Imaging Clinical Project Manager – 1-Year Limited Term

🔥 0 minutes ago

🇨🇦 Canada – Remote

💵 CA$89k - CA$148k / year

⏰ Full Time

🟢 Junior

🏥 Clinical Operations

👻 Ghost score 2%

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Alimentiv

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2020

🏥 Healthcare

💼 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.

📋 Description

• Act as the primary sponsor liaison and advocate throughout clinical research projects • Plan, execute, manage, monitor, and complete regional, single-modality, or therapeutic-area clinical research projects • Adapt or develop and implement project protocols, operational plans, risk management, resources, tools/materials, documents, and timelines • Manage day-to-day activities and performance of a multidisciplinary project team • Ensure decisions align with corporate, industry, sponsor, and regulatory requirements • Ensure project activities comply with applicable regulations, guidelines, and corporate policies • Maintain operational, financial, regulatory integrity, and safety • Develop or participate in project communications, training, regulatory submissions, audits, and third-party vendor selection • Manage creation, delivery, maintenance, and disposal of project data, documents, equipment, and tools • Prepare investigator updates and project-related reports • Assign and monitor interdisciplinary tasks including site monitoring, CRF and database development, data collection, patient safety/adverse-event management, document management, statistical analysis, final report writing, and publications • Ensure task completion meets quality, sponsor/client, project, and regulatory expectations • Address and resolve sponsor/client queries and issues • Plan and execute project meetings • Assist with site and patient recruitment strategies and materials • Assist with stakeholder training development • Provide regular project status and update reports to the sponsor/client

🎯 Requirements

• Minimum of one to three years of related work experience with ongoing training • Three-year College Advanced Diploma/Degree in a relevant field of study, preferably in (Health) Sciences or Clinical Research • Experience within Imaging is an asset • Strong communication skills • Strong attention to detail • Ability to understand the importance of building collaborative relationships • Ability to engage in continuous learning and self-development • Ability to continually foster teamwork

🏖️ Benefits

• Bonus • Home-based work • Occasional travel • Accommodations for job applicants with disabilities available upon request