
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...

Project Manager β’ Entry-Level
Suvoda β’ BucureΕti
Overview
Suvoda is seeking an Associate Project Manager II to join their team. You'll work on delivering Interactive Response Technology for clinical trials and support cross-functional project teams. This entry-level role is ideal for candidates who are resourceful problem solvers.
Job Description
Who you are
You are an entry-level, analytically-oriented Associate Project Manager who thrives in a collaborative environment. You take initiative to seek out information and development, demonstrating resourcefulness in problem-solving. You are comfortable with technology and adept at finding effective solutions to complex client challenges. You excel in managing uncertainty and ambiguity, and you prioritize the success of your team above all else.
What you'll do
In this role, you will work as part of a cross-functional project team responsible for delivering Interactive Response Technology (IRT) for randomization and drug supply management in clinical trials. You will liaise with clients to discuss requirements, handle issues, provide status updates, and answer questions. You will design IRT solutions that meet study requirements based on clinical protocols and client discussions. Your responsibilities will include accurately documenting all requirements and participating in internal and external specification review meetings. You will assist with client review meetings of IRT specifications and support documents, making necessary updates. Additionally, you will manage project schedules and scope, tracking all internal and client tasks required to meet project milestones. You will also assist in creating the User Acceptance Testing (UAT) plan and developing test cases to ensure project success.
What we offer
Suvoda provides a supportive environment where you can grow your skills and contribute to meaningful projects in the clinical trial space. You will have the opportunity to work with a talented team and gain valuable experience in project management. We encourage you to apply even if your experience doesn't match every requirement, as we value diverse perspectives and backgrounds.
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