Technical Consultant
Required skills
- Technical Consultant
- randomization
- drug supply management
- eClinical solutions
- data integration
- data review plans
- system change controls
- customer care
- troubleshoot
- process improvements
Role summary
Suvoda is seeking a Technical Consultant with at least 3 years of experience to manage the delivery and maintenance of Interactive Response Technology (IRT) systems for clinical trials. Responsibilities include overseeing IRT systems, managing change controls, designing data integrations, creating data review plans, developing training materials, and troubleshooting escalated support issues. The role requires strong analytical, communication, and problem-solving skills, with a deep understanding of the clinical trial industry and Suvoda's software products. Travel to client sites for meetings and training is expected.
Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease.
Supporting clinical trials means supporting unique experiments that are inherently complex, high-stakes, and dynamic. It is imperative that Suvoda staff working with clients, end-users, or the systems that client and end-users interact with understand the clinical trial industry, regulations, Suvoda’s software products and processes, and especially the specificities of the unique trial in question before taking any actions they may alter the data of the system in question.
Responsibilities:
Requirements:
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