Protocol Coordinator; Fully Remote

• Lead the development and drafting of clinical research protocols in collaboration with study chairs and committees.
• Ensure protocols meet regulatory and departmental standards for accuracy and consistency.
• Oversee protocol amendments and final study closure documentation.

Document Coordination and Quality:

• Prepare and maintain study-related documents including informed consent forms and training materials.
• Review case report forms for consistency with approved protocols.
• Facilitate communication between investigators, coordinators, and external research organizations.

Study Planning and Stakeholder

Collaboration:

• Establish development objectives and coordinate weekly study meetings.
• Design experimental study schemas and therapy delivery maps.
• Identify documentation inconsistencies and coordinate necessary amendments to support timely study activation.

Our partner is a collaborative research organization focused on advancing treatments for childhood and adolescent cancer through clinical trials. They are mission-driven and growing, with a small but dedicated team.