Clinical Data Manager

August 28

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Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management

201 - 500

Description

• Responsible for execution and adaptation of clinical data management plans and processes • Collaborate with multi-functional project teams and functional specialists • Regularly review quality of data output ensuring integrity, quality, validity, and reliability standards • Liaise with sponsors, sites, and project teams to address data issues and queries • Customize and/or adapt existing templates to define data management plan(s) • Collaborate with database developers, project leaders, and sponsors on database management • Regular communication with data collection sites and third-party service providers • Monitor the preparation, collection, documentation, and sign-off processes

Requirements

• Minimum of one to three years of related experience ideally in a clinical research environment • A minimum of a one-year post-secondary certification/diploma/degree in a relevant field of study • Knowledge of Statistical Analysis (SAS) testing and ICH-GCP guidelines • Skilled in the use of electronic database tools, systems, and coding dictionaries