Suvoda
501 - 1000 employees
🏥 Healthcare
📦 Logistics
💼 Consulting
💰 $40M Venture Round on 2019-12
Healthcare • Logistics • Consulting
Suvoda is a company specializing in delivering cutting-edge software solutions for managing complex clinical trials. It offers a single platform with products such as eConsent, Interactive Response Technology (IRT), electronic Clinical Outcome Assessment (eCOA), and ePatient, designed to streamline and enhance the efficiency of life-sustaining clinical studies, especially those in therapeutic areas like oncology and rare diseases. With their technology, they aim to provide full command over time-sensitive patient interactions and assist clinical trials in handling infinite variables and constant changes, ensuring high standards and effective patient consent management across various age groups to improve trial outcomes. Suvoda emphasizes collaboration with clients throughout the lifespan of a trial to maintain quality and success.
Implementation Specialist
🔥 0 minutes ago
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Suvoda
501 - 1000 employees
🏥 Healthcare
📦 Logistics
💼 Consulting
💰 $40M Venture Round on 2019-12
Healthcare • Logistics • Consulting
Suvoda is a company specializing in delivering cutting-edge software solutions for managing complex clinical trials. It offers a single platform with products such as eConsent, Interactive Response Technology (IRT), electronic Clinical Outcome Assessment (eCOA), and ePatient, designed to streamline and enhance the efficiency of life-sustaining clinical studies, especially those in therapeutic areas like oncology and rare diseases. With their technology, they aim to provide full command over time-sensitive patient interactions and assist clinical trials in handling infinite variables and constant changes, ensuring high standards and effective patient consent management across various age groups to improve trial outcomes. Suvoda emphasizes collaboration with clients throughout the lifespan of a trial to maintain quality and success.
📋 Description
• Review and interpret global client documentation of payable activities, including contracts, budgets, and amendments • Identify quality risks and needs to support a best-in-class client, site, and patient experience • Extract and configure client data into payable activities from source documents • Collaborate with business partners to verify interpretations of payable activities • Follow auditing and monitoring checklists and procedures • Meet internal KPIs and client-driven SLAs • Participate in internal and external study implementation calls and resolve complex configuration issues • Consult with clients and Client Delivery colleagues to achieve resolution and follow best practices • Contribute to internal process documents for consistent, best-practice study configurations • Partner with Product and IT teams to identify platform enhancements • Support Client Delivery in establishing and maintaining positive client relationships • Perform other duties, assignments, and special projects as needed
🎯 Requirements
• Minimum of 1–3 years in the pharmaceutical or CRO industry, with contract management-related experience preferred • Ability to dissect key elements of clinical trial financial documents and identify payable activities • Ability to handle high volume in a fast-paced environment • Excellent writing skills • Quality and risk-mitigation mindset required • Excellent analytical, organizational, communication, and interpersonal skills • Exceptional time-management skills to support shifting priorities and key client deliverables • Strong attention to detail required • Experience with Microsoft Word and Excel required
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