Configuration Specialist II
2 days ago
require leading special projects and ensuring deliverables are met in accordance with project schedules.
DESCRIPTION
Serve as an advanced member of the Configuration Team and work with cross-functional teams on the implementation of new and existing client projects
Work to become an expert in Trial Interactive features and functionality including Global Learn (LMS)
Manage external and internal documentation such as work instructions, QC checklists and knowledge base entries
Configure application settings in Trial Interactive as per project requirements and execute quality control measures to ensure client and project expectations are met
Produce high quality deliverables and ensure junior members of the team are properly trained in addition to providing oversight and mentorship
Assist Technical Services and Project Mangers in fulfilling client expectations as it relates to TI application configurations
Perform other special projects or duties when required such as validation and UAT script execution and participating in integration projects to understand the impact on TI application settings
Complete all other tasks that are deemed appropriate for this role and assigned by the manager/supervisor
REQUIRED SKILLS
Knowledge of various technological concepts
Hands-on knowledge of the Trial Interactive product suite, with a concentration in Study Start Up (SSU), Electronic Trial Master File (eTMF), Collaborative Workspace, and Content Management System
Knowledge of clinical development phases and processes
Superior written and spoken communication skills in English
Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook)
REQUIRED EXPERIENCE AND QUALIFICATIONS
Minimum Bachelor’s degree or its equivalent in work experience
Minimum 6 months – 4 years of experience in the IT and/or Life Sciences industry
Experience with rolling out technological initiatives in a collaborative environment
DESIRED SKILLS AND EXPERIENCE
Practical experience in the Life Sciences industry (pharmaceutical, biotechnology or CRO experience preferred) such as management of eTMF and understanding of the DIA reference model
Knowledge of technology within the industry
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