Senior Clinical Data Manager — EDC & Trials

Intuitive; California (MO); On-site; USD 90,000 - 120,000; Full time

Job summary

Intuitive is seeking a Clinical Data Management professional to lead design, validation, and maintenance of clinical databases tied to pre- and post-market studies. You will collaborate with clinical operations to ensure high-quality data management and regulatory compliance.

The role requires 3–5 years in data management within the medical devices field, experience with EDC systems such as Medrio and Medidata Rave, and strong knowledge of GCP and clinical research processes.

Qualifications

• Minimum 3–5 years of data management experience in medical devices/pharma.
• Experience with EDC systems (Medrio, Medidata Rave) is preferred.
• Knowledge of Good Clinical Practices and regulatory terminology.

Responsibilities

• Design and manage data collection, validation, and lifecycle documentation.
• Interpret protocol requirements for efficient EDC design.
• Create design specs for clinical databases and edit checks.
• Validate EDCs at study level; develop requirements, test scripts, and UAT.
• Administer EDC systems across multiple studies; train users on systems.
• Support data listings generation and data transfers for stats review.

Skills

Data management

GCP knowledge

Clinical research basics

Education

BSc/BA in scientific/medical field

Tools

Medrio

Medidata Rave

SAS

Job description

Intuitive is seeking a Clinical Data Management professional to lead design, validation, and maintenance of clinical databases tied to pre- and post-market studies. You will collaborate with clinical operations to ensure high-quality data management and regulatory compliance.

The role requires 3–5 years in data management within the medical devices field, experience with EDC systems such as Medrio and Medidata Rave, and strong knowledge of GCP and clinical research processes.