Lead product strategy and roadmap for Suvoda's Greenphire Clinical Finance suite with primary focus on Budgeting & Benchmarking and Site Payments. Leverage sponsor-side clinical-finance experience to define initiatives, manage and develop Product Owners, and partner with cross-functional teams to deliver SaaS solutions; typically requires 8+ years of relevant experience.

Product leader with sponsor-side clinical-finance expertise responsible for product strategy, roadmap, and initiative direction across Budgeting & Benchmarking and Site Payments. Manages and develops Product Owners, leads discovery and delivery activities, partners with cross-functional teams (Engineering, UX, Services, Commercial, etc.), and supports implementations, launches, and customer engagements. Typically requires 8+ years of relevant experience implementing clinical-trial finance or related technology.

Suvoda seeks a Sales Compensation Specialist to manage end-to-end monthly/quarterly payout cycles, calculate commissions/variable bonuses, design reporting (attainment, OTE/CTE, run-rate), implement plan changes in ICM/SPM, write basic data queries for analysis/validation, and lead reconciliation and root-cause analysis. Requires 2 years of relevant experience, Salesforce Spiff experience, advanced Excel, intermediate Power BI, and a bachelor’s degree.

Remote (Romania) role to support monthly invoicing and billing calendar, validate billing data against agreements and purchase orders, perform reconciliations and variance analysis using NetSuite and other systems, assist collections and ensure SOX/compliance and accurate process documentation. Requires 1+ years in corporate finance focused on revenue accounting for a SaaS company.

Suvoda seeks an entry-level, analytically oriented Associate Project Manager to work on cross-functional teams delivering IRT solutions for randomization and drug supply management in clinical trials. Responsibilities include client liaison, requirements documentation and specification reviews, project schedule and scope management, UAT planning and support, training delivery, and post‑go‑live client support. A bachelor's degree is required; strong communication, organizational, analytical, and problem‑solving skills are emphasized.

Join Suvoda as a Software Test Engineer II to verify web-based clinical trial software, author and execute test scripts, develop risk-based validation plans, document and track defects, and potentially serve as Lead Project Tester coordinating testing activities. Requires at least 3 years' relevant experience; eClinical domain knowledge and technical skills such as SQL and automation are preferred.

Suvoda seeks a Pricing & Contracts Analyst to calculate financial components of proposals and change orders, manage the change order queue, input study specifications into budget calculators, and coordinate with Finance, Legal, and Project teams. Requires a bachelor's degree and at least 3 years' experience in a similar pricing/contracts role; strong Excel/Word skills and familiarity with CRM/Salesforce are expected.

Suvoda is hiring a Pricing/Contract Analyst to calculate financial components of proposals and change orders, manage the change order queue, and partner with Finance, Legal and Project teams. Requires a Bachelor’s in Finance/Business (or related), at least 3 years of relevant pricing/contract experience, strong Excel and Word skills, familiarity with CRM/Salesforce, and ability to partially overlap with US EST/EDT business hours. Role is based in Romania (Bucharest or Iasi) or remote within Romania.

Suvoda seeks a Software Developer II to work on Interactive Response Technology (IRT) for randomization and drug supply management. Responsibilities include implementing web applications with C#, .NET (Framework or Core), SQL Server, MVC and Entity Framework, producing technical and implementation design documentation, deploying systems, and supporting production issues. Candidates should have at least 2 years of relevant experience; a bachelor’s degree is preferred.

Contract, part-time (up to ~25 hrs/week) Global Study Coordinator based in France responsible for supporting Global Study Managers with planning and operations of active clinical trial studies, serving as main point of contact for patient communications and managing travel/transportation logistics and budgets. Requires fluent French and English, familiarity with Microsoft Office, and ~2+ years' experience in travel and/or pharma preferred.

The Implementation Specialist reviews and interprets clinical study documentation (contracts, budgets, amendments, ICFs, templates) to extract data and create accurate system configurations supporting payments and study activities. The role collaborates with business partners, adheres to auditing/monitoring procedures, meets internal KPIs and customer SLAs, contributes to process documentation, and partners with Product/IT. Requires at least 1 year of pharmaceutical/CRO experience (contract management preferred) and strong Excel/Word, analytical, and communication skills.

Design, develop, test and support clinical trial software with emphasis on patient safety and data integrity. Responsibilities include reviewing requirements, creating technical design and implementation documentation, coding, unit testing, managing deployments, and assisting with production issue resolution. Requires bachelor's degree or equivalent and strong problem-solving, organizational and communication skills; over 5 years of experience.

Responsible for developing project plans (scope, milestones, schedules, resources), tracking progress and changes, coordinating with development and QA, reporting status to stakeholders, identifying and mitigating risks to software releases, and maintaining project documentation. Requires a bachelor’s degree or equivalent, strong communication and organizational skills, and over 3 years managing software development projects.

Work on cross-functional teams to develop Interactive Response Technology (IRT) for randomization and drug supply management. Responsibilities include reviewing requirements, producing implementation and technical design, developing reliable web applications with C#/.NET and SQL Server, managing deployments, supporting production troubleshooting, and contributing to R&D. Minimum 2 years' relevant experience; Bachelor's degree preferred.

Suvoda is hiring a Senior Full-Stack Software Engineer to own features end-to-end for a reporting web application. Responsibilities include building Python backend services (REST APIs, auth/SSO, audit logging, scheduling/background jobs, database schema and migrations), developing React/TypeScript frontend features (dashboards, data grids, permission-aware UI), integrating and maintaining AI-powered features and LLM integrations, containerizing and deploying services (Docker, Kubernetes/Helm), provisioning infrastructure as code (Terraform), and maintaining CI/CD pipelines (GitHub Actions). Requires a technical bachelor's degree and at least 7 years of full-stack experience, strong proficiency in Python and React/TypeScript, SQL and ORM experience, and familiarity with CI/CD, containerization, and infrastructure-as-code.

Contract (part-time, up to 25 hours/week) Global Study Coordinator role supporting Global Study Managers in planning and operations of clinical trials. Main responsibilities include managing patient travel and logistics, acting as primary patient contact, coordinating with vendors and clinical staff, maintaining databases and producing reports. Fluent Hungarian, English and French are required; work is performed from a home office.

Contract, part-time (up to 25 hours/week) remote role based in Hungary. The Global Study Coordinator supports Global Study Managers in planning and operations of active clinical trials, acting as main contact for patient communications and managing patient travel (air, hotel, ground), budgets, vendor interactions, data entry/transfer and reporting. Requires fluent Hungarian, English and French; bachelor's degree or equivalent; Microsoft Office proficiency.

Join a cross-functional team to build Interactive Response Technology (IRT) for randomization and drug supply management. Responsibilities include reviewing requirements, producing technical and implementation design documentation, developing reliable web applications (C#, .NET, MVC, EF, SQL Server), managing deployments, assisting production support, and contributing engineering input to product R&D. Minimum one year of relevant experience is required.

Lead the full sales cycle from opportunity identification through proposal, negotiation, and close; manage RFP/RFI responses; develop and maintain client relationships and account governance; represent the company at industry events and mentor Business Development Associates. Requires a bachelor's degree and at least 7 years of sales experience in the eClinical software field.

The Account Executive will manage the sales process from opportunity identification through proposal, negotiation and close; respond to RFPs/RFIs; develop and maintain client relationships; lead client meetings and governance with strategic accounts; generate leads and collect competitive intelligence. Requires a bachelor's degree and at least 3 years of sales experience in the eClinical software field.