
201 - 500 employees
Founded 2020
🏥 Healthcare
đź’Ľ Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Alimentiv is a specialty contract research organization focused on gastrointestinal (GI) and liver diseases. With over 30 years of experience, Alimentiv offers a comprehensive range of clinical research and imaging services, including clinical trial management, site management, regulatory affairs, and precision medicine. The company is at the forefront of medical research and development, providing state-of-the-art imaging solutions and actionable biomarker insights. Alimentiv supports the development of GI compounds and is active in more than 60 countries, working with a network of medical and operational experts to accelerate clinical trials and patient recruitment.
🔥 19 hours ago
🇨🇦 Canada – Remote
đź’µ $61k - $102k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
đź‘» Ghost score 1%
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201 - 500 employees
Founded 2020
🏥 Healthcare
đź’Ľ Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Alimentiv is a specialty contract research organization focused on gastrointestinal (GI) and liver diseases. With over 30 years of experience, Alimentiv offers a comprehensive range of clinical research and imaging services, including clinical trial management, site management, regulatory affairs, and precision medicine. The company is at the forefront of medical research and development, providing state-of-the-art imaging solutions and actionable biomarker insights. Alimentiv supports the development of GI compounds and is active in more than 60 countries, working with a network of medical and operational experts to accelerate clinical trials and patient recruitment.
• Provide medical, scientific, and operational advice/support to Clinical Project Management, Data Management, and Medical Leadership teams for Central Image Management Solution (CIMS) clinical trials • Act as a point of contact for medical/scientific issues related to central reading with internal and external project teams • Interact with or escalate issues to Medical Leadership, Scientific Advisors/Collaborators, and Central Readers • Participate in internal, sponsor, project, and non-project-specific meetings and activities • Analyze and implement project-specific imaging requirements, quality control processes, and central reading paradigms • Lead development of project-specific Image Review Charters and Central Reader Variability Monitoring documentation where applicable • Develop CIMS project-specific documents, work instructions, process flows, and instruction manuals • Prepare and maintain site training materials related to imaging standards and scoring indices • Develop and review central reader training materials • Participate in central reader quality monitoring activities and trainings • Review central reading statistical data outputs and raw data to identify issues and trends • Develop mitigation strategies and process improvements related to central reading • Evaluate, implement, and support new imaging technologies and improved processes • Develop and maintain SOPs, work instructions, and associated central reading process documents • Participate in imaging modality-specific working groups and committees • Assist in developing and maintaining imaging and study-design standards • Contribute to continuous improvement through information sharing, training, and education
• Minimum of a Bachelor's Degree (specialization in Health/Life Sciences, Clinical Research or Medical Imaging preferred) • Strong analytical and problem-solving skills • Excellent learning agility and ability to work in ambiguity
• Bonus • Accommodations for job applicants with disabilities available upon request
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