Résultats de recherche

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

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

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.

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

Serve as the primary Acumatica administrator across the Alimentiv instance: configuration, user access, security, workflows, and module settings. Configure and test procurement workflows aligned with Alimentiv’s project‑governed, goods & services‑based procurement model. Operate within Aliment

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

Alimentiv is a global Contract Research Organization (CRO) with a clear and focused strategy: advancing therapies for gastrointestinal (GI) diseases. For accounting and finance professionals, Alimentiv offers the opportunity to contribute to a business where financial stewardship, transparency, and

A leading clinical research organization in Canada is seeking a TMF Coordinator to manage Trial Master File processes throughout the study lifecycle.The ideal candidate will have a college diploma and 1-3 years of relevant experience, emphasizing TMF organization and regulatory compliance.Responsibi