulated systems in a GxP laboratory environment, focusing on quality control, internal audits, and document management. Responsibilities include managing non-conformances, customer complaints, CAPA processes, and conducting internal audits, along with supporting daily operations and process observations.
This position is responsible for financial planning and analysis, strategic planning, management reporting, decision support, and controls. The role involves collaborating with senior management, preparing budgets, forecasts, and reports, and providing insights to drive business growth initiatives.
Develop client focused budgets and proposals for Phase I-IV clinical trials. Coordinate RFP responses and collaborate with operational teams. Support Work Order and RFI deliverables as needed.
The SaaS Implementation Consultant is responsible for managing the implementation of products, leading discussions on configuration requirements, setting up automated workflows, troubleshooting integrations, and training clients on best practices. They will act as a technical expert in customer data and contribute to product advancements while mentoring junior team members.
The Sr. Accountant is responsible for maintaining the general ledger, managing cash applications, inter-company invoicing, and ensuring timely financial reporting. This role supports daily banking operations, processes payables and receivables, and collaborates across departments to meet financial goals while adhering to regulations.
The Senior Talent Acquisition Specialist at Precision for Medicine is responsible for full life cycle recruiting, building talent communities, sourcing candidates, facilitating the interview process, and developing recruiting strategies. Preferred candidate from Poland or Hungary.
The Senior Talent Acquisition Specialist at Precision for Medicine is responsible for full life cycle recruiting, building talent communities, sourcing candidates, and facilitating the interview process. The role requires a Bachelor's degree and 5+ years of recruiting experience in a CRO setting. Preferred candidate based in Poland or Hungary.
The Manager, Centralized Visit Report Reviewer leads and manages a team of Clinical Visit Report Reviewers to maintain quality standards, ensure compliance with regulations, and achieve performance goals. Responsibilities include mentoring team members, collaborating on operational improvements, and providing strategic oversight and support to optimize report management processes.
The Senior Statistical Programmer will support and lead SAS programming efforts for clinical studies, including developing, testing, and documenting SAS programs. The role requires interaction with clients and mentoring junior team members while ensuring adherence to project scope and budget.
As a Senior Statistical Programmer, you will support and lead SAS programming efforts for clinical studies, ensuring compliance with industry standards. You will develop, validate, and document SAS programs, create specifications for datasets, and collaborate with clients while providing guidance to junior team members.
The Manager, Site Start-up oversees the daily activities of Regulatory and Start-up Specialists, ensuring compliance with SOPs and quality standards. They manage personnel development, coordinate inter-departmental communication, address project issues, and contribute to training and resource allocation for site start-up projects.
The Managing Counsel provides legal support for client and vendor contracts, negotiating agreements, advising business teams, researching legal risks, and ensuring compliance with company and legal standards. They also maintain contract management systems and facilitate the contracting process.
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.
The Manager, Site Start Up will oversee daily activities of Site Start Up personnel, ensuring compliance with SOPs and regulatory requirements. Responsibilities include mentoring staff, managing resources, conducting performance reviews, and enhancing communication and training processes within the team.
The Senior Research Scientist will oversee and conduct systematic literature reviews and quantitative evidence synthesis studies, develop client-ready deliverables, manage project components, ensure timely delivery, and mentor junior staff while contributing to proposals and presentations.
The Senior Project Controls Engineer is responsible for managing project controls deliverables, collaborating with cross-functional teams, and providing hands-on support in navigating engineering processes. Duties include producing budget estimates, detailed project schedules, cost reports, and risk assessments while fostering relationships with clients and promoting the organization's mission.
The Principal Quality Assurance Auditor oversees quality and compliance for clinical studies, serving as a subject matter expert. Responsibilities include auditing, supporting quality management systems, conducting training, and ensuring adherence to regulations. They also manage documentation and collaborate on audits for vendors and sites, with a focus on improving compliance and quality systems.
The Senior Project Controls Engineer will support clients in navigating the engineering life cycle, generate high-quality project deliverables, and provide hands-on troubleshooting. Responsibilities include creating budgets, managing project schedules, conducting feasibility analyses, and producing project reports while fostering key relationships with internal and external stakeholders.
The Project Engineer will align with various client departments, provide support for engineering processes, author technical documents, execute validation protocols, and build relationships to enhance client services while promoting a patient-focused environment.