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Alimentiv

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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

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Pharmaceutical Manufacturing
501–1,000 people

About

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.

Open positions

Intermediate Full-Stack Software Developer

Remote · Calgary, Alberta, Canada, Edmonton, Alberta, Canada, Halifax, Nova Scotia, Canada, Kingston, Ontario, Canada, London, Ontario, Canada, Montreal, Quebec, Canada, Ottawa, Ontario, Canada, Regina, Saskatchewan, Canada, Toronto, Ontario, Canad…

The developer will manage the software development lifecycle from design to implementation, focusing on imaging products and cross-functional collaboration. Responsibilities also include providing technical support, performing code reviews, and authoring comprehensive technical documentation.

TMF Associate

Remote · London, Ontario, Canada

Responsible for managing Trial Master File (TMF) content and processes from study setup through archiving to ensure inspection readiness. This includes performing periodic file reviews, managing electronic repositories, and collaborating with cross-functional teams to address audit findings.

Sr. Clinical Operations Lead (Clinical Trial Manager)

Remote · London, 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.

TMF Coordinator

Remote · London, Ontario, Canada

The TMF Coordinator is responsible for maintaining the quality, completeness, and compliance of Trial Master File documentation according to global regulatory standards. This includes performing quality control checks, managing eTMF systems, and collaborating with cross-functional teams to ensure inspection readiness.

TMF Coordinator

Remote · Vancouver, British Columbia, Canada

The TMF Coordinator is responsible for maintaining the quality, completeness, and compliance of Trial Master File documentation according to global regulatory standards. This includes performing quality control checks, managing eTMF systems, and collaborating with cross-functional stakeholders to ensure inspection readiness.

TMF Coordinator

Remote · Windsor, Ontario, Canada

Maintain the quality, completeness, and compliance of Trial Master File documentation in accordance with global regulatory standards. Collaborate with cross-functional stakeholders to ensure TMF content is inspection-ready and supports clinical trial execution.

TMF Coordinator

Remote · Kingston, Ontario, Canada

The TMF Coordinator is responsible for maintaining the quality, completeness, and compliance of Trial Master File documentation according to global regulatory standards. This includes performing quality control checks, managing eTMF systems, and collaborating with cross-functional stakeholders to ensure inspection readiness.

TMF Coordinator

Remote · Kitchener, Ontario, Canada

The TMF Coordinator is responsible for maintaining the quality, completeness, and compliance of Trial Master File documentation according to global regulatory standards. This includes performing quality control checks, managing eTMF systems, and collaborating with cross-functional teams to ensure inspection readiness.

TMF Coordinator

Remote · Ottawa, Ontario, Canada

The TMF Coordinator is responsible for maintaining the quality, completeness, and compliance of Trial Master File documentation according to global regulatory standards. This includes performing quality control checks, managing eTMF systems, and collaborating with cross-functional teams to ensure inspection readiness.

TMF Coordinator

Hybrid · Kingston

The TMF Coordinator is responsible for maintaining the quality, completeness, and compliance of Trial Master File documentation in accordance with global regulatory standards. They will perform quality control checks, manage document indexing, and collaborate with cross-functional teams to ensure inspection readiness.

Imaging Clinical Project Manager (1 -Year Limited Term)

Remote · Halifax, Nova Scotia, Canada

The Clinical Project Manager plans and executes regional clinical research projects while serving as the primary liaison for sponsors. They are responsible for managing multidisciplinary teams, ensuring regulatory compliance, and overseeing project timelines and documentation.

Imaging Clinical Project Manager (1 -Year Limited Term)

Remote · Calgary, Alberta, Canada

The Clinical Project Manager plans and executes regional clinical research projects while serving as the primary liaison for sponsors. They manage multidisciplinary teams to ensure project protocols, timelines, and regulatory requirements are met throughout the project life cycle.

Imaging Clinical Project Manager (1 -Year Limited Term)

Remote · London, Ontario, Canada

The Clinical Project Manager plans and executes regional clinical research projects, serving as the primary liaison for sponsors. They manage multidisciplinary teams to ensure project protocols, timelines, and regulatory requirements are met.

Imaging Clinical Project Manager (1 -Year Limited Term)

Remote · Kingston, Ontario, Canada

The Clinical Project Manager plans and executes regional clinical research projects while serving as the primary liaison for sponsors. They manage multidisciplinary teams to ensure project protocols, timelines, and regulatory requirements are met.

Imaging Clinical Project Manager (1 -Year Limited Term)

Remote · Montreal, Quebec, Canada

The Clinical Project Manager plans and executes regional clinical research projects while serving as the primary liaison for sponsors. They are responsible for managing multidisciplinary teams, ensuring regulatory compliance, and overseeing project timelines and documentation.

Imaging Clinical Project Manager (1 -Year Limited Term)

Remote · Edmonton, Alberta, Canada

The Clinical Project Manager plans and executes regional clinical research projects while serving as the primary liaison for sponsors. They manage multidisciplinary teams to ensure project protocols, regulatory requirements, and timelines are strictly followed.

Imaging Clinical Project Manager (1 -Year Limited Term)

Remote · Kitchener, Ontario, Canada

The Clinical Project Manager plans and executes regional clinical research projects while serving as the primary liaison for sponsors. They manage multidisciplinary teams to ensure project protocols, timelines, and regulatory requirements are met.

Imaging Clinical Project Manager (1 -Year Limited Term)

Remote · Calgary, Alberta, Canada, Edmonton, Alberta, Canada, Halifax, Nova Scotia, Canada, Kingston, Ontario, Canada, Kitchener, Ontario, Canada, London, Ontario, Canada, Montreal, Quebec, Canada, Ottawa, Ontario, Canada, Quebec, Quebec, Canada, S…

The Clinical Project Manager will plan, execute, and monitor clinical research projects while acting as the primary liaison for sponsors. They are responsible for managing multidisciplinary teams, ensuring regulatory compliance, and overseeing project timelines, budgets, and documentation.

Statistician

Remote · London, Ontario, Canada

Apply biostatistical methods to support clinical trials, including statistical planning, analysis, and reporting throughout the project life cycle. Provide subject matter expertise to project teams and contribute to the publication of scientific research data.

Statistician

Remote · Victoria, British Columbia, 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.