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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Associate Director - External Data Acquisition and Delivery

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeWarren, NJ, USA$154.8k - $252.8k /yr

About the Job

Requirements

  • A minimum of 10 years of experience in clinical data acquisition or management within the biotechnology, pharmaceutical, or healthcare industries.
  • A minimum of 4 years of people-management experience.
  • Demonstrated experience overseeing external data reconciliation activities between EDC systems and vendor platforms.
  • Experience driving process improvements and vendor oversight in supervised environments.
  • A bachelor's degree in Science, Health, Mathematics, Computing, Information Systems, or a related field.
  • Strong expertise managing multiple clinical external data types, including biomarker, imaging, eCOA, ECG, PK, genomics, laboratory, and Digital Health Technology data.
  • Advanced knowledge of external data reconciliation processes and EDC platforms such as Medidata Rave, Veeva, or Oracle Inform.
  • Experience working with SAS, CSV, and XML data formats.
  • Strong understanding of industry regulations, including 21 CFR Part 11, ICH-GCP, and CDISC standards.
  • Proven experience handling external vendor relationships and driving accountability for quality deliverables.
  • Strong leadership, people-management, coaching, and mentoring capabilities.
  • Strategic thinking, creativity, problem-solving, and analytical skills.
  • Strong project-management and stakeholder-management capabilities.
  • Excellent verbal and written communication skills.
  • Ability to work effectively in a fast-paced, matrixed, and global environment.

Responsibilities

  • Lead external data acquisition, integration, quality oversight, and delivery strategy across the clinical trial portfolio.
  • Serve as a portfolio-level lead for external data quality and clinical-data operational strategy.
  • Review protocol requirements, vendor specifications, and operational data flows.
  • Lead development and maintenance of Data Transfer Specification (DTS) documents to ensure compliance with company standards and timelines.
  • Provide expert mentorship on external data services, including biomarker, eSource, eCOA, imaging, ECG, PK, genomics, and laboratory data.
  • Drive external vendor oversight, onboarding, qualification, governance, and ongoing performance monitoring.
  • Establish and handle vendor KPIs, SLAs, and quality metrics.
  • Govern reconciliation activities between EDC systems and vendor data platforms to ensure data integrity and consistency.
  • Monitor reconciliation metrics, discrepancy trends, and resolution timelines across studies.
  • Collaborate with Database Development, Biostatistics, Study Data Managers, and external vendors to resolve complex data discrepancies.
  • Lead process-improvement initiatives, automation opportunities, and implementation of innovative external data solutions.
  • Manage and develop a team of EDAD Managers, Specialists, and associates through coaching, mentoring, and performance management.
  • Support SOP development, inspection readiness, audit activities, and regulatory compliance.
  • Represent EDAD in leadership forums, governance committees, and technology discussions.

Desired Qualifications

  • An advanced degree.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

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