Sr/Clinical Data Team Lead, cFSP
メキシコシティ, メキシコ合衆国
Job Description
Job Overview
Manage the end-to-end delivery of data management services for single or multi-service projects with minimal guidance, ensuring quality deliverables are provided on time and within budget to meet customer satisfaction. Provide comprehensive data management expertise to the Data Management (DM) team, ensuring high-quality data management products that meet customer needs. Lead the team in project planning, execution, and close-out, oversee financial management for data management activities, and ensure effective communication and milestone deliverables. Perform the role of Data Team Lead (DTL).
Essential Functions
Gather study setup requirements through discussions and communication with relevant stakeholders.
Support and oversee the validation of new device integrations with minimal guidance.
Perform regular data cleaning activities to ensure clean data and timely deliverables to sponsors.
Ensure all deliverables meet expected quality standards and customer expectations.
Ensure service and quality meet agreed-upon timelines and deliverables in the contract/Scope of Work (SOW) with guidance.
Support the training of new joiners.
Lead internal study meetings, internal/sponsor audits, and participate in study kick-off meetings and other sponsor meetings.
Track and manage projects, oversee project progress, identify risks, and take corrective action as required.
Manage and oversee the implementation of new technology/database revisions with guidance.
Work closely with the programming team for process innovation and automation.
Comply with training and eSOP reading requirements.
Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
Collaborate effectively with the Line Manager and other team members across functions.
Perform other duties as directed by the Line Manager.
Qualifications
Bachelor's Degree in Pharmacy or an equivalent field preferred.
4 years of direct Data Management experience, including a minimum of 1 year as a CDM project lead preferred.
Fluency in spoken and advanced written English.
Advanced skills in computer applications such as Microsoft Excel, Word, and Inbox.
Advanced understanding of the drug development lifecycle and overall clinical research process.
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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
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