Director, Global eCOA Management – Hybrid/Remote

Bristol Myers Squibb

Madison (WI)

Hybrid

USD 201,000 - 244,000

Full time

14 days+
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Benefits offered by this job

Health Coverage
Wellbeing programs
401(k)
Paid Time Off

Job summary

Bristol Myers Squibb is seeking a Director, eCOA Management to lead the operationalization of eCOA for clinical trials, reporting to the Head of Clinical Data Acquisition in GDM. This full-time, office-based role offers up to 50% remote work and is based in New Jersey with global responsibilities.

Responsibilities include leadership of the eCOA function, vendor management, ensuring data quality and readiness for analysis, and driving continuous improvement across studies and therapeutic areas.

Qualifications

  • Bachelor’s degree required with an advanced degree preferred.
  • At least 10 years of eCOA, end-to-end processes, and technology experience in neuroscience rater studies.
  • Proven track record of leading functions, managing staff, influencing stakeholders and vendors.

Responsibilities

  • Provide comprehensive leadership of the eCOA Management function.
  • Ensure quality development and timely delivery of eCOA instruments and devices.
  • Ensure data quality and readiness for downstream analysis.
  • Define processes for acquisition and review of eCOA data across studies and vendors.
  • Streamline templates and communications across vendors.
  • Define KPIs and drive improvements.
  • Lead initiatives to establish industry-leading eCOA capabilities.
  • Resolve complex issues and develop cross-functional solutions.
  • Forecast resource needs and manage eCOA book of work.
  • Lead a global team and support staff development and retention.
  • Engage with external organizations related to eCOA.

Skills

eCOA operationalization
Vendor management
Global team leadership
GCP/ICH knowledge
SDLC and system validation
Strategic project delivery

Education

Bachelor’s degree
Advanced degree preferred

Tools

eCOA platforms
Clinical data systems

Job description

Bristol Myers Squibb is seeking a Director, eCOA Management to lead the operationalization of eCOA for clinical trials, reporting to the Head of Clinical Data Acquisition in GDM. This full-time, office-based role offers up to 50% remote work and is based in New Jersey with global responsibilities.

Responsibilities include leadership of the eCOA function, vendor management, ensuring data quality and readiness for analysis, and driving continuous improvement across studies and therapeutic areas.

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