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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.
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 Project Controls Engineer will support cross-functional client departments, provide troubleshooting assistance, create project deliverables including budget estimates and risk analysis, and help maintain the organization's Patient Focused and People First mission. Responsibilities also include establishing strong relationships and proactively identifying solutions for project roadblocks.
The Senior Manager of Site Contract Management leads the Site Contracts team, establishing processes and overseeing all aspects of contract management. The role involves managing resources, reviewing and negotiating agreements related to clinical trials, ensuring adherence to standards, and representing the organization in various meetings.
As a Project Controls Engineering Consultant, you will collaborate with clients and teams to support biomanufacturing projects, delivering project controls deliverables such as budgets, schedules, risk analyses, and cost reports. You will analyze complex data and ensure project alignment across various departments, while also maintaining internal tools and dashboards.
As a Consultant in Project Controls Engineering, you will collaborate with various teams to support biomanufacturing projects, create project budgets, schedules, and reports, analyze project data, and facilitate clear communication for decision making. You will also be responsible for maintaining internal project management tools and fostering long-term client relationships.
Project Farma seeks talented professionals in various roles including Project Engineers, Consultants, Managers, and Directors in the life sciences industry, focusing on advanced therapies, project management, and operations support.
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