/Companies

Concordare Trials

Techstars '26

New York City, US · 7 employees on LinkedIn · 5 known investors

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Concordare provides infrastructure for clinical research by extracting trial information into a standardized protocol model and automatically generating downstream deliverables for coordinators, eliminating manual documentation work across systems.

Also known as Concordare · Concordare Trials Inc.

Founders & leadership

ZSZach S.
Zach S.CEO and Founder

Investors · 5

Also in the syndicate · 1

Individual investors

Company profile

researched Sep 2026

Concordare Trials is a New York-based clinical research software company that converts static clinical trial protocol documents into a structured, machine-readable format it calls the Clinical Trial Protocol Model (CTPM). Protocols, which the company describes as frequently exceeding 300 pages, are today read and reinterpreted by many separate teams at hospitals, vendors and software groups, each of whom rebuilds the same study logic into calendars, checklists and operational documents. Concordare's stated aim is to make the protocol itself interoperable so that one extraction drives the downstream operational artifacts.

The product ingests study design PDFs through an AI conversion engine (referred to as Apta on the company site, and as the Concordare Suite in press announcements) and produces a protocol-specific CTPM. From that model the platform generates visit-by-visit source documents and procedure worksheets, electronic data capture (EDC) builds including forms, fields and validation/edit-check rules, clinical trial management system (CTMS) configurations such as milestones, site setup and visit schedules, and billing grids/schedules of events and costs. The company states AI is used only for extraction and that every CTPM is reviewed and approved by the customer's team before any output is generated. A February 2026 interview also references a site-facing product called Concordare Opus.

The company positions itself against clinical trial software that manages studies after operational setup has already occurred or that is tied to a single sponsor ecosystem, and says its format is designed to work across any sponsor, site and downstream system so a site can apply it across all of its studies.

Founding story

Sawaged states he started the company after experiencing the problem directly in clinical operations at NYU Langone's Perlmutter Cancer Center, where he observed teams repeatedly rebuilding the same protocol logic across different tools, and concluded the protocol itself should be digital and reusable. He trained in biomedical informatics at NYU, which he describes as where the early foundation for the company was shaped.

Business model

Software sold to clinical research sites as well as sponsors and CROs, with the website offering separate entry paths for sites and for sponsors/CROs. The company describes an enterprise motion involving pilots with tightly scoped success metrics, implementation processes for large institutions, onboarding, security review and training.

Traction

Live pilot deployments including Rutgers University, described as a longtime partner using the platform across multiple teams; implementation processes being finalized with NYU Langone and Memorial Sloan Kettering; the company states it is contracting with additional institutions nationwide. The company claims study activation acceleration of six to eight weeks.

Latest developments

In August 2026 the company announced a funding round led by Surface Ventures with participation from Techstars, Innovation Works, Gaingels and individual investors, to fund product development, team expansion and site partnership growth. The team said it expected to add experienced clinical and product hires and had assembled an advisory bench with clinical development and product experience.

▸Full profile — market position, technology, go-to-market, geography, history, risks & controversies

Market position

Positions itself as protocol-centric infrastructure that operates earlier in the study lifecycle than systems that track or manage work after operational setup, and as sponsor-agnostic rather than tied to a single sponsor ecosystem or monolithic platform.

A protocol-level, system-agnostic data model intended to work across any sponsor, site and downstream system, allowing sites to adopt it across all studies rather than one study at a time, and reducing protocol interpretation work rather than only tracking it. EDC builds and source documents are generated from the same model, keeping them aligned, and outputs require human validation of the model first.

Technology

An AI conversion engine converts study design PDFs into the Clinical Trial Protocol Model (CTPM), a system-agnostic structured digital representation of a trial. The CTPM acts as a single source of truth from which source documents, EDC databases (forms, fields, validation rules), CTMS configurations and billing/cost schedules are generated. AI is used exclusively for extraction, with a human-in-the-loop review and approval step before outputs are produced.

Go-to-market

Site-first approach designed around existing research coordinator workflows, entering institutions via narrowly scoped pilots with defined success metrics before broader implementation; the company reports navigating long, multi-stakeholder enterprise sales cycles and institutional security and compliance reviews. Funding is being applied to product development, team expansion and growth of the site partnership network.

Clinical research sites (research coordinators and site operations teams), academic medical centers, plus sponsors and CROs.

Geography

Headquartered in New York; partner network described as U.S. academic medical centers, with contracting under way with additional institutions nationwide.

History

Founder Zach Sawaged worked for four years at NYU Langone's Perlmutter Cancer Center and, per press coverage, spent about a decade across clinical research sites, sponsors and technology vendors including NYU Langone, Amgen, Johnson & Johnson, Takeda and Veeva before founding the company. He recruited engineer Nathan Maher after working together for a couple of months. By February 2026 the company reported live pilots including Rutgers and was finalizing implementation processes for NYU Langone and Memorial Sloan Kettering, and participated in the NYU Entrepreneurs Challenge. A funding round led by Surface Ventures was announced on 25 August 2026.

Risks & controversies

The company cites challenges in meeting enterprise security, compliance and integration requirements, variability of clinical research workflows across institutions, institutional caution about changes touching patient-facing operations or regulatory processes, and long multi-stakeholder sales cycles. Reported efficiency figures such as the $25 million per-study configuration cost and six-to-eight-week activation savings are company estimates.

Compiled by commissioned research from 8 cited public sources — announcements, filings, and press listed under research sources below.

Key figures

latest reported
Estimated cost of manual system configuration per study (company estimate)Aug 2026$25M
HeadcountAug 20267
Study activation acceleration (company claim)Aug 20266-8 weeks

Company-reported or press-reported figures, each dated to when it was claimed — not independently audited.

Timeline · 3

launches, deals, and filings
Aug 2026
Concordare Trials closes funding round led by Surface Ventures

Concordare Trials announced the close of a funding round led by Surface Ventures, with participation from Techstars, Innovation Works, Gaingels and individual investors. Proceeds are directed to product development, team expansion and growth of the site partnership network.

source ↗

Feb 2026
Featured in NYU Stern Berkley Center venture profile ahead of the NYU Entrepreneurs Challenge

Concordare Trials, founded by Zach Sawaged (GSAS '20) with team member Nathan Maher, was profiled by the NYU Stern Berkley Center in connection with the NYU Entrepreneurs Challenge.

source ↗

Feb 2026
Live pilot with Rutgers University

The company reported live pilot validation at Rutgers, demonstrating conversion of a protocol into a structured format driving site-facing outputs; a later announcement described Rutgers as a longtime partner using the platform across multiple teams.

source ↗

Dated company events from announcements, filings, and press; legal rows summarize public dockets and regulator releases.

▸Research sources · 8

primary sources listed

8 public sources were cited for this profile; the first-party ones are listed here.

Frequently asked questions

What does Concordare Trials do?
Concordare Trials converts clinical trial protocol PDFs into a structured digital model that generates EDC, CTMS and site documents.
Who founded Concordare Trials?
Concordare Trials was founded by Zach S..
Who are Concordare Trials's investors?
Concordare Trials's investors include Gaingels, Techstars, Innovation Works, Surface Ventures.
Where is Concordare Trials headquartered?
Concordare Trials is headquartered in New York City, US.