Streamlining clinical trials with advanced IRT solutions
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 ...
Suvoda offers competitive salaries, equity options, generous PTO, and a flexible remote work policy to support work-life balance....
Suvoda fosters a culture centered around innovation in clinical trial technology, emphasizing collaboration and adaptability to meet client needs in a...
Suvoda • Jerusalem, Israel
Suvoda is seeking a Global Study Coordinator to support clinical trial operations and manage patient communications. This part-time role is based in Bucharest and requires strong organizational skills.
You are driven to achieve goals and eager to make a direct impact in a collaborative environment. You thrive in a diverse team setting and communicate effectively across departments. Your innovative mindset allows you to bring efficiencies to processes, and you are looking to grow your career in the clinical research field. You understand the importance of patient communication and logistical management in clinical trials, making you a suitable candidate for this role.
As a Global Study Coordinator, you will support the team of Global Study Managers in planning and executing active clinical trial studies. You will be the main point of contact for patient communications, ensuring that all inquiries are addressed promptly. Your responsibilities will include managing the travel and transportation budget for trial participants, participating in discussions with vendors, and supporting hospital staff with trial participant enrollments and visit schedules. You will also contribute to maintaining accurate data by setting up databases and transferring information between internal systems, as well as aiding in the production of reports related to the trials.
This is a contractor position that offers part-time hours, potentially up to 20 hours per week, with pay on an hourly basis. While hours are not guaranteed, you will have the opportunity to work in a supportive environment that values your contributions to clinical research. You will gain valuable experience in the field and have the chance to grow your skills while making a meaningful impact on patient care.
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