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 ...
π Benefits
Suvoda offers competitive salaries, equity options, generous PTO, and a flexible remote work policy to support work-life balance....
π 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 Technical Consultant I to support clinical trials through the delivery of Interactive Response Technology (IRT). You'll work with clients and project teams to ensure successful implementation and maintenance of IRT systems. This position is suitable for entry-level candidates.
Job Description
Who you are
You are an entry-level professional eager to dive into the clinical trial technology space. You have a foundational understanding of the clinical trial industry and are keen to learn about regulations and software products that support this critical field. You possess strong communication skills and are comfortable working with clients and project teams to deliver effective solutions.
You are detail-oriented and understand the importance of maintaining data integrity in high-stakes environments. You are ready to take on responsibilities that involve oversight of IRT systems and are motivated to identify and mitigate potential issues that may arise during project execution.
What you'll do
In this role, you will work closely with assigned clients and project teams to deliver Interactive Response Technology (IRT) solutions for randomization and drug supply management. You will be responsible for the overall maintenance of the teamβs IRT systems, ensuring that support processes are followed and that any potential risks are identified and addressed promptly. You will lead the implementation of system change controls during the maintenance phase of studies, ensuring that all changes are documented and communicated effectively.
You will manage the design of study data integration specifications between the IRT system and other eClinical solutions, creating data review plans to ensure that reviews are completed on time. Your role will require collaboration with various stakeholders, including clients and other vendors, to ensure the success of the IRT system in supporting clinical trials.
What we offer
Suvoda offers a dynamic work environment where you can grow your skills in the clinical trial technology sector. You will have the opportunity to work on meaningful projects that impact patient interactions in life-sustaining studies. We encourage you to apply even if your experience doesn't match every requirement, as we value diverse backgrounds and perspectives in our team.
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