C

CRIO

Enterprise clinical trial data capture platform

Director of Sponsor Operations - Study Design & Data Management

Full-TimeUpdated on 10/25/2026
$150k - $170k
Expert
Remote in USA
RemoteWork from anywhere within the United States.
Biology & BiotechClinical Research Operations

About the job

Requirements
  • At least 5 years of experience in clinical research technology, data management, sponsor operations, or clinical trial systems.
  • Strong background in clinical data management, including CDISC standards (CDASH, USDM, SDTM, etc.), data mapping and transformation, and 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.
Responsibilities
  • Lead the overall strategy and execution of CRIO’s Sponsor Operations function, overseeing delivery across all enterprise and strategic sponsor programs.
  • Establish and enforce operational standards, ensuring all sponsor projects adhere to CRIO’s quality, efficiency, and compliance expectations.
  • Translate organizational goals into measurable outcomes, defining KPIs and success metrics for sponsor delivery performance, client satisfaction, and scalability.
  • Partner with executive leadership to align sponsor operations with company growth, product roadmap, and market positioning.
  • Oversee multiple enterprise sponsor portfolios, ensuring programs are delivered on time, within scope, and with high quality.
  • Supervise and mentor Sponsor Program Managers in managing end-to-end delivery, risk mitigation, and escalation management.
  • Ensure consistent study execution by aligning Central eSource design, Implementation, Site Enablement, and Sponsor Project Manager teams under shared delivery frameworks.
  • Drive continuous improvement through standardized documentation, operational playbooks, and cross-functional reporting systems.
  • Develop scalable delivery models, workflow frameworks, and standard operating procedures that enhance consistency across sponsor engagements.
  • Identify process bottlenecks and lead strategic initiatives to optimize handoffs between functional areas, including Product, Engineering, CX, and Data.
  • Champion automation and tooling initiatives that improve visibility, accountability, and client transparency.
  • Manage and optimize resource allocation across study operations functions to meet demand and delivery targets.
  • Serve as the senior escalation point for enterprise sponsor relationships, driving resolution and ensuring a strong client experience.
  • Collaborate with Product and Engineering to translate enterprise feedback into roadmap priorities and platform enhancements.
  • Partner with the Data and Analytics teams to define sponsor reporting standards and provide visibility into key operational metrics.
  • Represent Sponsor Operations in strategic client meetings, governance sessions, and executive reviews.
  • Lead, mentor, and develop the Sponsor Operations team.
  • Create competency frameworks and progression paths for Sponsor Operations roles, including PMs, Operations Leads, Study Managers, and Team Leads.
  • Foster a culture of continuous improvement, empowering teams to innovate and refine delivery approaches.
  • Partner with HR and Learning teams to build onboarding, training, and certification programs for sponsor delivery excellence.
Desired Qualifications
  • Exposure to 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 a CRO, sponsor organization, or clinical technology vendor environment.
  • Prior experience scaling teams in a high-growth environment.

About the company

CRIO provides an integrated health tech platform for clinical trials, unifying data capture and regulatory workflows through eSource that feeds directly into electronic data capture (EDC) for remote monitoring and real-time data review. It captures data once at a single point and uses autofill and data validation to reduce protocol deviations and avoid re-entry, while offering modules like patient scheduling, recruitment, and financial management. Its differentiators include leadership in eSource, a single platform that serves both sites and sponsor organizations, and built-in compliance with 21 CFR 11, ICH-GCP, GDPR, and HIPAA. CRIO’s goal is to improve the quality and speed of trials and enable patient-centric data access from anywhere, so trials can be conducted where patients are.

Company Size

51-200

Company Stage

Late Stage VC

Total Funding

$19M

Headquarters

Boston, Massachusetts

Founded

2015

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Simplify's Take

What believers are saying

  • Medidata said one in four US chronic-condition sites now use CRIO’s ecosystem.
  • On September 2026, CRIO added Todata SiteGrades for real-time site analytics.
  • CRIO’s September 2026 blog cadence signals active product marketing and customer education.

What critics are saying

  • CRIO’s differentiation depends on Medidata and other partners like Inato, creating platform leverage risk.
  • Clinical research platforms from Veeva and Medidata can commoditize eSource and CTMS workflows.
  • Stalled site adoption turns Riverside’s capital into a costly bridge, not growth fuel.

What makes CRIO unique

  • CRIO’s March 2026 Medidata integration automates source-to-EDC transfer across 2,500 sites.
  • Its Central eSource standardizes templates centrally while preserving site-specific workflows.
  • Lightship adopted CRIO in February 2026, proving repeatable operations for multi-site networks.

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Benefits

  • Remote Work Options
  • Unlimited Paid Time Off
  • 401(k) Company Match
  • Health Insurance
  • Dental Insurance
  • Vision Insurance
  • Life Insurance
  • Professional Development Budget
  • Home Office Stipend

Growth & Insights and Company News

6 month growth

-2%

1 year growth

0%

2 year growth

-1%
Associated Press
Oct 13th, 2026
CRIO launches AI eSource Builder, cutting study build time by four hours per trial

CRIO, a provider of eSource technology for clinical research, has launched AI eSource Builder, which drafts a research site's eSource study build from the protocol, supporting documents and site preferences. Early adopter sites save an average of four hours per study build. Sites upload protocols and electronic case report forms. The tool reads the Schedule of Assessments and generates visits, windows and procedure templates, guided by more than 150 build rules that each site can adjust. Study designers review and refine every draft before it goes live. The tool uses only study design documents, so no electronic protected health information is involved. A Tufts Center for the Study of Drug Development study found at least 80% of sites say preparing source documents for complex trials takes more than 21 hours.

PR Newswire
Jan 21st, 2026
CRIO partners with Todata to offer clinical research sites real-time performance analytics

CRIO, a leader in eSource technology for clinical research, has partnered with Todata Analytics to integrate SiteGrades as an analytics solution within CRIO's Partners Programme. The collaboration enables clinical research sites to access real-time performance dashboards without per-user fees or technical implementation requirements. SiteGrades provides sites with dashboards tracking enrollment performance, exam room utilisation and financial metrics. The platform can connect financial systems, HR platforms and other data sources to deliver comprehensive operational insights. It includes Tod AI, Todata's compliant artificial intelligence layer, allowing teams to query complex data instantly. CRIO customers can access the integration immediately. Both platforms operate within HIPAA-compliant frameworks. CRIO has been providing eSource technology since 2015, whilst Todata Analytics was founded in 2017.

Business Wire
May 21st, 2024
CRIO Secures Major Investment for Expansion

CRIO, Inc., a leading provider of eSource and eClinical technologies, has received a significant investment from The Riverside Company, a global private equity firm. This investment will support CRIO's continued expansion and enhancement of its eClinical platform, which streamlines clinical trial processes and improves data quality. Co-CEOs Raymond Nomizu and Jonathan Andrus highlighted the benefits of Riverside's financial support and industry expertise in achieving CRIO's goals.

Climedo
Mar 11th, 2024
Trial Physician Survey: Status Quo in Clinical Research

In the fall of 2023, Climedo Health GmbH collaborated with Siteworks Clinical Research to conduct a survey aiming to understand trial physicians' perspectives on clinical trials and capture the current state of clinical research.

PR Newswire
Nov 28th, 2023
Are Regulators Driving Or Impeding Innovation In Clinical Trials? Upcoming Webinar Hosted By Xtalks

Internal quality assurance (QA) and regulatory teams can be a hold-up when they rely on historical practices and personal preference rather than current regulatory guidance in assessing the feasibility and risks of implementing new and innovative solutions to clinical trial challenges. .