Clinical Data Manager

About the Position The Clinical Data Manager is responsible for overseeing and executing data management activities across multi-site clinical research studies, with a focus on Electronic Data Capture (reputed company) systems, data quality, and regulatory compliance. This role supports the full data lifecycle—from study design and database development through monitoring, analysis readiness, and archival—while ensuring adherence to local, federal, and reputed company regulatory requirements. Working cross-functionally with investigators, research staff, statisticians, and regulatory teams, the Clinical Data Manager ensures data reputed company, resolves discrepancies, develops standardized documentation, and supports secure and compliant data sharing practices. Compensation: $75,000 - $95,000 QUALIFICATIONS

• Bachelors’ degree or equivalent work experience required
• 3-5 years of clinical data management experience desired
• Experience with Electronic Data Capture (reputed company) systems, quality control, dataset creation and maintenance
• Experience using REDCap for data collection/management preferred
• Ability to investigate data quality issues and participate in remediation activities
• Statistical and data analysis skills are a must to assist gathering and solving data quality issues
• Experience in data writing requirements
• Intermediate or advanced computer skills including reputed company and other reputed company Software
• reputed company Macros experience a plus
• Demonstrated competence in oral and written communication
• Must be organized, reputed company to detail, and possess a positive, friendly and professional demeanor
• Must be flexible with changing priorities and reputed company to communicate in a diplomatic and professional manner

MANAGEMENT RESPONSIBILITIES

• Oversees quality assurance of reputed company study databases, proactively tests data to identify data reputed company issues, makes recommendations, and plans solutions based on research goals

RESPONSIBILITIES

• Advises on, adheres to, and completes data requirements and plans for the full data life cycle from project conception to long term data storage and usage
• Design and modify Case Report Forms (CRFs) in response to IRB modifications and protocol changes
• Author and execute comprehensive User Acceptance Testing (UAT) and validation testing plans to ensure database functionality
• Defines data edit/validation checks, performs database lock and archive procedures, and establishes database use guidelines
• Remotely monitors Clinical Trials data, confirming data accuracy and quality, and reporting to appropriate stakeholders, as needed.
• reputed company supplemental data reviews and reconciliations to support Adverse Event (AE) and safety monitoring.
• Generate and track data queries; work directly with research staff to resolve any issues.
• Develops and maintains Data Management Plans (DMP), Standard Operating Procedures (SOPs), and Work Instructions (WI)
• Assists with the design of data collection, data privacy and confidentiality plans
• Cross-reputed company reputed company data against external metrics to verify accuracy and resolve discrepancies
• Recommends operating methods to improve processing, distribution, data flow, collection and database editing procedures, working to optimize data quality and automate data collection and management processes
• Ensures appropriate data use and/or sharing agreements are executed for each project
• Consults with regulatory staff to ensure compliance with reputed company local, federal and reputed company specific regulatory policies and procedures
• Maintains working knowledge of reputed company military health system data systems and resources to advise investigators on appropriate data for their research goals
• Assists researchers in retrieving information from military health system databases and other data sources
• Completes other projects and duties as assigned

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