Clinical Data Manager

Emerald Clinical

. Ensure completeness, quality, and integrity of clinical data in the database .

Posted 9/30/2026full-timeTaipei • TaiwanMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical data management, including data integrity, quality control, and project management. Proficient in developing data management documents and mentoring teams while managing budgets and timelines for clinical studies.

Highest-signal resume keywords

Data Management ExperiencePhase III Study LeadershipOncology Project ExperienceData Cleaning and Query ManagementECRF Specification Development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data ManagementData Validation PlansData Management PlansECRF Completion GuidelinesSAE ReconciliationDatabase UATQuality ControlData CleaningQuery ManagementStudy Metrics Tracking

Soft Skills

MentoringTrainingCommunication

Tools & Technologies

PDMS

Industry Keywords

MedicalPharmacyBiologyBiomedicalOncologyNephrologyMRCT TrialsClinical StudiesData Management DocumentationProject Budgets

About the role

Key responsibilities & impact

Ensure completeness, quality, and integrity of clinical data in the database
Perform, oversee, and be responsible for development of data management documents
Conduct database UAT and quality control
Perform data cleaning and query management activities
Act as a subject matter expert for one or more specific Data Management tasks
Assist in developing and implementing new technologies and department tools
Mentor and train Data Managers
Provide new project recommendations, attend bid defense meetings, and prepare for project interviews
Author and maintain eCRF specifications and Data Validation Plans
Develop and maintain Data Management Plans, eCRF completion guidelines, and SAE reconciliation plans
Manage local lab workflows, SAE reconciliation, and external data reconciliation
Track and report study metrics
Establish study timelines for data snapshots, database freeze/lock, and quality deliverables
Attend data review meetings when applicable
Archive Data Management documentation
Manage study timelines and estimate resource requirements
Manage project budgets, scope, work completed, and revenue forecasts
Update PDMS and handle project finance-related issues

Requirements

What you’ll need

Bachelor’s degree in medical, Pharmacy, Biology, Biomedical or related fields
6+ years of industry and Data Management experience
Experience independently leading Phase III studies as a lead data manager
Experience in oncology or nephrology projects
MRCT trial experience is preferred

Benefits

Comp & perks

Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience
Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role
Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role
Employee Wellbeing: Programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events
Global Opportunities: Exposure to diverse projects and clients through the company's international reach
Purpose-driven work contributing to clinical trials focused on therapies in renal, cardiometabolic, and oncology
Collaboration and innovation in a culture valuing diverse perspectives and creative solutions