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Central Study Coordinator - Remote

Posted 8 weeks ago
Project Management
Full Time
Worldwide

Overview

The Central Study Coordinator (CSC) position combines clinical research and project management skills into a singular role that delivers a strong customer experience for both patients and sites.

In Short

  • Manage study work for each assigned site as delegated by the PI.
  • Build strong rapport with sites, participants, CRAs, and sponsor contacts.
  • Host regular calls with each assigned PI and present on key elements of the study.
  • Facilitate communication between study site, CRA, and sponsor.
  • Perform the Informed Consent process with study participants virtually.
  • Schedule, prepare for, and facilitate participant visits in accordance with the study protocol.
  • Enter data and resolve queries in EDC and other portals.
  • Ensure all study trackers and systems are up to date daily.
  • Support site compliance with subject safety reporting.
  • Additional duties and responsibilities may be assigned as needed.

Requirements

  • At least 3 years of relevant clinical research experience.
  • Proficient with Microsoft Office applications.
  • Strong communication customer service abilities.
  • High attention to detail.
  • Ability to work effectively in a remote environment.
  • Proper home office set-up including a private space for participant communication.

Benefits

  • PTO/vacation days, sick days, holidays.
  • 100% paid medical, dental, and vision Insurance.
  • HSA plan.
  • Short-term disability, long-term disability, and life Insurance.
  • 401k retirement plan.
Care Access logo

Care Access

Care Access is a healthcare organization dedicated to improving patient access to clinical trials and innovative treatments. The company focuses on bridging the gap between patients and cutting-edge medical research, ensuring that individuals have the opportunity to participate in studies that can lead to advancements in healthcare. With a commitment to patient-centered care, Care Access collaborates with various stakeholders in the medical community to enhance the clinical trial experience and promote better health outcomes.

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