Director, Clinical Data Management, Digital Health Technologies, Hybrid

Scorpion Therapeutics; Pennsylvania; Hybrid; USD 180,000 - 240,000; Full time

Job summary

Scorpion Therapeutics seeks a senior leader to oversee global clinical data management, emphasizing strategic planning, vendor governance, quality oversight, and team development across a complex research portfolio.

Responsibilities include directing data management activities across trials, establishing objectives aligned with corporate goals, managing vendor relationships and KPIs, and driving SOP development and innovative processes in a hybrid US-based role, with ~10% travel.

Qualifications

• Bachelor's degree in a health or science-related field.
• 12+ years in clinical data management or operations.
• 5+ years in management; extensive experience with digital health technologies, COA, and IRT; strong knowledge of drug development processes, GxP, GCP, and regulatory standards.

Responsibilities

• Direct data management activities across clinical research.
• Develop high-level objectives aligned with organizational goals.
• Manage vendor relationships and KPIs.
• Oversee SOP development.
• Lead process or technological innovations.

Skills

Leadership

Strategic planning

Vendor governance

Team development

Education

Bachelor's degree in health/science

Tools

COA

IRT

Job description

Role:

Senior leader overseeing global clinical data management functions, with a focus on strategic planning, vendor governance, quality oversight, and team development within a complex research portfolio.

Responsibilities:

direct data management activities across clinical research, develop high-level objectives aligned with organizational goals, manage vendor relationships and KPIs, oversee SOP development, and lead process or technological innovations.

Qualifications:

Bachelor's degree in a health or science-related field; 12+ years in clinical data management or operations; 5+ years in management; extensive experience with digital health technologies, COA, and IRT; strong knowledge of drug development processes, GxP, GCP, and regulatory standards.

High-Value:

global scope, leadership in data management supporting clinical trials across multiple therapeutic areas, with a focus on innovation, vendor management, and compliance.

Work Setup:

hybrid in a US-based location, with approximately 10% travel.