Search the 30 jobs at Alimentiv

The Team Lead, Talent Acquisition will provide operational oversight and leadership for the talent acquisition team, managing full-cycle recruitment, optimizing service delivery, and enhancing staff engagement. They will also support employer branding efforts, liaise with stakeholders, and mentor team members while monitoring HR compliance and fostering a positive candidate experience.

The Sr. Accountant oversees financial activities, manages accurate financial records, ensures compliance with accounting standards, and supports the Sr. Manager, Accounting in project activities. Responsibilities include financial reporting, account reconciliation, payroll and taxation, process improvement, and team collaboration.

The Financial Planning & Analysis Coordinator will support financial planning and analysis activities, including forecasting revenue and costs, developing budgets, and analyzing project financial metrics. The role involves liaising between finance and operational teams, maintaining revenue models, and assisting with data collection for analysis. Strong communication and attention to detail are essential.

The Data Engineer will design, build, and maintain data pipelines and models while ensuring compliance with data governance requirements. Responsibilities include technical leadership on Azure, stakeholder engagement for data requirements, and promoting data capabilities across the organization. The role involves automation of data integration and continuous enhancement of data solutions and compliance with industry practices.

The Central Monitor will oversee monitoring activities for clinical research projects, ensuring compliance with protocols and regulatory requirements. They will analyze data to identify risks and data integrity issues, provide recommendations, and support project teams. Responsibilities include reviewing patient data, assessing site performance, documenting findings, and mentoring peers.

The Central Monitor will perform centralized monitoring for clinical studies, ensuring compliance with protocols and regulatory standards. Responsibilities include analyzing site and study data, assessing risks, and summarizing findings for project teams. The role requires proficiency in data analytics, strong analytical skills, and collaboration with other team members.

The Central Monitor will oversee monitoring activities for clinical research, ensuring patient safety and data integrity by analyzing data, identifying risks, and providing actionable recommendations. They will utilize analytical tools for reporting and escalate serious issues to project teams, while also supporting peers and contributing to process improvements within the organization.

The Central Monitor performs centralized monitoring for clinical research, ensuring safety and data integrity using statistical tools. Responsibilities include analyzing site data, identifying risks, developing action plans, and supporting project teams by summarizing findings and mentoring peers. The role requires collaboration, strong analytical skills, and adaptability to project needs.

The Central Monitor will perform monitoring activities for clinical research phases, ensuring patient safety and data integrity while analyzing site and study level data. Responsibilities include data review, risk assessment, issue escalation, and supporting project teams through reporting and documentation. The role requires strong analytical skills and proficiency in data analytics tools, alongside coaching and training team members.

The Azure Engineering Specialist is responsible for designing, deploying, and managing Azure infrastructure while working with development teams to ensure cloud integration and security. Responsibilities include optimizing performance, automating deployments, and collaborating with cross-functional teams to resolve technical issues.

The Country Manager oversees clinical trial operations, collaborating with global teams to ensure compliance with local regulations. Responsibilities include managing trial activities, leading regulatory submissions, vendor oversight, and maintaining key relationships within the region. The role requires strong project management skills and experience in clinical research across multiple phases.

The Country Manager oversees clinical trial operations within a specified country or region, ensuring compliance with regulations and managing trial logistics. Responsibilities include developing relationships with investigators, leading trial activities, vendor management, financial oversight, and leading regulatory submissions. The role demands strong project management skills and experience in phase 1-3 clinical trials.

The Country Manager will oversee clinical trial operations, ensure compliance with local regulations, lead project delivery, and manage vendor relationships. They will coordinate communications with study sponsors and integrate corporate operations functions while maintaining professional relationships with key regional stakeholders.

The Country Manager oversees clinical trials within a specific country or region, providing expertise in trial operations and managing regulatory compliance. Responsibilities include vendor management, leading operational activities, ensuring compliance with local regulations, and overseeing study communications and project management.

The Study Start Up Specialist supports project management and regulatory functions by coordinating site-related start-up activities, preparing necessary documentation, negotiating contracts, and maintaining site intelligence. This role involves acting as the primary contact for study sites to ensure timely execution and adherence to procedures, while developing relationships with study personnel.

The Study Start Up Specialist supports project management, regulatory and legal teams during site start-up activities, maintaining relationships with study personnel. They prepare and track site documents, negotiate contracts and budgets, and maintain intelligence on site metrics and timelines. This role involves providing reports, ensuring compliance, and assisting in project management tasks when necessary.

The Study Start Up Specialist will support project management, regulatory, and legal in site-related start-up activities. Responsibilities include preparing and following up on start-up documents, negotiating contracts, and maintaining a site intelligence tracker. The role involves acting as the main contact for study sites and collaborating with various teams to ensure timely start-up completion and compliance with local regulations.

The Study Start Up Specialist coordinates site-related start-up activities, prepares and manages required documentation, and ensures regulatory compliance. They act as the primary contact for study sites, facilitating timely completion of start-up tasks, budget negotiations, and tracking of site intelligence. The role involves close cooperation with project management and legal teams, requiring excellent communication skills and knowledge of clinical site requirements.

The Study Start Up Specialist is responsible for supporting site start-up processes by coordinating with project management, regulatory affairs, and contract/legal teams. They will prepare start-up documents, track activities, maintain relationships with sites, negotiate contracts and budgets, and provide reports related to study intelligence and metrics.

The Study Start Up Specialist supports site-related activities by managing start-up documents, tracking progress, and maintaining relationships with study sites. They work closely with Project Management, Regulatory, and Legal teams to ensure timely completion of required documentation and facilitate budget negotiations with site investigators.