eSource Platform Design Lead for Clinical Studies

Science 37; Boston, Northern (MA, KY); Hybrid; USD 120,000 - 180,000; Full time

Job summary

Science 37 is seeking a Clinical Study Design Manager to define eSource platform specifications and oversee the full design-to-implementation lifecycle. You will coordinate offshore build teams, ensure quality standards, and partner with clinical operations to align protocols with data capture requirements.

The role requires 3+ years in clinical research design (CRF/ePRO) and 2+ years with CRIO platforms. Strong communication and leadership are essential for success in a fast-paced, global team.

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.
• Extensive knowledge of the clinical research development process.
• Experience in a fast-moving, growth-minded company with adaptable requirements.
• Understanding of drug development process and regulatory guidelines.
• Strong written and verbal communication skills.
• Ability to lead cross-functional teams and coordinate with clients, vendors and internal teams.
• Excellent time management and attention to detail.

Responsibilities

• Define and specify eSource design requirements for assigned studies, collaborating with internal teams and clients.
• Work with offshore teams to meet milestones per timelines and specifications.
• Serve as SME for system capabilities and data capture configuration.
• Drive efficiency by implementing standard templates and libraries for faster build and QC.
• Collaborate in cross-functional project teams to document data collection requirements.
• Create and maintain project timelines and monitor progress against KPIs and quality metrics.
• Lead build, testing, and implementation of direct data capture services and system integration.
• Review and revise SOPs and work instructions to improve processes.
• Train and mentor Platform Build Managers and support specialists.
• Oversee user access management for all Science 37 eSource platforms.
• Partner with Clinical Operations and Data Management for protocol design input.
• Build and maintain relationships with clients, sponsors, and vendors to ensure project success.

Skills

Clinical research

CRF/ePRO design

CRIO platform

Team leadership

Communication skills

Offshore coordination

Problem solving

Time management

Education

Bachelor’s degree in health science

Tools

Microsoft Office

Google applications

Job description

Science 37 is seeking a Clinical Study Design Manager to define eSource platform specifications and oversee the full design-to-implementation lifecycle. You will coordinate offshore build teams, ensure quality standards, and partner with clinical operations to align protocols with data capture requirements.

The role requires 3+ years in clinical research design (CRF/ePRO) and 2+ years with CRIO platforms. Strong communication and leadership are essential for success in a fast-paced, global team.