eSource Study Design Lead — Global Build & Quality

Science 37; Raleigh (NC); On-site; USD 120,000 - 170,000; Full time

Job summary

Science 37 is seeking a Clinical Study Design Manager to define eSource platform specifications for studies, bridging protocol requirements with implementation and overseeing offshore build teams to meet milestones.

You will collaborate with clients and internal staff, contribute to protocol design input with Clinical Operations and Data Management, and mentor Platform Build Managers. A strong background in CRF/ePRO design and CRIO platform experience is required.

Qualifications

• 3+ years of experience in clinical research or life science industry, including at least 3 years in design of CRF/ePRO or other clinical trials database capture software.
• 2+ years of CRIO platform experience is required.
• Bachelor’s degree or equivalent experience in the health science field.

Responsibilities

• Define and specify eSource design requirements for assigned studies, collaborating with internal teams and clients to ensure protocol alignment.
• Work with offshore teams to ensure platform design and build milestones are met according to timelines and specifications.
• Serve as the SME for system capabilities, data capture configuration, and validation of the eSource Platform.
• Lead the build, testing, and implementation of direct data capture services, ensuring system integration and user acceptance testing to meet quality deliverables.
• Train and mentor Platform Build Managers and support specialists to foster a culture of excellence and speed.

Skills

CRF/ePRO design

Offshore coordination

Strong communication

Project management

Education

Bachelor's degree in health science

Tools

CRIO platform

Job description

Science 37 is seeking a Clinical Study Design Manager to define eSource platform specifications for studies, bridging protocol requirements with implementation and overseeing offshore build teams to meet milestones.

You will collaborate with clients and internal staff, contribute to protocol design input with Clinical Operations and Data Management, and mentor Platform Build Managers. A strong background in CRF/ePRO design and CRIO platform experience is required.