eSource Platform Design Lead

Science 37; Morrisville (NC); On-site; USD 110,000 - 150,000; Full time

Job summary

Science 37 is seeking a Clinical Study Design Manager in Morrisville, NC to define eSource platform specifications and data capture requirements, bridging protocol needs with implementation. You will oversee offshore build teams to ensure quality and timely delivery across the study lifecycle.

You will serve as SME for system capabilities, collaborate with clients and internal teams, and drive standardization through templates and libraries while maintaining QA and project timelines.

Qualifications

• 3+ years in clinical research or life sciences, including CRF/ePRO design.
• 2+ years CRIO platform experience.
• Bachelor’s degree or equivalent in health science.
• Extensive knowledge of the clinical research development process.
• Experience in fast-moving growth-oriented company and adaptability.

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 all platform design and build milestones are met according to project timelines and technical specifications.
• Serve as the SME for system capabilities, data capture configuration, and the validation of the eSource Platform.
• Drive efficiency by implementing standard templates and libraries and contributing to streamlined building and QC processes.
• Collaborate in cross-functional project teams with Clients, Site Operations Managers, and internal staff to document data collection requirements.
• Create and maintain project timelines, monitor progress of all design activities, and stay accountable for quality metrics and KPIs.
• Lead build, testing, and implementation of direct data capture services, ensuring system integration and user acceptance testing to meet quality deliverables.
• Participate in review and revision of SOPs and work instructions.
• Train and mentor Platform Build Managers and support specialists to foster excellence and speed.
• Oversee and perform user access management for all Science 37 eSource platforms.
• Partner with Clinical Operations and Data Management to provide input on protocol design and post-production changes.
• Build and maintain relationships with clients, sponsors, and vendors to ensure project success.

Skills

CRF/ePRO design

CRIO platform experience

clinical research

data capture

protocol involvement

Education

Bachelor's degree in health sciences

Job description

Science 37 is seeking a Clinical Study Design Manager in Morrisville, NC to define eSource platform specifications and data capture requirements, bridging protocol needs with implementation. You will oversee offshore build teams to ensure quality and timely delivery across the study lifecycle.

You will serve as SME for system capabilities, collaborate with clients and internal teams, and drive standardization through templates and libraries while maintaining QA and project timelines.