Senior Clinical Data & EDC Programmer - Remote

ICON; United States; Remote; USD 110,000 - 160,000; Full time

Benefits offered by this job

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes andWell

Career development opportunities

Structured training and career Path

Job summary

ICON is seeking a Senior Clinical Data & EDC Programmer for remote/hybrid work across Canada, Mexico, Colombia and the United States. You will design, develop, and validate CDMS components (eCRFs, edit checks) and data pipelines using SAS, R, and Python, collaborating with cross-functional teams to meet trial needs.

The role requires 5+ years in EDC programming (Medidata Rave/Veeva) and strong data validation and reporting skills.

Qualifications

• 5+ years of experience with EDC programming (Medidata Rave and/or Veeva) and data validation outputs.
• Proficiency with SQL and/or SAS programming for vendor data imports or DM reconciliation outputs.
• Experience programming with R and Python (preferred).
• Bachelor’s Degree in a relevant field.

Responsibilities

• Develop, validate, and maintain programming solutions for CDMS (Rave/Veeva) and data outputs.
• Develop and maintain programs for external vendor data using SAS, R, and/or SQL.
• Collaborate with data managers, project managers, and biostatisticians to integrate programming solutions.
• Act as primary contact during study setup for programming questions by the project team.
• Mentor junior programmers and share knowledge within the group.
• Support improvements to technical systems and processes within an SME role.

Skills

EDC programming

SQL

SAS

R

Python

Data validation

Data review

Communication

Education

Bachelor’s Degree

Tools

Medidata Rave

Veeva

Job description

ICON is seeking a Senior Clinical Data & EDC Programmer for remote/hybrid work across Canada, Mexico, Colombia and the United States. You will design, develop, and validate CDMS components (eCRFs, edit checks) and data pipelines using SAS, R, and Python, collaborating with cross-functional teams to meet trial needs.

The role requires 5+ years in EDC programming (Medidata Rave/Veeva) and strong data validation and reporting skills.