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 · Canada
Conduct site management through remote and onsite visits to ensure compliance with SOPs, protocols, and GCP. Responsibilities include data review, TMF documentation maintenance, and providing operational support or mentorship depending on seniority level.
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.
Remote · London, Ontario, Canada, Toronto, Ontario, Canada
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.