Suvoda

About Suvoda

Streamlining clinical trials with advanced IRT solutions

🏢 Tech👥 251-1K📅 Founded 2012📍 Conshohocken, Pennsylvania, United States

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...

Suvoda

Global Study Coordinator Entry-Level

SuvodaUnited States - Remote

Posted 2w ago🏠 RemoteEntry-Level📍 United States💰 $25 - $25 / hourly
Apply Now →

Overview

Suvoda is hiring a Global Study Coordinator to support the planning and operations of clinical trial studies. You'll manage patient communications and logistical details while working in a diverse team. This is a part-time contract position based in the United States.

Job Description

Who you are

You are driven to achieve goals and looking to make a direct impact in a collaborative environment. You thrive in a culture where communication across departments is valued and where you can contribute innovative ideas to improve processes. You are eager to grow your career and take on responsibilities that support the success of clinical trials.

What you'll do

As a Global Study Coordinator, you will be responsible for supporting the team of Global Study Managers in the planning and operations of active clinical trial studies. You will act as the main point of contact for patient communications, managing all travel and logistical details for trial participants. Your role will involve managing the travel and transportation budget, participating in discussions with vendors, and supporting hospital staff with trial participant enrollments and visit schedules. You will also maintain accurate data by setting up databases and transferring information between internal systems, ensuring that all inquiries from trial participants and clinical staff are addressed promptly.

What we offer

This position is part-time, potentially up to 25 hours per week, and pays on an hourly basis. While hours are not guaranteed, you will have the opportunity to work in a supportive environment that values diversity and innovation. You will be part of a team that is dedicated to making a positive impact in the field of clinical trials.

Interested in this role?

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