Clinical Data Manager – Level 2

ASRC Federal

. Manage the delivery of high-quality data from project start-up and planning through project execution and project closeout across several projects .

Posted 9/19/2026full-timeRemote • Texas • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trial data, ensuring compliance with federal regulations and Good Clinical Practices. Proficient in data management processes, quality control, and the development of clinical data reports.

Highest-signal resume keywords

Clinical Data ManagementQuality ControlGood Clinical PracticeData AbstractionDatabase Design

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data EntryData ValidationData ReportingClinical Trial ManagementQuality AssuranceData ProcessingProtocol ComplianceClinical Data ReviewData TrackingDatabase Testing

Soft Skills

Client CommunicationProject Management

Tools & Technologies

Clinical DatabasesReporting Tools

Industry Keywords

Clinical ResearchFederal RegulationsGood Clinical Data Management PracticesStandard Operating ProceduresPatient Protocol

About the role

Key responsibilities & impact

Manage the delivery of high-quality data from project start-up and planning through project execution and project closeout across several projects
Independently perform project-specific quality control and quality assurance tasks
Ensure consistency, accuracy, and adherence to federal regulations, Good Clinical Practice, Good Clinical Data Management Practices, SOPs, and Working Instructions
Manage patient protocol information and incorporate protocol-specific guidelines into clinical trial data review
Contribute to the design of databases and forms for clinical data entry and reporting
Test new clinical trial data-management processes and systems
Test clinical trial databases and data-entry screens for protocol and institutional compliance
Process, track, and validate data accurately and on time
Perform data abstraction and data entry across multiple clinical research databases and protocols
Develop and extract patient clinical data reports for publications and presentations
Use clinical databases and reporting tools
Identify project-specific reports and assist in their development
Prepare, review, and submit clinical data to monitoring agencies
Maintain client communication on data-management project status and review key project questions

Requirements

What you’ll need

A bachelor's degree
2 years of experience in a related or applicable field, or an equivalent combination of education and experience
Experience in Medical, Clinical or Research environment