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Shoulder Innovations

Clinical Data Associate

Shoulder Innovations

Clinical Data Associate managing data across study lifecycle for a medical device startup. Responsibilities include data management, EDC usage, and Power BI reporting.

Posted 7/19/2026full-timeRemote • Missouri • 🇺🇸 United StatesJuniorMid-Level💰 $70,000 - $85,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Proficient in data management tasks including data review, query generation, and reconciliation across various data streams. Experienced in utilizing EDC systems and Power BI for reporting and tracking data quality metrics in clinical research settings.

Highest-signal resume keywords
EDC System ProficiencyPower BI Dashboard ManagementClinical Data Management ExperienceKnowledge of GCP and ICH StandardsStrong Excel Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Data ManagementQuery GenerationData ReconciliationReport GenerationData CleaningECRF ManagementData Quality MetricsProtocol Deviations TrackingDiscrepancy ReviewValidation Listings
Soft Skills
Cross-Functional CollaborationCommunication Skills
Tools & Technologies
Castor EDCRavePower BIMicrosoft ExcelMicrosoft Word
Industry Keywords
Clinical ResearchCROPharmaMedical DeviceBiotechGCPICHCDISCCDASH

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Perform comprehensive data management tasks including data review, query generation, and query resolution
  • Support all study phases: Start-up, Execution, Database Lock, and Close-out
  • Perform ongoing data reconciliation across all data streams (e.g., EDC, imaging, third-party vendors)
  • Review discrepancy/edit check output and validation listings per the Data Management Plan (DMP)
  • Resolve answered queries and re-query where appropriate
  • Manage eCRF freeze/lock activities
  • Support study closeout and archiving activities, including QC of subject/site CRFs
  • Serve as a proficient day-to-day user of the EDC system (e.g., Castor EDC, Rave, or equivalent)
  • Generate reports directly from the EDC system to track data cleaning progress and outstanding queries
  • Maintain Power BI dashboards and reports to track data cleaning status, query aging, site-level data quality metrics, and monitoring visit findings
  • Translate data management metrics (e.g., missing data, outstanding queries, protocol deviations) into clear visual reports for internal stakeholders

Requirements

What you’ll need
  • Bachelor's degree in a health, science, or related discipline, or equivalent experience in clinical research
  • Clinical data associate/management experience at a CRO, pharma, medical device, or biotech company
  • Hands-on experience with EDC systems required (Castor EDC, Rave, Inform, or equivalent)
  • Demonstrated proficiency managing reports/dashboards in Power BI (Power Query/M language experience a plus)
  • Knowledge of current industry standards (e.g., GCP, ICH, CDISC/CDASH)
  • Proficiency with Microsoft Office (Excel, Word); strong Excel skills required
  • Experience working in cross-functional, multi-site clinical trial teams

Benefits

Comp & perks
  • Great company culture
  • Opportunities for professional growth
  • Competitive wages
  • Benefits