Clinical Data Manager I

Everest Clinical Research

. Plan, manage, control, and perform data processing and management activities for assigned projects .

Posted 9/30/2026full-timeTaipei City • TaiwanJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial data management, including data processing, quality control, and regulatory compliance. Proficient in leading projects, training personnel, and ensuring adherence to industry standards and practices.

Highest-signal resume keywords

Clinical Trial Data ManagementProject Management SkillsDatabase Validation ChecksQuality Control ProcessesLeadership in Data Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data ProcessingData Management TechniquesCase Report Form DesignDatabase Schema ReviewData Capture ValidationQuery WritingStandard Query LibrariesData Coding Discrepancy ResolutionData Management DocumentationArchiving Clinical Trial Data

Soft Skills

LeadershipTraining and SupervisionCoordinationCommunication

Industry Keywords

Good Working PracticesSOPsPharmaceutical Clinical Trial RegulationsClinical Trial DataflowQuality Control

About the role

Key responsibilities & impact

Plan, manage, control, and perform data processing and management activities for assigned projects
Lead data processing and management projects using project management skills and data management techniques
Manage timelines and coordinate activities for assigned projects
Specify and maintain database validation checks for assigned studies and therapeutic/drug-area modules
Define and monitor clinical trial dataflow and quality control processes according to SOPs, Good Working Practices, and unit guidelines
Train clinical trial site monitors on dataflow and QC processes
Design and review patient Case Report Forms and database schemas
Test data capture and entry screens
Validate electronically captured data
Write queries for missing data and data failing range or logical checks
Build and maintain standard query libraries
Perform QC during trials and database closure checks at study completion
Train and supervise Data Entry personnel and junior data management personnel
Validate and distribute study progress status reports to internal and external study team members
Assist in resolving data coding discrepancies
Prepare data management documentation for final archival and assist with archiving clinical trial data and study documentation
Assist data management QA personnel with QA procedures on trial CRFs, database schemas, and databases

Requirements

What you’ll need

Bachelor's degree in health and/or pharmaceutical sciences, physical/biological sciences, or chemistry, plus at least 2 years of experience in clinical trial data capture and management; OR a Master's or Ph.D. degree in these fields plus at least 1 year of relevant experience
In-depth understanding of clinical trial data management concepts, processes, procedures, relevant issues, pharmaceutical clinical trial regulations, industry guidance, conventions, and standards
Strong leadership in clinical data management activities
Desire to excel in leading data management projects

Benefits

Comp & perks

Full-time employment
Remote location listing, although the role description specifies on-site work in the Taipei, Taiwan office
Equal opportunity employment
Accommodations available for candidates with disabilities upon request