Senior Manager, Data Management Program Lead, Hematology

Scorpion Therapeutics

United States

On-site

USD 180,000 - 250,000

Full time

14 days+
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Job summary

Scorpion Therapeutics in the United States is seeking a Program Lead in Data Management to oversee multiple clinical studies and programs in oncology, ensuring data quality, regulatory compliance, and process efficiency.

You will lead data management activities, oversee the data team, and collaborate with cross-functional teams and CROs/labs, developing and reviewing data-related documentation while driving process improvements and audit readiness. Travel may be required.

Qualifications

  • Minimum 8+ years in clinical data management within biotech/pharma.
  • Strong oncology experience.
  • 5+ years as a Lead Data Manager.
  • Proficiency in EDC systems (Medidata Rave preferred).
  • General knowledge of ICH/regulatory standards.

Responsibilities

  • lead data management activities
  • oversee data team performance
  • collaborate with cross-functional teams
  • liaise with vendors (CROs, labs)
  • develop and review data-related documentation
  • support process improvements
  • ensure audit readiness

Job description

Role:

Program Lead in Data Management overseeing multiple clinical studies and programs in oncology, ensuring data quality, compliance, and process efficiency.

Responsibilities:
  • lead data management activities
  • oversee data team performance
  • collaborate with cross-functional teams
  • liaise with vendors (CROs, labs)
  • develop and review data-related documentation
  • support process improvements
  • ensure audit readiness
Requirements:
  • minimum 8+ years in clinical data management within biotech/pharma
  • strong oncology experience
  • 5+ years as a Lead Data Manager
  • proficiency in EDC systems (Medidata Rave preferred)
  • general knowledge of ICH/regulatory standards.
Preferred:
  • experience developing data standards
  • influencing cross-functional teams
  • working in GxP environments.
HighValue:
  • oncology
  • biologics or small molecules
  • clinical phase (implied post-IND with ongoing studies)
  • cross-functional leadership
  • vendor oversight
  • process development.
WorkSetup:

travel may be required (domestic/international); individual contributor role.

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