Full-Time
Suvoda
1,001-5,000 employees
Software solutions for managing clinical trials
No salary listed
Mid, Senior
Remote in USA
- Bachelor’s degree or equivalent experience
- Strong expertise in C#.Net/SQL or JavaScript and its related technologies
- Deep understanding of programming principles
- Ability to design, develop, and support software modules with low to medium complexity
- Excellent problem-solving skills and learning capability
- Excellent time management and organizational skills
- Strong oral and written communication skills
- Demonstrated technical leadership
- Design, develop, and support clinical trial software with emphasis on patient safety and integrity of clinical study data
- Review product requirements and verify that all requirements can be implemented
- Assist with the creation of technical design and implementation documentation
- Design and code software applications and fix defects
- Provide unit testing coverage for delivered code
- Work with others to ensure timely delivery of high-quality code
- Manage software deployment into all environments and complete all required documentation
- Assist support team with troubleshooting and resolution of production issues
- Manage a group of developers
- Oversee and coordinate all development tasks of the group
- Serve as main point of contact for all development-related requests and questions for the group
- Provide continued mentorship and support for group members
- Work with the group to provide task estimates
- Ensure on-time delivery of high-quality work
- Perform other related duties as required
- Over 4 years of experience in .Net or JavaScript software development
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 modular for quick adaptation to various study types, often set up in as little as four weeks. Operating on a software as a service (SaaS) model, Suvoda provides ongoing support and additional services like virtual trial solutions, which are essential for remote patient engagement. The company's goal is to streamline the clinical trial process, enabling faster delivery of new treatments to the market.
Company Size
1,001-5,000
Company Stage
Early VC
Total Funding
$40M
Headquarters
Conshohocken, Pennsylvania
Founded
2012
Simplify's Take
What believers are saying
- The rise of decentralized trials boosts demand for Suvoda's virtual trial solutions.
- AI-driven analytics align with Suvoda's 'Sofia' for optimizing trial management.
- Growing demand for real-world evidence enhances Suvoda's data collection capabilities.
What critics are saying
- Merger with Greenphire may cause integration challenges affecting operations.
- Resistance to AI assistant 'Sofia' could slow its adoption and efficiency gains.
- Pressure to enhance patient-centric features may require additional investment.
What makes Suvoda unique
- Suvoda offers a modular IRT system for rapid clinical trial implementation.
- The company provides virtual trial solutions, crucial during the COVID-19 pandemic.
- Suvoda's AI assistant 'Sofia' simplifies clinical trial management with natural language queries.
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Growth & Insights and Company News
6 month growth
↑ 0%1 year growth
↑ 0%2 year growth
↑ 1%Conshohocken, Pa.-based Suvoda merged with Greenphire, headquartered in King of Prussia, Pa., in March.
CONSHOHOCKEN, Pa. and KING OF PRUSSIA, Pa., April 24, 2025 /PRNewswire/ -- Suvoda, a global clinical trial technology company specializing in randomization and trial supply management, consent, and patient outcomes data collection solutions for complex, life-sustaining studies, and Greenphire, a leader in clinical trial payments, financial management, and patient support tools, today announced the successful completion of their previously announced merger, bringing the two companies under common ownership and management
Suvoda introduces AI assistant 'Sofia' to streamline clinical trial management.
From many clicks to one query, drug supply managers can more quickly access, analyze, and visualize the trial supply data they need.PHILADELPHIA, March 5, 2025 /PRNewswire/ -- Suvoda LLC, a global clinical trial technology company that specializes in complex studies in therapeutic areas like oncology, central nervous system (CNS), and rare disease, today announced the early adopter launch of Sofia, an artificial intelligence assistant designed to simplify how study teams access and review clinical trial information.Sofia is available on the Suvoda Platform and can be enabled by sponsors looking to provide drug supply managers with efficient access to vital information through an intuitive chat interface, reducing what were once multi-screen, multi-click processes to simple conversations."When creating Sofia, we asked ourselves: What if clinical trial staff had an AI assistant that could alleviate their administrative burdens?" said E.K. Koh, Chief Product Officer at Suvoda. "Sofia became our answer. It's an exciting opportunity to streamline the management of clinical trials."Built with Suvoda's commitment to reliability and security, Sofia brings greater efficiency to clinical trial operations, while adhering to data privacy and other regulatory requirements in clinical research.Sofia's key capabilities include:Streamlines Information Retrieval: Users access trial information through natural language queries that simplify navigation. They can now easily find answers that otherwise would span multiple screens, putting information they need at their fingertips.Users access trial information through natural language queries that simplify navigation. They can now easily find answers that otherwise would span multiple screens, putting information they need at their fingertips
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.