The Global Study Coordinator (internal title) is a part-time contract role (up to ~25 hrs/week, hourly, remote - UK) supporting Global Study Managers in planning and operations of active clinical trials. Serves as main point of contact for patient communications and manages all participant travel and logistics, travel budgets, vendor and clinical-site coordination, database setup/transfer, and report preparation. Requires fluent English and Spanish and working knowledge of Microsoft Office; 2+ years' experience in travel and/or pharma preferred.

Associate Project Manager II responsible for designing IRT solutions, liaising with clients, documenting requirements, managing project schedules and scope, supporting UAT, and providing training and post-go-live support for clinical trial systems. Requires a bachelor's degree (life sciences or computer science preferred) and at least 2 years of relevant experience.

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.

Suvoda seeks a Software Developer to join cross-functional teams building Interactive Response Technology (IRT) for randomization and drug supply management in clinical trials. Responsibilities include implementing C#/.NET web applications (MVC, Entity Framework, SQL Server), creating technical and implementation designs, managing deployments, assisting support with production issues, and contributing ideas for product improvements. The role requires at least 2 years' experience and is based in Bucharest, Iasi, or remote within Romania.

Join Suvoda as a Senior Automation Test Engineer focused on ensuring clinical trial software quality and patient-safety critical data integrity. Responsibilities include reviewing requirements, developing validation and risk-based test plans, authoring and automating test scripts (Java/Selenium), API and web testing, setting up test environments, defect tracking, and assisting deployments and support. Minimum 4 years' automation testing experience and strong English communication required.

Responsible for coordinating communication between Suvoda eCOA teams, instrument license holders, and translation vendors; researching licensing and eCOA requirements; preparing and proofreading screen reports and .json files; and managing related timelines. Requires a bachelor's degree and 2+ years' experience in the pharmaceutical industry, strong licensing experience, and project management skills.

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.

Contract, part-time (up to ~25 hrs/week) Global Study Coordinator supporting Global Study Managers in planning and operations of active clinical trials. Acts as main contact for patient communications and coordinates air, hotel, ground accommodations, travel budgets, vendor interactions, data maintenance, and reporting. Requires fluent Spanish and English, ~2+ years preferred in travel and/or pharma, and ability to work remotely from a home office.

Provide implementation and ongoing maintenance of Interactive Response Technology (IRT) systems for clinical trials, including change control, data integration specifications, support escalation, creation of training materials and study documentation, support reporting, and identification of recurring support issues. Requires at least 2 years of related experience and a bachelor’s degree.