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Data Coordinator
Premier Research. Prepare documentation, including CCGs, Data Management Plans, Data Report Specifications, and External Data Transfer Specifications .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Clinical Data Management, including documentation preparation, user acceptance testing, and database maintenance. Proficient in generating reports and ensuring compliance with protocols while supporting project management and quality control activities.
Highest-signal resume keywords
Clinical Data Management System (CDMS)User Acceptance TestingData EntryDocumentation ComplianceAnalytical Problem-Solving
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 Management PlansData Report SpecificationsExternal Data Transfer SpecificationsDatabase MaintenanceQuery GenerationCRF ReviewData ReconciliationQuality Control (QC)Report GenerationTest Data Development
Soft Skills
Analytical SkillsInvestigative SkillsOrganizational SkillsCustomer-Service MindsetMultitasking Ability
Tools & Technologies
Medidata RaveCalyx EDC
Industry Keywords
Clinical ResearchTrial Master File (TMF)Data ReviewStudy MetricsFast-Paced Environment
About the role
Key responsibilities & impact- Prepare documentation, including CCGs, Data Management Plans, Data Report Specifications, and External Data Transfer Specifications
- Assist with developing standard test data and provide feedback on testing results
- Perform user acceptance testing on studies, including edit-check testing
- Maintain databases and support database updates
- Perform data entry
- Generate reports for data review
- Review CRFs, data listings, and databases for protocol and documentation compliance
- Generate queries to internal or external personnel to resolve problematic data
- Review query responses and resolve discrepancies
- Perform external data and serious adverse event reconciliation
- Act as Lead Data Coordinator and/or Safety Reviewer on multiple studies
- Submit documents to the Trial Master File (TMF)
- Support TMF Quality Control activities
- Perform database QC activities
- Perform QC of study reports and CRF archive files
- Support Data Scientists and/or Project Managers with financial project statistics, study metrics, dashboard updates, and project status reporting
Requirements
What you’ll need- Bachelor’s Degree or above (preferably in a Life Science)
- 2–4 years of DM mastery or related clinical research industry experience
- Knowledge of at least one Clinical Data Management System (CDMS), e.g. Medidata Rave or Calyx EDC
- Fluent in English (written and spoken)
- Strong analytical, investigative, and problem-solving skills
- Proven ability to learn, navigate, and leverage new systems quickly
- Exceptional organizational skills and high attention to detail
- Customer-service mindset
- Ability to multitask and balance competing priorities in a fast-paced environment
Benefits
Comp & perks- Flexibility and balance to support employees’ lives
- Skills and opportunities for professional growth and development