Clinical Data Manager

Worldwide Clinical Trials

. Lead and oversee clinical data management activities across multiple complex global studies from start-up through closeout .

Posted 10/9/2026full-timeRemote • ArgentinaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical data management, including leading global studies, developing trial documentation, and ensuring data integrity. Proficient in coordinating resources, managing vendor activities, and driving continuous improvement initiatives.

Highest-signal resume keywords

Clinical Data ManagementData Management PlansUser Acceptance TestingData CleaningVendor Data Reconciliation

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data ManagementData Management PlansDatabase SpecificationsEdit Check SpecificationsData CleaningUser Acceptance TestingRisk MonitoringProcess ImprovementMetrics AnalysisTrial Documentation

Soft Skills

LeadershipCommunicationCollaborationProblem-SolvingStakeholder Engagement

Industry Keywords

Biomedical SciencesLife SciencesPharmaceutical IndustryBiotechnologyMedical Device IndustryClinical TrialsData Management Best Practices

About the role

Key responsibilities & impact

Lead and oversee clinical data management activities across multiple complex global studies from start-up through closeout
Coordinate resources to ensure data management deliverables are completed on time and within budget
Develop and maintain trial documentation, including data management plans, database specifications, edit check specifications, and related study materials
Drive effective user acceptance testing (UAT) for database builds and study execution
Manage vendor data reconciliation activities and define specifications for reconciliation outputs
Oversee data cleaning to ensure accurate, complete, and reliable clinical trial data
Monitor study progress through key metrics, identify risks, and communicate concerns to data management leadership
Partner with internal and external stakeholders in study meetings and cross-functional discussions
Lead or contribute to process reviews and continuous improvement initiatives

Requirements

What you’ll need

Bachelor's degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experience
Minimum 3 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries
Working knowledge of clinical data management best practices and technologies used in clinical trials

Benefits

Comp & perks

Diverse and inclusive work environment
Collaborative and supportive teams
Accessible leadership
Equal employment opportunities
Employee experiences where everyone is respected and has access to equal opportunity