Principal Clinical Programmer — Surgical Innovations

Edwards Lifesciences Gruppe; Redhill; Hybrid; GBP 100,000 - 141,000; Full time

Benefits offered by this job

Hybrid work model

Performance-based incentives

Benefits programs

Job summary

Edwards Lifesciences is seeking a seniorClinical Programmer within Clinical Affairs to lead data management and programming for clinical trials. You will collaborate with investigators and regulatory bodies to optimize trial outcomes and drive high-quality evidence generation.

The role emphasizes Medidata programming, EDC expertise, and cross-functional leadership in a hybrid work setting, with strong emphasis on regulatory compliance and process improvement.

Qualifications

• Bachelor's Degree and at least 6 years in clinical research, data management, software programming or equivalent.
• Extensive experience with EDC systems; Medidata programming experience is required.

Responsibilities

• Provide technical expertise in clinical programming and lead data validation for trials.
• Lead cross-functional teams in design and delivery of complex modules and CRFs.
• Develop specifications for systems, upgrades, and IT integration with stakeholders.
• Create and deliver high-level training to end-users and junior staff.
• Identify resources for database implementation and evaluate external vendors.
• Oversee daily activities of outsourced systems for clinical trials.
• Contribute to SOPs, workflows, forms, and regulatory-compliant processes.

Skills

Clinical research

Data management

Medidata programming

EDC systems

C#

SQL

Education

Bachelor's degree

Tools

Medidata

Excel

Job description

Edwards Lifesciences is seeking a seniorClinical Programmer within Clinical Affairs to lead data management and programming for clinical trials. You will collaborate with investigators and regulatory bodies to optimize trial outcomes and drive high-quality evidence generation.

The role emphasizes Medidata programming, EDC expertise, and cross-functional leadership in a hybrid work setting, with strong emphasis on regulatory compliance and process improvement.