Clinical Data Associate

Shoulder Innovations

. Perform comprehensive data management tasks including data review, query generation, and query resolution .

Posted 10/12/2026full-timeRemote • Michigan • United StatesJuniorMid-Level💰 $70,000 - $85,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Proficient in clinical data management with expertise in EDC systems, data reconciliation, and report generation. Strong analytical skills in managing data quality metrics and translating data into visual reports for stakeholders.

Highest-signal resume keywords

Clinical Data ManagementEDC System ProficiencyPower BI Dashboard ManagementData ReconciliationGCP Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data ReviewQuery GenerationData CleaningData Quality ChecksReport GenerationExcel ProficiencyPower QueryDatabase Lock ManagementDocumentation FilingClinical Trial Support

Soft Skills

Cross-Functional CollaborationCommunicationProblem-Solving

Tools & Technologies

Castor EDCRaveInformPower BIMicrosoft Office

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, including EDC, imaging, and third-party vendors
Review discrepancy/edit check output and validation listings per the Data Management Plan
Resolve answered queries and re-query where appropriate
Receive and reconcile imaging data
Manage eCRF freeze/lock activities
File documentation in the Trial Master File
Support study closeout and archiving activities, including QC of subject/site CRFs
Serve as a proficient day-to-day user of the EDC system, including form/field configuration awareness, user access, and data export
Generate EDC reports to track data cleaning progress and outstanding queries
Perform DM quality review and internal QC checks
Support EDC-related testing during study build and amendments
Maintain Power BI dashboards and reports tracking data cleaning status, query aging, site-level data quality metrics, and monitoring visit findings
Translate data management metrics into clear visual reports for internal stakeholders
Maintain and troubleshoot Power Query/Power BI data pipelines
Ensure dashboard data accuracy through reconciliation against EDC source data
Attend study-related meetings and teleconferences
Track project progress and issue periodic status/metric reports
Assist in identifying achievement of milestones per study timelines
Participate in finalization and transfer of the clinical database and related documents to the sponsor
Participate in internal meetings and internal/external audits as required
Maintain awareness of contract scope and study-specific Clinical Data Management Plans

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 is 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