Enterprise Solutions & Study Operations Lead

CRIO

Remote
Base: $90,000 - $130,000; bonus/equity: not specif...
Remote
Clinical research technology expertise
Multi-study sponsor portfolio management
Esource operational excellence
CRIO is a health tech company helping pharma, biotech, research sites, and academic research centers streamline regulatory workflows with one system and a single source of clinical data capture

Job Summary

  • CRIO is a health tech company helping pharma, biotech, research sites, and academic research centers streamline regulatory workflows with one system and a single source of clinical data capture.
  • The Enterprise Solutions & Study Operations Lead serves as the operational and strategic backbone of CRIO’s Central eSource sponsor programs, ensuring clarity, consistency, and accountability across multi-study portfolios.
  • This role involves leading sponsor engagement, overseeing study design and operational architecture, coordinating integration development, managing internal resources, and driving change management and project governance.

Matching Summary

CRIO is a health tech company helping pharma, biotech, research sites, and academic research centers streamline regulatory workflows with one system and a single source of clinical data capture.

Salary

Base: $90,000 - $130,000; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • clinical research technology expertise
  • multi-study sponsor portfolio management
  • eSource operational excellence
  • stakeholder relationship management
  • clinical trial operations knowledge
  • integration architecture coordination
  • regulatory data standards familiarity

Nice-to-have

  • mentorship and training skills
  • cross-functional team orchestration
  • change management proficiency
  • communication with technical and non-technical audiences
  • process improvement and governance
  • experience with HL7 FHIR and API integrations

Key Requirements

  • 7+ years clinical research technology experience
  • experience managing multi-stakeholder clinical programs
  • strong understanding of GCP and regulatory requirements
  • familiarity with CDASH standards and study build documentation
  • exceptional communication and facilitation skills
  • bachelor’s degree in relevant field preferred

Work Rights

Not specified

Tailored Resume

Cover Letter