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Senior Clinical Data Manager
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Vforce Infotech
Edison, NJ (In Person)
$115,000 Salary, Full-Time
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Job Description
Senior Clinical Data Manager Vforce Infotech Edison, NJ Job Details Full-time | Contract $110,000 - $120,000 a year 16 hours ago Qualifications Data preprocessing Data compliance Regulatory compliance Analysis skills ICH guidelines Clinical research compliance Bachelor's degree Continuous improvement Attention to detail Query management Cross-functional collaboration Cross-functional communication Full Job Description Key Responsibilities Develop and maintain Data Management Plans (DMPs) across clinical studies Design Case Report Forms (CRFs) aligned with study protocols Configure and manage CRFs within Electronic Data Capture (EDC) systems Perform ongoing data cleaning, validation, and discrepancy management Generate, track, and resolve data queries; identify trends and inconsistencies Lead study-level database lock activities, including query closure and documentation review Conduct regular data review and reconciliation to maintain database integrity Partner with Clinical Operations, Biostatistics, and Regulatory teams to ensure data quality and compliance Provide data listings, reports, and study metrics to support clinical teams Build and maintain study trackers using Excel and/or Smartsheet to monitor progress and data quality Apply formulas, filters, and logic functions to ensure accuracy and visibility of study data Support process improvement initiatives to enhance data workflows and reporting Required Experience And Qualifications Bachelor's degree in Life Sciences or a related field 5+ years of experience in clinical data management, preferably in a medical device environment Hands-on experience with EDC systems and CRF configuration Strong knowledge of GCP, FDA, and ICH guidelines related to clinical data management Experience with data cleaning, query management, and database lock processes Strong analytical and problem-solving skills with high attention to detail Proficiency in Excel and/or Smartsheet for tracking and data organization Ability to work cross-functionally and manage multiple priorities in a fast-paced, start-up environment Preferred Qualifications Experience supporting cardiovascular or catheter-based medical device studies Familiarity with EDC configuration and ongoing system management (not initial build) Familiarity with data visualization tools (e.g., Power BI, Tableau, Spotfire, JMP) Experience supporting early feasibility or first-in-human studies What We're Looking For A hands-on data manager who takes ownership of data quality and keeps studies moving Strong attention to detail with the ability to identify inconsistencies and resolve issues proactively Comfortable working across multiple studies and shifting priorities in a fast-paced, start-up environment Able to work independently while collaborating closely with Clinical Operations, Biostatistics, and external partners Practical, execution-focused, and responsive to the needs of evolving clinical programs.