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Crio Jobs (NOW HIRING)

Crio, Inc.

Sr. Director of Sponsor Operations

$160K - $185K/yr

CRIO is a leading provider of eSource solutions for clinical research. Our platform streamlines clinical data collection and management, ensuring protocol compliance and reducing errors. By ...

Crio, Inc.

Director of Sponsor Operations

$150K - $170K/yr

CRIO is a leading provider of eSource solutions for clinical research. Our platform streamlines clinical data collection and management, ensuring protocol compliance and reducing errors. By ...

Crio, Inc.

Product Owner

$100K - $130K/yr

CRIO (Clinical Research IO) 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 ...

Crio, Inc.

Software QA Engineer II

$75K - $85K/yr

CRIO (Clinical Research IO) 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 ...

Crio, Inc.

Engineering Manager

CRIO is a leading provider of eSource solutions for clinical research. Our platform streamlines clinical data collection and management, ensuring protocol compliance and reducing errors. By ...

Accord Technologies Inc.

LABVIEW Developer

Milpitas, CA · On-site

LabView Developer Milpitas, CA Medical device domain LabView Developer Skill Matrix LabVIEW FPGA cRIO systems NI DAQ hardware hardware integration (PLCs, motors, sensors, instruments) code migration ...

RoviSys

LabVIEW Engineer

Aurora, OH · On-site

$100K - $130K/yr

Experience with NI Real-Time programming for embedded targets (cRIO, PXIe). * Ability to interact with mechanical designers and provide suggestions. * Experience with Robotics and Vision Inspection ...

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Crio information

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How much do crio jobs pay per hour?

As of Jul 25, 2026, the average hourly pay for crio in the United States is $25.47, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $29.57 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Investigator (CRIO), and why are they important?

To thrive as a Clinical Research Investigator (CRIO), you need a medical or scientific degree, thorough knowledge of clinical trial protocols, and experience in research ethics and regulations. Familiarity with electronic data capture systems, Good Clinical Practice (GCP) certification, and clinical trial management software is essential. Strong attention to detail, leadership, and effective communication set top performers apart in this field. These skills and qualifications are crucial for ensuring research integrity, patient safety, and regulatory compliance in clinical studies.

What is the difference between Crio vs Software Engineer?

CriteriaCrioSoftware Engineer
Required credentialsBootcamp certification, coding projectsBachelor's degree in CS or related field
Work environmentOnline, project-based learning platformOffice or remote software development teams
Employer and industry usageTech startups, training programsTech companies, software firms
Common search intentLearning, skill developmentEmployment, career advancement

Crio focuses on immersive coding bootcamps and project-based learning to prepare individuals for software development roles, often without requiring a traditional degree. Software Engineers typically hold formal degrees and work within established tech companies. While Crio emphasizes skill-building through practical projects, Software Engineers are employed to develop and maintain software products. Both roles are integral to the tech industry but differ mainly in training approach and employment status.

What are Crio jobs?

Crio jobs typically refer to roles at Crio, a company known for providing experiential learning platforms in technology education. These jobs can include software engineering, content development, curriculum design, business development, and support roles. Employees at Crio help create project-based learning modules, mentor students, and contribute to the growth of technology education. The work environment often emphasizes innovation, collaboration, and the development of practical industry skills. Applicants usually need a background relevant to education technology or software development.

What are some common challenges faced by Crio engineers when working on real-world projects, and how can they overcome them?

Crio engineers often work on practical, industry-relevant projects that require balancing learning with delivering results under deadlines. A common challenge is quickly adapting to new technologies and solving open-ended problems with minimal guidance. To overcome this, it's important to actively seek feedback from mentors, collaborate effectively with peers, and utilize available documentation and community resources. Embracing a growth mindset and being proactive in communication will help you navigate project roadblocks and develop industry-ready skills.
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Crio jobs near you
Infographic showing various Crio job openings in the United States as of July 2026, with employment types broken down into 96% Full Time, 3% Part Time, and 1% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $52,986 per year, or $25.5 per hour.
Sr. Director of Sponsor Operations

Sr. Director of Sponsor Operations

Crio, Inc.

Remote

$160K - $185K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago

Job description

CRIO is a leading provider of eSource solutions for clinical research. Our platform streamlines clinical data collection and management, ensuring protocol compliance and reducing errors. By eliminating paper binders and automating workflows, we help clinical trial sites and sponsors save time and money, improve data quality, and enhance patient safety. Our digital-first, site-centric approach supports virtual, hybrid, and traditional study structures, making clinical trials more efficient and effective.
Founded in 2015 by a clinical trial site owner seeking to improve his own business, today CRIO is the industry leader in site eSource with a fast-growing presence serving sponsors and CROs. CRIO is in use on 6000+ protocols at more than 2500 sites in 30 countries. In fact, the strength of our site community drives our growth which is why we place so much value on hands-on clinical research experience.
Position Summary
The Senior Director of Sponsor Operations is responsible for building, scaling, and leading CRIO's enterprise sponsor business, including Central eSource programs across global pharmaceutical and CRO organizations.
This role owns the end to end sponsor lifecycle from initial engagement through multi study execution and long term expansion. The Head of Sponsor Operations ensures consistent, high quality delivery across all enterprise sponsor programs while establishing scalable operational frameworks that enable CRIO to grow its sponsor footprint effectively.
A critical component of this role is ownership of clinical data strategy and execution across sponsor programs, including data standards, integration alignment, data quality, and regulatory compliance. This individual ensures that CRIO's eSource data is structured, mapped, validated, and delivered in a way that meets sponsor expectations and industry requirements.
Operating at the intersection of sponsor strategy, clinical operations, and technical data delivery, this role partners closely with Product, Engineering, and Customer Experience to align enterprise sponsor needs with CRIO's platform capabilities and long term roadmap.
Key Responsibilities
Enterprise Sponsor Strategy and Growth
  • Own the operational strategy for all enterprise sponsor programs including Lilly, ICON, Moderna, and future enterprise accounts
  • Partner with Sales and Executive Leadership to support enterprise deal strategy, solution design, and expansion planning
  • Define scalable Central eSource operating models across sponsor organizations
  • Identify opportunities to expand sponsor adoption across additional studies, geographies, and use cases

Sponsor Portfolio Ownership and Execution
  • Own delivery across all active and planned studies within enterprise sponsor portfolios
  • Ensure consistency in execution, timelines, and quality across all sponsor engagements
  • Establish standardized workflows, templates, and delivery frameworks across sponsors
  • Drive visibility through executive level reporting on portfolio health, risks, and performance
  • Establish governance models for enterprise sponsor accounts including regular executive reviews and QBR structures
  • Serve as senior leadership point of contact for sponsor organizations
  • Lead high level sponsor discussions related to scope, timelines, data expectations, and escalations

Clinical Data Strategy and Oversight
  • Own the clinical data framework for all sponsor programs, ensuring alignment with industry standards and sponsor expectations
  • Oversee CDASH mapping, data structuring, and standardization across all studies
  • Ensure consistency and quality of data capture, validation, and downstream usability
  • Define and enforce data governance practices across sponsor portfolios
  • Oversee the alignment of eSource data with EDC systems, ensuring accurate, complete, and compliant data transfer
  • Ensure integration outputs meet sponsor requirements for data quality, structure, and format
  • Establish processes for - Data review and validation, Query management alignment with sponsor workflows, XML and structured data output review

Operational Architecture and Central eSource Design Alignment
  • Oversee enterprise Central eSource design frameworks, ensuring alignment with sponsor protocols, regulatory requirements, and site workflows
  • Define data capture logic, workflow structures, and role based access models across studies
  • Drive standardization across study configuration, amendment processes, and UAT strategies
  • Establish repeatable deployment models that balance flexibility with scalability
  • Identify and champion opportunities to embed AI-driven automation across sponsor workflows, including Central eSource design configuration, data validation, query management, and amendment processing
  • Partner with Product and Engineering to define enterprise requirements for AI-assisted capabilities, such as intelligent data capture, protocol deviation detection, and EDC integration quality checks
  • Stay ahead of emerging AI applications in clinical data and eSource, translating sponsor needs and operational patterns into actionable input for CRIO's AI product roadmap

Integration and Technical Delivery Alignment
  • Partner with Product and Engineering to define and prioritize enterprise integration requirements across EDC, CTMS, eRegulatory, and external systems
  • Ensure data integrity and consistency across all integration points
  • Serve as executive escalation point for complex technical, data, and integration challenges

Cross Functional Leadership and Alignment
  • Lead coordination across Sponsor Operations, Central eSource design, Data Migration, Product, Engineering, and Customer Experience teams
  • Ensure alignment between sponsor requirements and internal delivery capabilities
  • Identify and resolve systemic gaps across workflows, data handling, and handoffs
  • Partner with Product Leadership to influence roadmap priorities based on enterprise data and integration needs
  • Drive accountability across all functions involved in sponsor delivery
Qualifications
Required
  • 10+ years of experience in clinical research technology, data management, sponsor operations, or clinical trial systems
  • 5-7+ years of operational team and/or personnel management
  • Strong background in clinical data management, including:
  • CDISC standards (CDASH, USDM, SDTM, etc.)
  • Data mapping and transformation
  • Data validation and quality processes
  • Proven experience managing enterprise sponsor or CRO relationships across multiple studies or programs
  • Deep understanding of clinical trial workflows, site operations, and regulatory requirements
  • Experience working with eSource, EDC, CTMS, or related clinical platforms
  • Demonstrated ability to lead complex, data intensive, cross functional programs
  • Exceptional communication and executive presence

Preferred
  • Exposure with Central eSource concept models or similar sponsor site integrated workflows
  • Familiarity with HL7 FHIR, API based integrations, or structured data exchange models
  • Experience overseeing data migration or large scale data transformation initiatives
  • Background in CRO, sponsor organization, or clinical technology vendor environment
  • Prior experience scaling teams in a high growth environment

Benefits & Perks:
  • Work from anywhere
  • Unlimited PTO
  • 401k company match
  • Healthcare
  • Dental
  • Vision (Company Paid 100%)
  • Life insurance
  • Professional development
  • Work From Home Expense Reimbursement

Working Conditions
This is a full-time, remote or hybrid position. Occasional travel may be required based on client timelines and sponsor engagement needs. Flexibility may be required to align with sponsor and project schedules across time zones.
Equal Employment Opportunity:
CRIO is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions are made based on qualifications, merit, and business need without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability status, age, or any other basis protected by federal, state, or local law.
Disability Accommodation Statement:
We are committed to providing reasonable accommodations to individuals with disabilities in the application and interview process. If you require accommodation to participate in the application process, please contact Human Resources to request assistance.
Salary Range: $160,000 -- $185,000

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