Provide administrative and processing support to project teams, including document management and meeting coordination. Act as the primary point of contact for project queries and ensure alignment with quality and regulatory standards.
Alimentiv
35 Remote Job Openings at Alimentiv
Manage and deliver full clinical site monitoring services, including the design and oversight of project monitoring, site recruitment, and regulatory filings. Act as a Lead CRA to mentor peers and serve as the primary liaison between the project team and sponsors.
Manage and perform full clinical site monitoring services, including the design and oversight of project monitoring, site recruitment, and regulatory filings. Act as a Lead CRA to mentor peers and serve as the primary liaison between the project team and sponsors.
Provide comprehensive administrative and clerical support to the Clinical Operations and Project Management department. Manage paper and electronic documentation, coordinate schedules, and assist with divisional supplies and budget expenses.
The role involves managing site-related start-up activities, including preparing document packages and coordinating with regulatory and legal teams. It also entails negotiating site budgets and contracts while maintaining intelligence trackers for study sites.
The specialist supports project management, regulatory, and legal teams in all site-related start-up activities for clinical studies. Key duties include managing start-up document packages, negotiating site contracts and budgets, and tracking site intelligence metrics.
Oversee financial activities, maintain accurate records, and ensure compliance with accounting standards and industry best practices. Responsibilities include financial reporting, account reconciliation, payroll, taxation, and implementing internal controls.
Manage and deliver full clinical site monitoring services, including the design and oversight of project monitoring, site recruitment, and regulatory filings. Act as a Lead CRA to mentor peers and serve as the primary liaison between the project team and sponsors.
Oversees clinical operations and project deliverables, providing leadership and oversight to Clinical Research Associates and investigator sites. Acts as the primary liaison between the monitoring team and the clinical project team to ensure protocol and regulatory compliance.
The Sr. TMF Lead provides expert oversight of Trial Master Files for complex programs to ensure quality, compliance, and continuous inspection readiness. This includes aligning sponsor requirements with CRO processes and mentoring TMF staff from study start-up through close-out.
Develop and manage standard reporting libraries and ad hoc analytical solutions to enhance clinical study data reporting. Analyze departmental operational metrics and support the integration of technical data reporting systems.
Develop and manage a standard library of reporting and analytical solutions to enhance clinical study data reporting. Analyze departmental operational and performance metrics to drive process improvement and optimize technical systems.
Apply biostatistical methods to support clinical trials through planning, analysis, and reporting while ensuring regulatory compliance. Lead and develop a team of statisticians and SAS programmers to deliver high-quality research results.
The role focuses on driving the adoption of AI tools by providing training, creating no-code prototypes, and translating technical capabilities into business workflows. It involves conducting needs assessments and establishing success metrics to measure the impact of AI initiatives.
Lead the day-to-day delivery of the Clinical Monitoring capability with a focus on European CRAs. Oversee resource planning, compliance, and the management of both internal staff and third-party contractors throughout the study lifecycle.
The Sr. TMF Lead provides expert oversight of Trial Master Files for complex programs to ensure quality, compliance, and continuous inspection readiness. This includes aligning sponsor requirements with CRO processes and mentoring TMF staff from study start-up through close-out.
Lead the day-to-day operational oversight of the Clinical Monitoring unit to ensure high-quality clinical trial execution. Manage staff, contractors, and third-party providers while partnering with sponsors and researchers to maintain regulatory compliance.
Lead and oversee the Clinical Monitoring unit to ensure high-quality execution of global clinical trials. Manage staff, contractors, and third-party providers while partnering with sponsors to maintain regulatory compliance and operational excellence.
The Business Development Director is responsible for achieving annual sales targets and expanding the client base within the Eastern US and Canada region. This includes leading proposal development, managing client relationships, and coordinating with cross-functional teams for bid defenses and contract negotiations.
Drive growth and expand partnerships within the North American East Coast region through strategic sales and new business development. Manage the full client lifecycle from proposal development and bid defenses to contract negotiations and ongoing relationship management.
Provide strategic and operational leadership over the accounting function, ensuring the integrity and accuracy of all financial reporting. Oversee the full accounting cycle, ERP system ownership, tax compliance, and the management of payables and receivables.
Responsible for the administration, configuration, and operational delivery of the Veeva Vault Clinical platform, including eTMF and CTMS. The role involves managing system security, compliance, user enablement, and supervising a team of solution delivery staff.
Lead the global delivery of full-service clinical trials by providing strategic oversight to project management and finance teams. Drive organizational strategy, process optimization, and operational performance while acting as a trusted partner to sponsors and clients.
The role involves planning and evaluating global quality assurance services, including conducting internal and vendor audits. It also requires developing quality system documents and ensuring compliance with regulatory trial conduct standards.
Support financial planning and analysis activities, including revenue forecasting, profitability analysis, and budget development across product lines. Act as a liaison between finance and operational groups to track project financial metrics and identify cost-saving opportunities.
Manage and deliver full clinical site monitoring services, including the design and oversight of project monitoring, site recruitment, and regulatory filings. Act as a Lead CRA to mentor peers and serve as the primary liaison between the project team and sponsors.
Imaging Research and Development Associate (1-year contract)
Alimentiv
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Full Time
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2 months ago
Alimentiv
The associate will provide medical, scientific, and operational support for clinical trials, acting as a point of contact for central reading processes. They will collaborate with internal and external stakeholders to develop project-specific documentation, training materials, and quality monitoring strategies.
The Statistician will apply biostatistical methods to support clinical trials, including statistical planning, design, analysis, and reporting. They will also act as a subject matter expert, providing guidance to project teams and stakeholders while ensuring compliance with regulatory standards.
The Statistician will apply biostatistical methods to support clinical trials, including statistical planning, design, analysis, and reporting. They will act as a subject matter expert, providing guidance to project teams and stakeholders while ensuring compliance with regulatory standards.
The role involves planning, managing, and evaluating the delivery of the Clinical Monitoring unit while ensuring compliance with regulatory requirements. It also includes managing team performance and collaborating with internal and external partners to improve service delivery.
The Workplace AI Specialist supports the adoption of AI tools by providing training and implementation support to staff. They act as a liaison between technology teams and end users, translating technical capabilities into accessible resources.
This role involves managing, delivering, and performing full clinical site monitoring services for projects, which includes overseeing training, recruitment, data management, budget monitoring, and regulatory filings according to SOPs and GCP best practices. As a Lead CRA, the individual will act as the primary liaison between CRAs and the project team, potentially participating in the development of project plans and protocols.
This role is responsible for building leadership bench strength and organizational capabilities by designing and leading leadership development programs for various levels and translating talent insights into actionable development pathways. The manager will also lead organizational capability initiatives in critical areas like communication and AI fluency, while supervising a small team of learning professionals.
This role supports clinical site monitoring services both in-house and remotely, focusing on ensuring compliance with protocols, SOPs, and regulatory guidelines for full-service studies. Key duties include site management activities to drive patient recruitment, remote data review, query resolution, and oversight of compliance documentation.
The Clinical Project Manager will plan, execute, manage, and monitor clinical research projects, adapting and implementing operational plans, risk management, and timelines while ensuring alignment with all corporate and regulatory requirements. This role involves managing the day-to-day activities of a multidisciplinary team, overseeing tasks from site monitoring and CRF development to statistical analysis and final report writing.
