---
title: 'Clinical Technology Consultant at Suvoda'
canonical: 'https://feeny.ai/job/clinical-technology-consultant-suvoda-conshohocken-temdrc9dq7f6'
type: 'job'
last_seen: '2026-09-08'
---

# Clinical Technology Consultant at Suvoda

- **Company:** Suvoda
- **Location:** Conshohocken, PA
- **Posted:** 2026-08-24
- **Last confirmed live:** 2026-09-08
- **Apply:** https://www.suvoda.com/careers/job-openings?gh_jid=8742001002

## Job description

Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease.

Supporting clinical trials means supporting unique experiments that are inherently complex, high-stakes, and dynamic. It is imperative that Suvoda staff working with clients, end-users, or the systems that client and end-users interact with understand the clinical trial industry, regulations, Suvoda’s software products and processes, and especially the specificities of the unique trial in question before taking any actions they may alter the data of the system in question.

Responsibilities:

- Work on a cross-functional project team responsible for the delivery of Interactive Response Technology (IRT) for randomization and drug supply management;
- Design the IRT solution to meet the study requirements based on the clinical protocol, the Suvoda proposal/executed work order, and discussions with the client;
- Consult with clients to best understand their business requirements and act as a trusted advisor for translating these requirements into Suvoda’s software;
- Accurately and completely document all requirements in the specification template(s);
- Lead the internal team review of the draft specifications; main point of contact for the internal team for all IRT design related questions throughout the build process;
- Lead the client review of the IRT specifications and supporting documents, making any required updates and obtaining both client and internal approval by the agreed upon milestone date;
- Responsible for the UAT plan, test scripts, and coordinate all required data setup for client UAT;
- Primary point of contact for design questions (internally and externally) during the system build process;
- Lead client UAT of the IRT system, tracking any required fixes or updates; work with the project manager to determine timelines for any system updates required;
- Support any re-design of the IRT system or implementation of new features in an IRT system during the maintenance period • Identify and assist with the implementation of process improvements for the services department;
- Assist the product team with the design and development of new features by providing feedback based on client requests and project experience
- Travel to client sites to attend meetings and conduct user training sessions;
- Assist the customer care team with providing support to system users (as required) via the telephone and email;
- Assist with the training of new staff members on the Suvoda product and processes;
- Perform continuous risk assessments throughout the project lifecycle to identify new risks and update mitigation strategies accordingly;
- Perform other related duties as required;

Requirements:

- 2-3 years of experience in a similar role;
- 1 year of experience in IRT or related field preferred;
- Bachelor's degree or equivalent experience required;
- Interpersonal and communication skills;
- Time management and organizational skills;
- Analytical and systematic thinking ability;
- Creative problem solving;
- Ability to understand technical details and translate them to non-technical users;
- Attention to detail;
- Demonstrated strong consultative skills.

## #LI-CG1

We are aware that an individual(s) are fraudulently representing themselves as Suvoda recruiters and/or hiring managers. Suvoda will never request personal information such as your bank account number, credit card number, drivers license or social security number — or request payment from you — during the job application or interview process. Any emails from the Suvoda recruiting team will come from a @suvoda.com email address. You can learn more about these types of fraud by referring to [this FTC consumer alert](https://consumer.ftc.gov/consumer-alerts/2023/05/scammers-are-hijacking-job-ads-heres-how-spot-fakes).

As set forth in Suvoda’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.

If you are based in California, we encourage you to read this important information for California residents linked [here](https://www.suvoda.com/california-applicant-privacy-notice-and-policy).

## About Suvoda

## Company Overview
- **One-liner**: Suvoda provides a patient-centric, real-time clinical trial technology platform that streamlines workflows for sponsors, CROs, sites, and patients.
- **Entity Type**: Private (private equity-backed; merged with Greenphire in 2025)
- **Headquarters**: Philadelphia, Pennsylvania, USA (with offices in Bucharest, Tokyo, Barcelona, and other global locations)
- **Founded**: 2013
- **Founders**: Jagath Wanninayake (CEO)

## Core Business
- **Primary industry**: Clinical trial technology (life sciences / healthcare IT)
- **Target customers**: Pharmaceutical sponsors, contract research organizations (CROs), clinical trial sites, and patients
- **Mission / purpose**: “Trial Wisely” – empowering confident decisions and calm action during mission-critical moments of clinical trials.

## Products & Services
Suvoda offers a comprehensive, modular platform with eight integrated products:
- **IRT / RTSM (Interactive Response Technology / Randomization and Trial Supply Management)**: Market-leading randomization and supply chain management for complex trials, now with agentic capabilities to reduce kickoff-to-UAT to as little as two weeks.
- **eCOA (Electronic Clinical Outcome Assessment)**: Collects patient-reported outcomes and clinician-reported data electronically.
- **eConsent**: Digital informed consent management.
- **ePatient**: A single intuitive app for patients to schedule visits, submit receipts, receive payments, answer questionnaires, view travel details, and get reminders.
- **Greenphire Patient Payments**: Streamlined, compliant patient reimbursement and incentive payments.
- **Greenphire Travel**: End-to-end travel logistics and booking for trial participants.
- **Site Payments & Budget Tools**: Tools to manage site payments and trial budgets.

All products are part of the unified Suvoda Platform, synchronizing data and activity across users.

## Market Standing
- **Valuation / Market Cap**: Not publicly disclosed (private company)
- **Key Metric**: Over 2,000 clinical trials conducted; 1,000+ clients; 6,000+ trial sites in 115+ countries; $3 billion in payments processed; 65% of trials in oncology, rare disease, and CNS.
- **Notable Investors / Partners**: Backed by a leading private equity firm (acquired in 2021); merged with Greenphire in 2025.
- **Growth Signals**: Surpassed 2,000 trials; expanded to offices in Tokyo and Barcelona; holds 5 patents recognizing technology innovation; rapid product expansion (eCOA, ePatient, Greenphire suite).

## Competitive Advantages
- **Comprehensive platform**: Single vendor for IRT, eCOA, eConsent, patient payments, and travel – reducing integration complexity for sponsors.
- **Agentic RTSM**: AI-driven automation that dramatically shortens deployment timelines (kickoff to UAT in as little as two weeks).
- **Patient-centric design**: ePatient app unifies all patient touchpoints, improving retention and experience.
- **Domain expertise**: Deep specialization in high-stakes, complex trials (oncology, rare disease, CNS) with a track record of FDA approvals (34% of trials that earned FDA approval since 2024 ran on Suvoda).
- **Global scale**: 115+ countries supported, with local offices in North America, Europe, and Asia.

## Strategic Focus
- **Platform expansion**: Continuing to integrate and enhance the modular suite (eCOA, ePatient, Greenphire) to offer end-to-end trial orchestration.
- **AI & automation**: Further developing agentic capabilities in RTSM and other products to accelerate trial setup and decision-making.
- **Patient experience**: Deepening the focus on simplifying the patient journey to improve enrollment and retention.
- **Global growth**: Expanding office footprint and client base in Asia and Europe.

## Why Work Here
- **Culture**: Collaborative, mission-driven environment with small teams, open doors, and approachable leadership. Emphasis on “grit” – acting fast, managing risk, and helping each other in a high-stakes industry.
- **Hybrid work**: Flexible work environment allowing remote, office, or hybrid arrangements based on team needs.
- **Onboarding**: “Suvoda University” provides best-in-class onboarding with interactive courses, expert facilitators, and a 1:1 mentor.
- **Growth**: Opportunity to work on complex, meaningful problems that directly impact patient health; strong investment in employee development and cross-functional learning.
- **Values**: Shared commitment to learning, growth, service, and bringing wisdom and calm to critical moments.
- **Hiring process**: Transparent, quick application (5-10 minutes), thoughtful evaluation, and clear communication throughout.

## Sources
1. [Suvoda Website – Home](https://www.suvoda.com/)
2. [Suvoda – About / Company](https://www.suvoda.com/company)
3. [Suvoda – Careers](https://www.suvoda.com/careers)
4. [Suvoda – Working at Suvoda](https://www.suvoda.com/careers/working-at-suvoda)
5. [Suvoda – Job Openings (Greenhouse)](https://www.suvoda.com/careers/job-openings)

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