The Role

Veeva RTSM is changing the way clinical trial is managed in the industry. RTSM supports randomization and drug supply management with better product and services. The days of complex implementation and study conduct are gone; now research teams can make faster and more informed decisions.

What You’ll Do

Review protocols and include required modules in the User Requirements Specification (URS)

Perform highly skilled duties such as creating, reviewing, coordinating, and managing a variety of deliverables (including, but not limited to, timelines, KOM, URS, Communication Manual, Requirements for Subject Randomizations, and Clinical Trial Material Lists for assigned projects, User Acceptance Testing, and system set up)

Ensure established timelines are met

Facilitate and troubleshoot any issues associated with managing the delivery of RTMS systems

Provide technical advice and assistance to other project...