Clinical Data Manager, Senior

Delfi Diagnostics

. Perform ongoing data cleaning and query management in the study EDC and data collection systems .

Posted 9/18/2026contractRemote • United StatesSenior💰 $70 - $85 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical data management, including database lock activities and statistical analysis plan interpretation. Proficient in data cleaning, query management, and documentation of derived variable specifications.

Highest-signal resume keywords

Clinical Data Management ExperienceMedidata Rave EDC ProficiencyDatabase Lock Activities SupportStatistical Analysis Plan InterpretationR Programming Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data CleaningQuery ManagementMedical Coding SupportData ReconciliationDerived Variable SpecificationsStatistical ProgrammingTFL Specifications

Soft Skills

Organizational SkillsWritten CommunicationVerbal Communication

Tools & Technologies

DELFIClarioAI Tools

Industry Keywords

PharmaceuticalMedical DeviceCROOncologyIVD Studies

About the role

Key responsibilities & impact

Perform ongoing data cleaning and query management in the study EDC and data collection systems
Conduct data review, discrepancy management, medical coding support as needed, and reconciliation activities, including sample-to-clinical data reconciliation
Work from data quality report output produced by DELFI's data team, translating findings into queries and resolutions
Support CRF freeze/lock readiness and database lock preparation
Participate in study team meetings and provide brief weekly written status summaries covering work completed and risks/blockers
Develop and finalize Derived Variable specifications and requirements documentation using DELFI templates and conventions
Support Table, Figure, and Listing specifications, including review against the Statistical Analysis Plan
Provide limited statistical programming or implementation support for derived variables and TFL-related datasets, as skills allow

Requirements

What you’ll need

3–5+ years of hands-on clinical data management experience in a pharmaceutical, medical device/diagnostic company, or CRO
Direct experience supporting database lock activities in clinical trials
Proficiency with Medidata Rave EDC
Ability to work independently with minimal ramp-up
Excellent organizational, written, and verbal communication skills
Senior level: 5+ years of CDM experience, including experience authoring DV and/or TFL specifications
Senior level: Ability to read and interpret a Statistical Analysis Plan and translate it into specification documents
Preferred: Experience in oncology, diagnostics, or IVD/regulated device studies
Preferred: R programming experience
Preferred: Familiarity with leveraging AI tools such as Claude Code or Gemini to streamline clinical data management workflows, data review, or scripting tasks
Preferred: Familiarity with Clario or comparable imaging/adjudication data platforms