Responsibilities :
Ensure data integrity on CRFs and other data collection tools and monitor for missing or implausible data.
Lead sample and data reconciliation efforts, resolving data queries with investigative sites, CROs, and internal lab operations in a timely manner.
Develop and enhance CRFs, CCGs, and data reconciliation processes.
Serve as the primary contact for clinical trial supplies vendors and oversee eTMF management with CROs.
Review site visit reports to ensure compliance with CRA qualifications.
Create and manage a training matrix, ensuring completion of necessary training for relevant roles.
Track and forecast study budgets.
Collaborate with internal teams to assess needs, resources, and project timelines.
Requirements :
At least 7 years of experience in data management within clinical trials or a related field.
Strong understanding of data collection, reconciliation, and reporting processes.
Experience managing interactions with vendors, CROs, and internal teams.
Ability to develop and implement process improvements and training programs.
Excellent organizational, communication, and problem-solving skills.
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