Senior Director, Data Management

DBV Technologies

. Lead clinical data management at DBV Technologies, a biopharmaceutical company developing treatments for food allergy .

Posted 10/22/2026full-timeWarren • New Jersey • United StatesSenior💰 $200,000 - $280,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates mastery of global data management processes, including oversight of Electronic Data Capture (EDC) systems and adherence to regulatory requirements. Proficient in managing data quality and integrating pharmacovigilance data streams for comprehensive analysis.

Highest-signal resume keywords

Mastery Of Global Data Management ProcessesStrong Experience With Electronic Data Capture (EDC) SystemsAdvanced Knowledge Of CDISC SDTM And ADaM Data StandardsProficiency In SAS Programming LanguageExperience With ePRO Solutions

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data Management ProcessesElectronic Data Capture (EDC)CDISC SDTMADaM Data StandardsSAS ProgrammingData Quality ManagementData Pipeline DevelopmentDatabase Lifecycle ManagementStatistical AnalysisData Integration

Soft Skills

LeadershipCollaborationCommunicationOversightDelegation

Tools & Technologies

Medidata RaveJMPJMP LiveRPython

Industry Keywords

BiopharmaceuticalClinical Data ManagementPharmacovigilanceSignal DetectionRegulatory Compliance

Tech Stack

Tools & technologies

Python

About the role

Key responsibilities & impact

Lead clinical data management at DBV Technologies, a biopharmaceutical company developing treatments for food allergy
Move core data collection and standards work, including EDC build and SDTM configuration, from external vendors to an internal team
Maintain data quality and regulatory requirements
Work with Clinical, Biostatistics, Safety, and Regulatory colleagues
Direct the data management work of CRO partners
Build out the internal data management team
Provide senior oversight of data management processes from CRF development to SDTM programming
Standardize study monitoring reports and data management metrics directly from EDC
Support integration and management of pharmacovigilance data streams for signal detection, regulatory, and analytical needs
Oversee global CRO data management activities and delegate tasks to the internal team
Manage database lifecycle activities, including freeze, lock, and archiving
Support existing studies and develop data pipelines for prospective studies

Requirements

What you’ll need

Mastery of global Data Management processes
Strong experience with Electronic Data Capture (EDC) systems, particularly Medidata Rave
Experience with ePRO (electronic Patient Reported Outcomes) solutions
Advanced knowledge of CDISC SDTM and ADaM data standards
Proficiency in SAS programming language
Experience with JMP, JMP Live, R, Python, or other data science tools is highly desirable