Senior Remote Clinical Data & EDC Programmer

ICON San Antonio; Bogotá; À distance; COP 453 148 000 - 614 986 000; Plein temps

Avantages offerts par ce poste

Competitive salary

Flexible work arrangements

Health insurance

Retirement planning

Résumé du poste

ICON is seeking a Principal Clinical Data & EDC Programmer to join our global team. Remote or Hybrid work arrangements across the Americas and beyond enable you to lead programming for CDMS, non-CDMS components, and analytics solutions in clinical trials.

You will mentor colleagues, collaborate with data managers and biostatisticians, and drive improvements in data management processes using SAS, R, Python, and SQL in a fast-paced environment.

Qualifications

• 10+ years of experience in EDC programming (Medidata Rave and/or Veeva) in clinical trials.
• Proficiency with SQL and SAS programming for vendor data imports or DM reconciliation.
• Experience leading studies, training, and mentoring junior programmers.
• Strong problem-solving and communication skills for cross-functional teams.
• Experience with R and Python preferred; bachelor’s degree in a relevant field.

Responsabilités

• Develop, validate, and maintain programming solutions for CDMS (Rave/Veeva), data validation outputs and custom reports.
• Create programs for external vendor data handling using SAS/R/SQL and data extraction.
• Collaborate with data managers, project managers, and biostatisticians to integrate programming solutions.
• Serve as main contact during study setup and maintenance for system programming questions.
• Provide mentorship and training to other programmers and share knowledge across the team.
• Lead innovative analytics techniques, automation strategies, and process improvements.

Connaissances

EDC programming

Project leadership

Communication

Problem solving

Mentoring

Attention to detail

Formation

Bachelor’s degree in a relevant field

Outils

Medidata Rave

Veeva

SQL

SAS

R

Python

Description du poste

ICON is seeking a Principal Clinical Data & EDC Programmer to join our global team. Remote or Hybrid work arrangements across the Americas and beyond enable you to lead programming for CDMS, non-CDMS components, and analytics solutions in clinical trials.

You will mentor colleagues, collaborate with data managers and biostatisticians, and drive improvements in data management processes using SAS, R, Python, and SQL in a fast-paced environment.