Job Description:

• Responsible for understanding the specific study requirements (software, devices, etc…) associated with a given protocol design. This includes functional and non-functional requirements.

• Ultimate responsibility for the delivery of the technology products within the technology suite for clinical studies.

• Full awareness of the clinical study pipeline, connecting with clinical study teams.

• Deliver the “Digital Trial App products” for the study. Accountable for all or any combination of:

• Defining the functional scope of the app (which eCOAs, what patient experience, UX, other features part of the product(s)) in collaboration with study team or other cross functional teams supporting the study.

• Developing the overall study configuration and executing the overall study design within the Digital Trials platform suite.

• As needed: attend and provide training of the Digital Trials Platform product at Investigator meetings.

• Accountable for the overall packaging of patient content for IRB/EC Submissions.

• Works with CRO and UCB Study Team members to ensure facilitation of the study requirements into the overall design.

• Work with appropriate vendors to ensure proper eCOA translations & validation has been completed

Assists with the overall support and device enablement with the overall Launch, Run, Support lead to ensure proper and timely enablement of the team.