Global eSource Study Design Lead

Science 37; Boston (MA); On-site; USD 120,000 - 180,000; Full time

Job summary

Science 37 in Boston seeks a Clinical Study Design Manager to define eSource platform specifications and requirements across studies, coordinating with offshore teams to meet milestones and quality standards. The role spans design through implementation, ensuring smooth integration and robust data capture.

The candidate serves as SME for data capture configuration, drives templates and QC, mentors build managers, and partners with Clinical Operations and Data Management to implement protocol

Qualifications

• 3+ years of experience in clinical research or life sciences, including CRF/ePRO design.
• 2+ years of CRIO platform experience.
• Bachelor’s degree or equivalent in health science.
• Extensive knowledge of clinical research development process.
• Experience in a fast-moving, growth-minded company adapting to changing requirements.
• Understanding of drug development and regulatory guidelines.
• Ability to create and review protocols and assess project success.
• Experience building and guiding organizational teams with clear direction.
• Proactive problem-solving and follow-through.
• Strong written and verbal communication and presentation skills.
• Ability to communicate with both technical and non-technical audiences.
• Ability to maintain positive sponsor, vendor, and internal relationships.
• Excellent time management, attention to detail, and strategic thinking.
• Proficiency with Microsoft Office, Google apps, and electronic clinical tech.
• Fosters teamwork, cooperation, and flexibility to get work done.

Responsibilities

• Define and specify eSource design requirements for assigned studies with protocol alignment.
• Coordinate with offshore teams to meet milestones per timelines and specs.
• Serve as SME for system capabilities, data capture configuration, and platform validation.
• Implement templates and libraries to drive efficiency and QC improvements.
• Collaborate with cross-functional teams to document data collection requirements.
• Create and maintain project timelines; monitor design progress and KPIs.
• Lead build, testing, and implementation of direct data capture services.
• Review and revise SOPs and work instructions.
• Train and mentor Platform Build Managers and support staff.
• Oversee user access management for all eSource platforms.
• Partner with Clinical Ops and Data Management on protocol design and post-production changes.
• Build relationships with clients, sponsors, and vendors to ensure project success.

Skills

Clinical research

CRIO platform experience

Documentation design

Communication skills

Team leadership

Education

Bachelor’s degree in life sciences or health field

Job description

Science 37 in Boston seeks a Clinical Study Design Manager to define eSource platform specifications and requirements across studies, coordinating with offshore teams to meet milestones and quality standards. The role spans design through implementation, ensuring smooth integration and robust data capture.

The candidate serves as SME for data capture configuration, drives templates and QC, mentors build managers, and partners with Clinical Operations and Data Management to implement protocol