Alimentiv

Responsible to plan manage organize evaluate and/or report on the day-to-day delivery of the Financial Planning & Analysis unit in collaboration with Sr. Director Financial Planning & Analysis. As part of the management in the department participate in the development and impl المزيد...

Transform Gastroenterology Research Through Advanced TechnologyAt Alimentiv were revolutionizing how inflammatory bowel disease and gastrointestinal therapeutics are developed and delivered to patients worldwide. As a leading gastroenterology-focused contract research organization we المزيد...

Support Project Management Regulatory and Contract and Legal in all site-related start-up activities. Establish relationships with study personnel at sites and act as main Alimentiv contact during site start-up. Prepare distribute and follow-up on start-up documents with sites. Plan a المزيد...

The eCOA Manager is responsible for the successful deployment and oversight of electronic Clinical Outcome Assessments (eCOA) solutions at Alimentiv including (but not limited to) electronic Patient Reported Outcome (ePRO) & eConsent collection. This role collaborates with interna المزيد...

Responsible for developing and leading high-quality strategic scalable software solutions that align with the companys goals and objectives. This role holds a strategic position within the software development lifecycle from planning to deployment and is key to shaping the technologic المزيد...

Transform Gastroenterology Research Through Advanced TechnologyAt Alimentiv were revolutionizing how inflammatory bowel disease and gastrointestinal therapeutics are developed and delivered to patients worldwide. As a leading gastroenterology-focused contract research organization we المزيد...

The Total Rewards Manager is responsible for the strategic design implementation and evaluation of total rewards programs across the organization including compensation benefits incentive programs and pay structures. This role ensures alignment with business objectives market competit المزيد...

Performs and coordinates all aspects of the clinical site monitoring services assessing for protocol and regulatory compliance. Responsibilities include driving investigative site and patient recruitment conducting source data verification assessing drug accountability data collection المزيد...

The Central Monitor (CM) will perform centralized and prompt monitoring activities for Phase I-IV clinical research and/or non-interventional studies (NIS) in accordance with project plans the protocol ICH-GCP and/or all applicable local and federal regulatory requirements as well as المزيد...

The Clinical Systems Specialist plays a critical role in the implementation management and optimization of clinical trial systems ensuring their functionality and alignment with study needs. They collaborate with the System Administrator & vendor on system configuration to deliver المزيد...

The Proposal Specialist will assist the BD team on the preparation of proposal responses associated with new business development opportunities and will work closely with the clinical subject matter experts to create customized comprehensive responses and budgets for Sponsors.Proposal المزيد...

Acts as the primary regional representative for the execution and delivery of clinical project(s); cultivate excellent Sponsor relationships provide project oversight assisting with project delivery services as required ensuring that projects are adequately and appropriately staffed m المزيد...

The eCOA Manager is responsible for the successful deployment and oversight of electronic Clinical Outcome Assessments (eCOA) solutions at Alimentiv including (but not limited to) electronic Patient Reported Outcome (ePRO) & eConsent collection. This role collaborates with interna المزيد...

Are you a seasoned ePRO expert looking to take ownership of a specialized function in a growing global organization Alimentiv is seeking an experienced ePRO Manager to lead the design implementation and oversight of electronic Patient Reported Outcomes (ePRO) systems in clinical trial المزيد...

Responsible to plan manage organize evaluate and/or report on the day delivery of the Clinical Monitoring unit. Role includes policy and process development and improvement product quality site and compliance monitoring staff resource planning and staff and contractor performance mana المزيد...

The Director of Monitoring and Site Management is responsible for overseeing the planning execution management and continuous improvement of clinical site monitoring activities. This position ensures the quality and compliance of clinical trials through effective site management monit المزيد...

The Proposal Specialist will assist the BD team on the preparation of proposal responses associated with new business development opportunities and will work closely with the clinical subject matter experts to create customized comprehensive responses and budgets for Sponsors.Proposal المزيد...

Responsible for developing and leading highquality strategic scalable software solutions that align with the companys goals and objectives. This role holds a strategic position within the software development lifecycle from planning to deployment and is key to shaping the technologica المزيد...

The MRI Technologist will play a significant role in ensuring the successful implementation and quality of Magnetic Resonance Imaging and/or Enterography (MRI/E) central reading services in clinical trials. This role will focus primarily on supporting the study team in determining cli المزيد...

As the primary sponsor liaison and advocate the Clinical Project Manager will plan execute manage and monitor regional single modality or therapeutic area clinical research projects. Utilizing existing templates processes and programs as a guide he or she will adapt/develop implement المزيد...