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This role is for managing clinical research projects at Alimentiv, ensuring they meet timelines, budgets, and quality standards. You will coordinate with cross-functional teams and serve as the main contact for sponsors, contributing to the company's focus on advancing therapies for gastrointestinal diseases.
Alimentiv
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Alimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise, including supporting more than 70% of IBD compounds in development.
We operate as a private, profit-with-purpose company, channeling our commercial success back into scientific research, technology, and our people. With approximately 700 people across multiple countries and three service lines, we are growing deliberately, and the capability of our leaders and our organization is central to how we get there.
If you want to do meaningful work, build something real, and invest back in research that changes lives — we want to meet you!
In addition, as an Alimentiv Employee, you’re also eligible for the following programs:
Additional benefits may be available depending on the country of employment and are subject to local policies and eligibility.
To apply for this position, please submit your resume through the Alimentiv Careers Portal or via LinkedIn’s Easy Apply. Resumes must be submitted in English.
Lead the planning, execution, monitoring, and successful completion of assigned clinical research projects, ensuring delivery against timelines, budgets, quality standards, and project objectives.
Lead and coordinate cross-functional project teams, ensuring clear accountability, effective collaboration, and timely completion of project deliverables.
Serve as the primary point of contact for sponsors and clients throughout the project lifecycle, managing expectations, providing regular updates, and proactively resolving issues.
Oversee project activities to ensure compliance with applicable regulatory requirements, clinical research guidelines, and corporate policies.
Manage project documentation, tools, and resources, ensuring appropriate development, maintenance, and delivery of essential study materials and records.
Monitor project performance, identifying risks, addressing operational challenges, and implementing solutions to maintain project quality and timelines.
Coordinate key project activities, including site monitoring, data management, patient safety, statistical analysis, and final reporting, in collaboration with functional experts.
Support project planning and execution through effective stakeholder communication, project meetings, training, and vendor coordination as required.
Education/Experience: Bachelor's degree in a relevant discipline with 1–3 years of related experience, or a college diploma/degree with 4–6 years of related experience.
Alimentiv is aware of a continued increase in phishing scams, which use various methods of attack via email, text, voice and social media, including individuals posing as our recruiters and contacting candidates with fraudulent opportunities. Our hiring process always includes direct engagement with a recruiter or hiring manager, and we will never ask for sensitive personal information early in the process.
Official communication will only come from company email addresses containing "@alimentiv.com". If you are contacted about an open job at Alimentiv, please verify the domain of the sender's email address and confirm that you are being asked to apply on this website. If something doesn't feel right, we encourage you to verify before responding. If you believe you have been the victim of a phishing scam, please contact your local government cyber authority to report it.
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Alimentiv
