eCOA - Clinical Study Build Programmer

Scorpion Therapeutics; Indiana (PA); On-site; USD 90,000 - 130,000; Full time

Job summary

Scorpion Therapeutics in the United States is seeking a Clinical Study Build Programmer - eCOA to design, program, test, and implement clinical data collection databases for global trials.

The role involves configuring eCOA/EDC platforms, developing study forms, and ensuring data standards, while supporting regulatory submissions and collaborating with Data & Analytics to deliver accurate data systems.

Qualifications

• Master's degree in a relevant field.
• 3+ years in clinical data management or related analytics.
• Proficiency in data systems, data standards and programming.

Responsibilities

• Configure eCOA/EDC platforms and develop study forms.
• Ensure data standards and data quality across trials.
• Support data submission and regulatory activities.
• Collaborate with Data & Analytics teams to deliver robust data systems aligned with study objectives.
• Report progress with focus on risk management in a GxP environment.

Skills

Clinical data systems

Data standards

Programming

eCOA data flow

Clinical development knowledge

Data tools familiarity

International travel readiness

Education

Master's degree in Informatics, Life Sciences, or related

Job description

Role

Clinical Study Build Programmer - eCOA, responsible for designing, programming, testing, and implementing clinical data collection databases for global trials.

Core responsibilities

Configuring eCOA/EDC platforms, developing study forms, ensuring data standards, supporting data submission and regulatory activities, and collaborating with Data & Analytics teams to deliver accurate, efficient data systems aligned with study objectives.

Requirements

• Master's in Informatics, Life Sciences, or related
• 3+ years in clinical data management or equivalent experience in data analytics, statistics, or IT
• Proficiency in clinical data systems, data standards, and programming

Preferred

• Experience with eCOA data flow
• Clinical development knowledge
• Familiarity with data tools
• International travel readiness

High-value specifics

• Supportive of multiple therapeutic areas
• Clinical trial phases (preclinical to Phase 3)
• Regulatory compliance (ICH, GCP, FDA)
• Technical platforms involved in global data collection efforts

Reporting

Reporting to project leaders, with a focus on process improvement and risk management in a GxP environment.

Work Setup

Not specified but implies collaboration across global teams and potential international travel.