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.

We're looking for a Software Test Engineer to join our team! If you have an interest in technology, an analytical mindset and are motivated by processes and details, then this may be the job for you. Read more about the position below, and consider applying if the description sounds like you!

You Are

• Someone who thrives in a fast-paced, dynamic environment
• A team player who puts the success of the team first
• A go-getter who seeks out information, knowledge and development proactively
• A fast learner that leverages core talents and skills rapidly in new and complex environments
• An analytical thinker who is energized by delving into complex projects
• A resourceful problem-solver who seeks out effective and efficient solutions
• An achiever who always seeks to raise the bar higher
• A true self-starter who deals well with uncertainty and ambiguity
• Savvy with technology

Basic Responsibilities Include (but Are Not Limited To)

• Work as part of a cross-functional project team to deliver custom software solutions that streamline the clinical trial process for pharmaceutical and biotech clients
• Ensure the correct functioning of clinical trial software with focus on patient safety and integrity of clinical study data
• Ensure all activities and deliverables comply with FDA regulations
• Verify that system requirements are clear, testable, and consistent with the clinical trial protocol
• Develop validation plans according to a risk-based testing methodology
• Author and manage the completion of all validation related deliverables on each project
• Author and execute test scripts
• Document defects and track resolution
• Perform other related duties as required

Requirements

• Bachelor's degree (in computer science or another analytical domain preferred)
• 0 to 1 years of experience in IRT or related field preferred
• High achieving, exploratory nature
• Attention to detail
• Analytical reasoning skills
• Desire to learn and grow
• Strong work ethic
• Sense of ownership and proactivity
• Effective prioritization and time management
• Follow through
• Interpersonal and Communication skills
• Technical Knowledge preferred (SQL, programming, automation)

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