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Champions Oncology, Inc.

Study Coordinator, PL

Champions Oncology, Inc.

. Serve as the primary supporting role for the Project Leadership team managing client sponsors’ scientific design, PDX tumor model selection, and project execution .

Posted 9/22/2026full-timeRemote • United StatesMid-LevelSenior💰 $50,000 - $65,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in project management within oncology research, including proficiency in managing in vivo studies and coordinating study protocols. Strong ability to work collaboratively while maintaining attention to detail and effective communication skills.

Highest-signal resume keywords
Project ManagementIn Vivo Oncology ModelsDatabase ManagementEffective CommunicationAttention to Detail

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Project ManagementIn Vivo Oncology ModelsDatabase ManagementStudy Protocol DraftingTimelines ManagementPre-Clinical ResearchScientific DesignStudy SchedulingEnrollment ReviewProblem Resolution
Soft Skills
Collaborative AttitudeInterpersonal SkillsTimely Decision MakingSelf-OrganizationAdaptability
Tools & Technologies
Laboratory Information Management SystemMicrosoft WordMicrosoft Excel
Industry Keywords
Contract ResearchOncology ResearchPDX Tumor ModelStudy Materials ProcurementStudy Information Management

About the role

Key responsibilities & impact
  • Serve as the primary supporting role for the Project Leadership team managing client sponsors’ scientific design, PDX tumor model selection, and project execution
  • Enter study information into databases for project management
  • Assist in generating estimated study timelines
  • Plan and schedule studies with project leadership and operations teams
  • Update study information to capture protocol amendments
  • Manage and update project timelines and milestones in databases
  • Coordinate procurement of study materials with operations
  • Create initial study protocol drafts and amendments
  • Manage ongoing studies in the laboratory information management system with the Project Leader
  • Perform and/or review enrollment of in vivo studies
  • Assist in scheduling end-of-study activities and analyses
  • Arrange shipment of samples to collaborators, clients, and laboratories
  • Identify and help resolve problems involving ongoing studies
  • Participate in team meetings and provide feedback
  • Work independently and perform other related duties as assigned

Requirements

What you’ll need
  • B.S. degree with appropriate experience or M.S. degree with a focus on a biology or chemistry related field; oncology a plus
  • 1 to 3 years of experience in contract research, pre-clinical research or a similar position is preferred but not required
  • Knowledge of project management and oncology research
  • Knowledge of in vivo oncology models (Xenograft/PDX) preferred
  • Ability to work in multiple databases to assist in project management
  • Collaborative, can-do attitude
  • Timely decision making, good interpersonal skills and ability to be persistent while maintaining tact
  • Ability to balance several priorities simultaneously with high attention to detail
  • Ability for frequent adaptation, self-organization, and accountability
  • Effective oral and written communication skills
  • Proficiency in Microsoft Word and Excel
  • Must be able to sit for long periods using a computer in a typical office environment or home office