Associate Director - Study Integration Manager, Data Integration and Automation - Hybrid

Scorpion Therapeutics; Pennsylvania; Hybrid; USD 150,000 - 190,000; Full time

Benefits offered by this job

Hybrid work model

Travel opportunities

Job summary

Scorpion Therapeutics seeks a Lead Study Integration for clinical data management to ensure quality and regulatory compliance across eCRFs, data integrations, and reporting. You will develop program plans, coordinate cross-functional activities, and drive risk mitigation and change control while overseeing validation and audit readiness.

The role requires a Bachelor's with 8+ years in clinical data management (including 2 years of people leadership) or an advanced degree with 4+ years of

Qualifications

• Bachelor's degree with 8+ years in clinical data management or related fields, including 2 years of people management.
• Advanced degree with 4+ years of relevant experience, including 2 years of leadership.

Responsibilities

• Lead study integration for clinical data management, ensuring quality and compliance across eCRFs, integrations, and reports.
• Develop program plans and manage cross-functional coordination.
• Mitigate risk, manage change control, and oversee validation and audit readiness.
• Direct leadership of complex trials, drive process improvement initiatives, and mentor the team.

Skills

Clinical data management

People leadership

GxP experience

Audit readiness

Stakeholder engagement

Education

Bachelor's degree

Advanced degree

Tools

Automation tools

Job description

Role

Lead study integration for clinical data management, ensuring quality and compliance in trial data components such as eCRFs, integrations, and reports. Responsibilities include developing program plans, managing cross-functional coordination, risk mitigation, change control, and overseeing validation and audit readiness. The role involves direct leadership of complex trials, process improvement initiatives, and team development.

Requirements

Bachelor's degree with 8+ years in clinical data management or related fields, including 2 years of people management; or an advanced degree with 4+ years of relevant experience, including 2 years of leadership.

High-Value

Experience with clinical trial lifecycle, GxP standards, validation, audit preparation, and data systems integrations; familiarity with automation tools and programming interfaces; strong stakeholder engagement skills.

Collaboration

Collaboration involves Clinical, DI&A/IT, service providers, and other stakeholders.

Work setup

hybrid with 10% travel.