
About Suvoda
Streamlining clinical trials with advanced IRT solutions
Key Highlights
- Headquartered in Conshohocken, PA
- Specializes in SaaS for clinical trial management
- 4-6 week deployment for IRT/IWRS solutions
- Serves numerous biopharmaceutical clients
Suvoda, headquartered in Conshohocken, Pennsylvania, specializes in SaaS solutions for randomization and trial supply management in clinical trials. Their Interactive Response Technology (IRT/IWRS) is utilized by biopharmaceutical companies to streamline processes, boasting a deployment time of 4-6 ...
🎁 Benefits
Suvoda offers competitive salaries, equity options, generous PTO, and a flexible remote work policy to support work-life balance....
🌟 Culture
Suvoda fosters a culture centered around innovation in clinical trial technology, emphasizing collaboration and adaptability to meet client needs in a...
Overview
Suvoda is hiring a Software Test Engineer to ensure the functionality of clinical trial software. You'll focus on patient safety and data integrity while developing validation plans. This role requires an analytical mindset and attention to detail.
Job Description
Who you are
You have a keen interest in technology and possess an analytical mindset that drives your motivation for processes and details. Your understanding of the clinical trial industry and its regulations is crucial, as you will be working with software products that support complex and high-stakes clinical studies. You are detail-oriented and committed to ensuring the integrity of clinical study data, which is vital for patient safety. Your ability to verify that requirements are clear and testable aligns with the expectations of this role, making you a strong candidate for the Software Test Engineer position at Suvoda.
What you'll do
As a Software Test Engineer, you will be responsible for ensuring the correct functioning of clinical trial software, with a primary focus on patient safety and the integrity of clinical study data. You will verify that all requirements are clear, testable, and consistent with the clinical trial protocol, ensuring compliance with Suvoda's processes and procedures. Developing validation plans according to a risk-based testing methodology will be a key part of your responsibilities, as will authoring and managing the completion of all validation-related documentation. Your role will involve collaborating with various teams to ensure that the software meets the necessary standards and supports the unique complexities of clinical trials.
What we offer
At Suvoda, you will be part of a global clinical trial technology company that is shaping digital experiences for clinical trial sponsors and site professionals. We offer a supportive work environment where your contributions will directly impact the success of life-sustaining studies in therapeutic areas such as oncology and rare diseases. You will have the opportunity to work remotely while being part of a dedicated team that values your expertise and insights in the clinical trial domain.
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