Full-Time

Technical Consultant

Posted on 2/21/2025

Suvoda

Suvoda

501-1,000 employees

Software solutions for managing clinical trials

Enterprise Software
Healthcare

Junior, Mid

Conshohocken, PA, USA

Category
IT Project Management
IT Support
IT & Security

You match the following Suvoda's candidate preferences

Employers are more likely to interview you if you match these preferences:

Degree
Experience
Requirements
  • Bachelor's degree or equivalent experience required
  • 2 years of experience in IRT or related field preferred
  • Interpersonal and communication skills
  • Time management and organizational skills
  • Analytical thinking
  • Ability to understand technical systems and perform troubleshooting
  • Creative problem solving
  • Attention to detail
Responsibilities
  • Work with assigned clients and project teams responsible for the delivery of Interactive Response Technology (IRT) for randomization and drug supply management
  • Responsible for overall maintenance for the team’s IRT systems, including oversight of the support process, identification and mitigation of potential issues/risks, and working with the client and other vendors to ensure success using the Suvoda IRT system
  • Lead implementation of system change controls for studies during maintenance phase
  • Manage the design of study data integration specifications between the IRT system and other eClinical solutions
  • Create data diagnostics plans for each of the team’s IRT systems and ensure that data diagnostics are completed on time per the plan
  • Create and maintain the study FAQ documents, used by the customer care team to handle support inquiries and issues
  • Responsible for the system training materials including manuals, walk through videos, and presentations
  • Work with the client study team to setup the IRT system data upon system go-live
  • Primary escalation point for the Suvoda Customer Care team on complex support issues requiring input from the project team to resolve; troubleshoot escalated issues and identify resolutions
  • Create and distribute support and maintenance reports for each of the team’s IRT systems to both internal Suvoda team members and the client’s study teams, as required
  • Proactively identify trends in support data and determine the root cause for repeated/frequent support issues; work with the Project Manager and other team members as required to identify and implement solutions
  • 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 in multiple countries via the telephone and email
  • Assist with the training of new staff members on the Suvoda product and processes
  • Perform other related duties as required
Desired Qualifications
  • 2 years of experience in IRT or related field preferred

Suvoda offers software solutions for managing complex clinical trials, primarily through its Interactive Response Technology (IRT) system. This system helps with patient randomization, drug supply management, and data collection, and is designed to be modular for quick adaptation to various study requirements. Operating on a software as a service (SaaS) model, Suvoda provides ongoing support and additional services like virtual trial solutions, which are essential for maintaining trials during disruptions like the COVID-19 pandemic. The company's goal is to simplify the clinical trial process, enabling clients to bring new treatments to market more efficiently.

Company Size

501-1,000

Company Stage

Seed

Total Funding

$38.9M

Headquarters

Conshohocken, Pennsylvania

Founded

2012

Simplify Jobs

Simplify's Take

What believers are saying

  • Suvoda's ePatient product enhances patient experience by unifying payments and appointments.
  • The company's 30% growth in 2023 indicates strong market acceptance of its platform.
  • Suvoda's low-code/no-code approach speeds up eCOA questionnaire creation and deployment.

What critics are saying

  • Emerging low-code/no-code platforms could erode Suvoda's market share.
  • Decentralized clinical trials may strain Suvoda's resources to integrate remote technologies.
  • SaaS model reliance exposes Suvoda to potential revenue fluctuations from subscription changes.

What makes Suvoda unique

  • Suvoda's IRT system offers rapid startup times, sometimes as short as four weeks.
  • The company's modular software adapts quickly to complex clinical trial requirements.
  • Suvoda's eCOA and SQDL tools accelerate questionnaire deployment, reducing traditional bottlenecks.

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Benefits

Remote Work Options

Growth & Insights and Company News

Headcount

6 month growth

-1%

1 year growth

0%

2 year growth

-2%
Pharmaceutical Technology
Nov 15th, 2024
Patient experience in the spotlight at Clinical Trials in Oncology Europe 2024

It follows after Suvoda launched its own purpose-built software platform designed to provide a seamless way for drug trial sponsors and sites to manage data across sites.

PR Newswire
Nov 14th, 2024
Suvoda Erhält Us-Patent Für Seine Ecoa-Softwarearchitektur

Der Low-Code- und No-Code-Ansatz beschleunigt den Entwurf und die Bereitstellung von eCOA-Fragebögen, indem er die Erstellung, Lizenzierung und Lokalisierung von Fragebögen aus dem kritischen Pfad nimmt. PHILADELPHIA, 14. November 2024 /PRNewswire/ – Suvoda, ein weltweit tätiges Technologieunternehmen für klinische Studien, das sich auf komplexe Studien in therapeutischen Bereichen wie Onkologie, Zentralnervensystem (ZNS) und seltene Krankheiten spezialisiert hat, gab den Erhalt eines Patents vom US-Patentamt für die Suvoda Questionnaire Definition Language (SQDL) bekannt, die Teil der Softwarearchitektur seines Produkts eCOA (electronic Clinical Outcome Assessment) ist. Das Patent demonstriert die Leistungsfähigkeit von Suvoda eCOA: beschleunigte Erstellung, Übersetzung, Lokalisierung und Bereitstellung von Fragebögen, damit Sponsoren klinischer Studien ihre Studien effizienter durchführen können. Während eCOA traditionell ein Engpass bei der Durchführung klinischer Studien ist, ermöglichen Suvoda eCOA und sein SQDL-Tool den Sponsoren, qualitativ hochwertige Fragebögen in wenigen Stunden statt in Tagen zu liefern

PR Newswire
Nov 14th, 2024
Suvoda Obtient Un Brevet Américain Pour Son Architecture Logicielle Ecoa

L'approche low-code/no-code accélère la conception et le déploiement des questionnaires eCOA, en éliminant du chemin critique la création des questionnaires, les licences et la localisation. PHILADELPHIE, 14 novembre 2024 /PRNewswire/ -- Suvoda, une société mondiale de technologie d'essais cliniques spécialisée dans les études complexes dans des domaines thérapeutiques tels que l'oncologie, le système nerveux central (SNC) et les maladies rares, a annoncé la réception d'un brevet de l'Office américain des brevets pour le Suvoda Questionnaire Definition Language (SQDL), qui fait partie de l'architecture logicielle de son produit eCOA (évaluation électronique des résultats cliniques). Le brevet démontre la puissance de la solution eCOA de Suvoda : accélération de la création, de la traduction, de la localisation et du déploiement des questionnaires afin que les promoteurs d'essais cliniques puissent lancer leurs études plus efficacement. Alors que l'eCOA est traditionnellement un goulot d'étranglement dans la mise en œuvre des essais cliniques, l'eCOA de Suvoda et son outil SQDL permettent aux promoteurs de fournir des questionnaires de haute qualité en quelques heures, au lieu de quelques jours

PR Newswire
Nov 14th, 2024
Suvoda Obtiene Patente De Ee.Uu. Por Su Arquitectura De Software Ecoa

El enfoque de código bajo y sin código acelera el diseño y la implementación del cuestionario eCOA, lo que elimina la creación, la concesión de licencias y la localización del cuestionario de la ruta crítica. PHILADELPHIA, 14 de noviembre de 2024 /PRNewswire/ -- Suvoda una empresa global de tecnología de ensayos clínicos especializada en estudios complejos en áreas terapéuticas como oncología, sistema nervioso central (SNC) y enfermedades raras, anunció la recepción de una patente de la Oficina de Patentes de EE.UU. para el Suvoda Questionnaire Definition Language (SQDL), parte de la arquitectura de software de su producto eCOA (evaluación electrónica de resultados clínicos). La patente demuestra el poder de Suvoda eCOA: creación, traducción, localización e implementación aceleradas de cuestionarios para que los patrocinadores de ensayos clínicos puedan lanzar sus estudios de manera más eficiente. Si bien eCOA es tradicionalmente un cuello de botella en la implementación de ensayos clínicos, Suvoda eCOA y su herramienta SQDL permiten a los patrocinadores entregar cuestionarios de alta calidad en cuestión de horas, en lugar de días

PR Newswire
Jun 26th, 2024
Suvoda Amplía Su Oferta De Ensayos Clínicos Con La Introducción De Epatient

-  Con el objetivo de mejorar la experiencia del paciente y reducir la carga en los sitios. FILADELFIA, 26 de junio de 2024 /PRNewswire/ -- Suvoda LLC, una empresa global de tecnología de ensayos clínicos que se especializa en estudios complejos en áreas terapéuticas como oncología, sistema nervioso central (SNC) y enfermedades raras, ha dado a conocer el lanzamiento pionero de su producto ePatient. Esta solución innovadora está diseñada para abordar las complejidades, ineficiencias y frustraciones a las que se enfrentan los pacientes con los pagos de remuneraciones y reembolsos, así como con la gestión de citas, a lo largo de su proceso de ensayo clínico. ePatient está configurado para transformar la experiencia del paciente al unificar pagos, citas, recordatorios y cuestionarios eCOA en una única interfaz móvil fácil de usar con el diseño simple e intuitivo por el que Suvoda es conocido. La perfecta integración de la aplicación con IRT y eConsent de Suvoda garantiza una experiencia de usuario coherente, lo que permite a los usuarios del sitio y a los pacientes moverse sin esfuerzo entre todos los productos de Suvoda con un inicio de sesión único