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Clinical Data Associate II
Worldwide Clinical Trials. Perform data cleaning activities, including query review and closure, to support data quality and study timelines .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical data management, including data cleaning, quality assessment, and user acceptance testing of EDC databases. Proficient in preparing study-specific metrics and managing documentation for clinical trials.
Highest-signal resume keywords
Clinical Data CleaningUser Acceptance Testing (UAT)Database Quality Assessment (DQA)SAS Listings ReviewData Management Metrics Preparation
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Data CleaningQuery ReviewDatabase ReviewData ReconciliationClinical Trial DocumentationFinal Study Document SubmissionData Quality AssessmentEDC Database TestingSAS Data ChecksTrial Master File Management
Soft Skills
Attention to DetailCommunicationCollaboration
Industry Keywords
Clinical ResearchBiomedical SciencesLife SciencesData ManagementClinical Trials
About the role
Key responsibilities & impact- Perform data cleaning activities, including query review and closure, to support data quality and study timelines
- Review database pages and identify data issues to ensure accurate and complete clinical trial records
- Prepare and distribute study-specific data management metrics to internal and external stakeholders
- Conduct User Acceptance Testing (UAT) of EDC databases
- Review third-party vendor data reconciliations and help resolve discrepancies
- Perform Database Quality Assessment (DQA) reviews
- Review SAS listings and data checks, taking appropriate action on queries and findings
- Prepare end-of-study media and documentation for trial archival activities
- Submit final study documents to the Trial Master File
Requirements
What you’ll need- Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, a related discipline, or equivalent relevant experience
- Minimum of 1 year of relevant industry experience in clinical research, data management, or a related field
- Proficiency in English
- Experience with clinical data cleaning, query review and closure
- Experience reviewing database pages and identifying data issues
- Experience preparing study-specific data management metrics
- Experience conducting User Acceptance Testing (UAT) of EDC databases
- Experience with third-party vendor data reconciliations
- Experience performing Database Quality Assessment (DQA) reviews
- Experience reviewing SAS listings and data checks
- Experience preparing end-of-study media and documentation
- Experience submitting final study documents to the Trial Master File
Benefits
Comp & perks- Equal employment opportunities
- Diverse and inclusive work environment
- Collaboration and creativity-focused workplace
- Supportive and cohesive teams
- Accessible leadership
- Opportunity to work with global teams across multiple time zones