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The ERP System Administrator is an individual contributor role within Alimentiv’s Corporate Digital Enablement function, serving as the primary functional and technical owner of the Acumatica ERP platform that powers our Finance, Procurement, Logistics and Project accounting operations. Another si

Leverage your Acumatica expertise to elevate Alimentiv's operations. Join Alimentiv as an ERP Administrator specializing in Acumatica, where you will enhance finance and procurement workflows.

Alimentiv is seeking a seasoned medical writer to provide writing and consultation across regulatory documents such as protocols, ICFs, CSRs, and responses to regulatory authorities.

In this role you will be providing medical writing services and consultation to Clinical Research Scientists, Academic partners, Sponsors and/or the Corporation, which may include researching, writing, reviewing and editing scientific information, coordinating document reviews with authors, conducti

Alimentiv is seeking a seasoned medical writer to provide writing and consultation across regulatory documents such as protocols, ICFs, CSRs, and responses to regulatory authorities.

In this role you will be providing medical writing services and consultation to Clinical Research Scientists, Academic partners, Sponsors and/or the Corporation, which may include researching, writing, reviewing and editing scientific information, coordinating document reviews with authors, conducti

Alimentiv is seeking an ERP System Administrator to own and optimize the Acumatica ERP platform across Finance, Procurement, Logistics and Project accounting.

Configure and test procurement workflows aligned with Alimentiv’s project‑governed, goods & services‑based procurement model. Operate within Alimentiv’s gate‑based Finance Change Delivery Process; use JIRA as the system of record for change approval and evidence. The ERP System Administrat

Alimentiv is seeking an ERP System Administrator to own Acumatica administration and finance operations.

Responsible for the management of the Trial Master File (TMF) content and associated processes during the study life cycle from study setup to transfer/archiving.Work in partnership with study teams during periodic file reviews and audits to address findings related to the TMF.Manage access and orga