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Job Details

Clinical Data Manager

  2026-02-04     The Geneva Foundation     all cities,AK  
Description:

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 (EDC) 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 Department of Defense regulatory requirements. Working cross-functionally with investigators, research staff, statisticians, and regulatory teams, the Clinical Data Manager ensures data integrity, 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 (EDC) 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 Excel and other Microsoft Software
  • Excel Macros experience a plus
  • Demonstrated competence in oral and written communication
  • Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
  • Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
MANAGEMENT RESPONSIBILITIES
  • Oversees quality assurance of all study databases, proactively tests data to identify data integrity 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.
  • Perform 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-check EDC 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 all local, federal and Department of Defense specific regulatory policies and procedures
  • Maintains working knowledge of all 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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