Our Clinical Project Directors, Project Managers, Coordinators, and Specialists are experienced professionals trained to deliver superior service to our clients. Their collaborative approach, combined with deep therapeutic expertise and exceptional organizational and interpersonal skills, creates a responsive, client-driven framework for success.
Our full suite of imaging modalities includes endoscopy, digital pathology, magnetic resonance, and intestinal ultrasound, each of which can be customized to meet the specific requirements of your trial.
Our team of experts can guide you through the entire imaging process, from trial design and protocol development to study execution and closeout.
Let us help you achieve success in your clinical trial with our innovative and reliable imaging solutions. Contact our business development team today to learn more about how Alimentiv can support your study.
Early feasibility assessment is a complex but valuable process, employing Alimentiv’s expert insights (medical, operations, bio stats, regulatory, laboratory) to significantly heighten the reliability of planning decisions for your clinical study.
Alimentiv’s multi-disciplinary team of experts provides scientific, statistical and safety assessment of your proposed study and delivers recommendations that improve your protocol and optimize site selection, patient recruitment, patient safety and study timeline decision.
At Alimentiv, we leverage our long-standing global network of top-tier GI investigators to identify, qualify and select the sites that can achieve recruitment goals and deliver high-quality data for your study.
We know what it takes to implement GI studies that deliver quality results. Assessing study risks, optimizing protocol design, selecting the appropriate countries, sites and patient population are key to achieving your project goals. With our experience over the past 34 years, managing more than 150 studies in over 60 countries, Alimentiv is well-positioned to assist in setting your study up for success.
Our Project Managers have extensive experience planning all facets of clinical trials during study start-up activities. Utilizing proven methodologies and existing templates, all planning activities are meticulously tailored to meet Sponsor needs to ensure seamless management of clinical studies.
As part of our innovative Risk Based Quality Management approach, we establish study risks in the early stages of the clinical trial by gathering risk information from cross-functional leads to establish a comprehensive risk registry.
The risk registry is then used to inform trial planning including:
Our holistic approach drives proactive study planning in each functional area of the study team.
Critical risk mitigations are identified by ensuring cross-functional leads and participating in risk identification activities in the early phase of the clinical trial to safeguard the quality of the trial and the safety of the participants.
At Alimentiv, we pride ourselves on our years of IBD as well as our longstanding global relationships with IBD professionals. Using comprehensive recruitment models and templates during start-up and throughout the life of a clinical trial, we leverage our expertise to work with sites on realistic and achievable recruitment plans based on proven strategies that ensure successful recruitment.
At Alimentiv, we employ the use of established recruitment models to serve as the basis of our recruitment strategy. We create recruitment models that deliver by coupling our strategies with customized features based on Sponsor requirements.
A robust project plan is based on comprehensive understanding of study requirements established in the early stages of the study planning phase. Applying our expertise with industry-standard project management methodologies, we work closely with the sponsor to design project plans that meet the unique needs of their study.
Clinical Study Management (CSM) is responsible for the coordination of all activities from all functional groups contracted for a project. They serve as the central portal for communication flow and accountability for the completion of tasks across the project. CSM will coordinate overall study timelines and manage these as the study progresses.
As the primary point of accountability for end-to-end study delivery CSM provides ongoing review and management of project plans and Work Instructions, risk assessments, mitigations, training needs, timelines, contracts and study resources.
We have capable leaders who partner with empowered cross-functional teams to establish clear accountability for assigned tasks.
Ongoing monitoring of study activities using a standard suite of tools and systems. Production of ongoing study status reports customized to client needs.
Experienced with all vendor types required to conduct a trial, including IXRS to county-level depots, PRO providers and central laboratories.
Vendor oversight is based on clear service level agreements and Key Performance Indicators.
FAQ documents, medical representation at study meetings, tracking in an e-training system for Alimentiv staff, and managing compliance of all assigned team members to the training plan.
Effective and timely communication is critical to achieving study objectives. We pride ourselves in our ability to build strong, transparent communication channels with our clients, study team, vendors and other stakeholders. We agree to clear guidelines upfront for how the information will be shared, as well as who’s responsible for and needs to be looped in on each project communication. Alimentiv provides a commitment to strategic and innovative thinking in partnership with clients for oversight, recruitment strategies, management of risk, and quality.
In-house services or in collaboration with client or vendor, including Investigator Meeting planning & management, vendor and site payments, and provision of study supplies.
Risk Based Quality Management (RBQM) approach to monitoring off-site activity, supported by a Project Management and Monitoring team experienced in IBD.
Measure performance to contract. Management of ongoing tasks, identifying timeline drift, out-of-scope activities, and change order management.
Comprehensive oversight of all functional tasks and their interrelatedness. Ensuring accountability for tasks and timely completion. Measure performance to contract.
Measure performance to contract. Management of ongoing Reviews Managing DMC, DSMB or SSC to deliver key data that enable downstream decisions for clients.
Alimentiv is committed to delivering quality clinical research services in a professional, efficient, timely, and cost-effective manner while protecting patient safety and data integrity for regulatory submissions. We do this using a Quality Management System (QMS) designed to meet applicable global regulatory, technical and organizational requirements, as well as industry standards.
Alimentiv’s TMF Operations team produces a Trial Master File that supports the science behind the study.
We know the TMF is critical in demonstrating subject safety and data integrity throughout the study lifecycle. Alimentiv is a proud partner of Veeva Vault eTMF to deliver top-end active TMF management. Our TMF framework is structured using the guidelines and standards set forth by ICH-GCP and global regulatory agencies and the TMF reference model. We go beyond the basics to ensure your TMF is a cohesive, inspection-ready study package.
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