Alimentiv specializes in clinical trials and precision medicine, focusing on gastrointestinal disorders, building on a legacy of excellence in medical research since 1986.
London, Ontario
Industry-leading specialty GI contract research organization (CRO) transforming clinical trial outcomes and accelerating the development of life-changing therapies. We bring together deep GI expertise, advanced medical imaging solutions, clinical operation excellence and cutting-edge precision medicine/laboratory services. With a global network of 5,000+ sites in 60+ countries and growing, we expedite study activation and maximize patient enrollment, ensuring efficient and impactful clinical trials. Trusted by pharmaceutical and biotech partners, we support over 70% of all IBD compounds in development today – delivering customized end-to-end solutions to bring novel therapies to market. As a full-service CRO, our offering is tailored to meet your specific clinical research needs: • Clinical Trial Services • Medical Monitoring • Medical Imaging Solutions • Medical Research & Development • Medical Writing • Precision Medicine/Biomarkers • Clinical Pharmacology • Histopathology via Specialty Lab, AcelaBio • Spatial Biology • Statistics • Real-World Evidence Headquartered in London, Ontario, Alimentiv operates globally across Canada, the US, Europe, Asia-Pacific, and Latin America.
Remote · Toronto, Ontario, Canada
Apply biostatistical methods to support clinical trials through statistical planning, design, analysis, and reporting. Act as a subject matter expert providing guidance to project teams and contributing to the publication of scientific results.
Remote · Canada
Oversee financial activities, maintain accurate records, and ensure compliance with accounting standards and industry best practices. Responsibilities include managing month-end processes, account reconciliations, tax coordination, and implementing internal controls.
Remote · Toronto, Ontario, Canada
The role provides operational oversight of clinical projects, managing CRAs and investigator sites to ensure compliance with protocols and GCP guidelines. Key duties include developing monitoring plans, implementing recruitment strategies, and acting as the primary liaison between the monitoring team and the project team.
Remote · Canada
The role involves researching, writing, and editing regulatory documents such as protocols, investigator brochures, and clinical study reports. The candidate will also act as a project manager for writing deliverables and coordinate with external publication specialists.
Remote · Toronto, Ontario, Canada
Responsible for managing Trial Master File (TMF) content and processes from study setup through archiving. This includes ensuring inspection readiness, performing quality control reviews, and collaborating with study teams to address audit findings.
Remote · Canada
The ERP System Administrator serves as the primary functional and technical owner of the Acumatica platform, managing configuration, security, and finance operations. The role also focuses on optimizing procurement functionality and maintaining the SAP Concur-Acumatica integration via Celigo.
Remote · Toronto, Ontario, Canada
Apply biostatistical methods to support clinical trials through statistical planning, design, analysis, and reporting. Act as a subject matter expert providing guidance to project teams and contributing to the publication of scientific research.
Remote · Toronto, Ontario, Canada
Apply biostatistical methods to support clinical trials through statistical planning, design, analysis, and reporting. Act as a subject matter expert providing guidance to project teams and contributing to the publication of scientific results.
Remote · Toronto, Ontario, Canada
Manage Trial Master File (TMF) content and processes throughout the study lifecycle to ensure inspection readiness. Collaborate with study teams to perform file reviews, audits, and maintain the electronic file repository.
Remote · Toronto, Ontario, Canada
Oversees clinical operations and project deliverables, providing direct supervision and training to Clinical Research Associates (CRAs) and investigator sites. Acts as the primary liaison between the monitoring team and the clinical project team to ensure compliance with protocols and regulations.
Remote · Canada
The role involves providing medical writing and consultation services to create regulatory documents such as protocols, investigator brochures, and clinical study reports. The candidate will also act as a project manager for writing deliverables and coordinate with external publication specialists.
Remote · Canada
Oversee financial activities, maintain accurate records, and ensure compliance with accounting standards and industry best practices. Responsibilities include managing month-end processes, financial reporting, account reconciliations, and coordinating tax filings.
Remote · Canada
The ERP System Administrator serves as the primary functional and technical owner of the Acumatica platform, focusing on Finance, Procurement, and Logistics operations. Key duties include configuring system workflows, managing the SAP Concur integration via Celigo, and leading annual system upgrades.
On-site · London
Responsible for maintaining the quality, completeness, and compliance of Trial Master File documentation according to global regulatory standards. The role involves performing quality control checks, resolving documentation gaps, and ensuring inspection readiness through collaboration with cross-functional teams.
Remote · Canada
Oversee regional CRAs to ensure site compliance with study protocols, ICH-GCP, and local regulations. Manage site performance, lead monitoring activities, and serve as the primary operational liaison between sponsors and project teams.
Remote · Canada
The role involves providing medical writing and consultation services to create and edit regulatory documents such as protocols and clinical study reports. The candidate will also act as a project manager for writing deliverables and a liaison with external publication specialists.
Remote · Canada
The role involves providing medical writing and consultation services to create and edit regulatory documents such as protocols and clinical study reports. The candidate will act as a project manager for writing deliverables and coordinate with external publication specialists and internal scientists.
Remote · Canada
The role involves providing medical writing and consultation services to create and edit regulatory documents such as protocols and clinical study reports. The position also acts as a project manager for writing deliverables and a liaison with external publication specialists.
Remote · Canada
The role involves providing medical writing and consultation services to create regulatory documents such as protocols, investigator brochures, and clinical study reports. The writer will act as a project manager for deliverables, coordinating with authors and external publication specialists to ensure quality and compliance with industry standards.
Remote · Canada
The role involves providing medical writing and consultation services to create regulatory documents such as protocols, investigator brochures, and clinical study reports. The writer will act as a project manager for deliverables, coordinating with authors and external publication specialists to ensure quality and alignment with industry standards.
