Manager, Data Management Program Lead, Hematology

Scorpion Therapeutics; United States; On-site; USD 130,000 - 170,000; Full time

Job summary

Scorpion Therapeutics is seeking a Program Lead in Data Management to oversee multiple clinical studies from a data perspective, with a strong emphasis on oncology and data quality, timeliness, and regulatory compliance.

The role drives process improvements, ensures inspection readiness, and may serve as the primary data contact for day-to-day activities across studies and programs. Experience in leading study teams and CRO/vendor oversight is required.

Qualifications

• 8+ years of clinical data management experience in biopharma.
• At least 5 years in a lead role.
• Strong oncology background.
• Proficiency in EDC systems like Medidata Rave.
• Bachelor's degree or equivalent preferred.

Responsibilities

• Lead study teams.
• Manage vendor relationships (CROs, labs).
• Develop and review EDC databases.
• Perform data validation.
• Contribute to protocol and analysis document review.
• Support process standardization and inspection readiness.
• May act as the primary data contact and oversee day-to-day data management activities.

Skills

Project management

Cross-functional collaboration

Process development

ICH/regulatory knowledge

Microsoft Office

Data visualization

Education

Bachelor's degree

Tools

Medidata Rave

Job description

Role: Program Lead in Data Management overseeing multiple clinical studies or programs, primarily in oncology, from a data perspective. Objectives include ensuring data quality, timeliness, compliance, and process improvement within clinical data management.

Responsibilities

• lead study teams
• manage vendor relationships (CROs, labs)
• develop and review EDC databases
• perform data validation
• contribute to protocol and analysis document review
• support process standardization and inspection readiness.
• May act as the primary data contact and oversee day-to-day data management activities.

Requirements

• 8+ years of clinical data management experience in biopharma
• at least 5 years in a lead role
• strong oncology background
• proficiency in EDC systems like Medidata Rave
• Bachelor's degree or equivalent preferred.

Skills

• project management
• cross-functional collaboration
• process development
• knowledge of ICH/regulatory standards
• proficiency in Microsoft Office and visualization tools.

Travel may be required for domestic and international sites.

High-value: oncology, clinical trials, data management leadership, EDC systems, regulatory compliance, and process improvement.

Work setup: not specified.