expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet customer needs..., and/or a leadership role in a specific CDM task (e.g., Subject Matter Expert (SME). Comply with Good Clinical Practices (GCPs...
Lugar:
Buenos Aires | 02/08/2026 17:08:57 PM | Salario: S/. No Especificado | Empresa:
IQVIAWorldwideClinicalTrials d.o.o. is seeking a Records Management Compliance professional to manage TMF processes... data integrity across trials.Requirements include a university degree (life sciences preferred) and up to 1–2 years in TMF...
& Trial Lead for one or more clinicaltrials assuming responsibility for all CDS activities including selection... of all phases of clinicaltrials and ability to assess and determine study requirement from protocol reviewStrong Project and Risk...
WorldwideClinicalTrials is seeking an Associate I, TMF Operations to support TMF processing, review and archiving...
WorldwideClinicalTrials Limited is a general CRO seeking a Records Management Compliance Lead within the TMF...
WorldwideClinicalTrials Limited is a integral CRO seeking a Records Management Compliance Lead within the TMF...
WorldwideClinicalTrials is seeking an Associate I, TMF Operations to support TMF processing, review and archiving...
Lugar:
Mendoza | 02/08/2026 17:08:56 PM | Salario: S/. No Especificado | Empresa:
WorldwideWorldwideClinicalTrials is seeking a Team Lead, TMF Operations to maintain Trial Master Files readiness in line...
WorldwideClinicalTrials d.o.o. is seeking a Records Management Compliance professional to manage TMF processes... data integrity across trials.Requirements include a university degree (life sciences preferred) and up to 1–2 years in TMF...
WorldwideClinicalTrials d.o.o. is seeking a Records Management Compliance professional to manage TMF processes... data integrity across trials.Requirements include a university degree (life sciences preferred) and up to 1–2 years in TMF...