Full-Time

Researcher 2

Ohio State University

Ohio State University

No salary listed

Company Does Not Provide H1B Sponsorship

Columbus, OH, USA

In Person

Category
Lab & Research (2)
,
Required Skills
Ruby
Requirements
  • Master’s Degree or equivalent experience; 3 years of relevant experience required with a Bachelor’s Degree, or 1 year of relevant experience required with a Master’s Degree.
Responsibilities
  • Manage daily ION operations in accordance with NCI/NCTN best practices, including SOP development, biospecimen procurement, banking, characterization, and clinical annotation. Optimize workflows and ensure quality and compliance with institutional, state, and federal regulations (IRB, IBC, HIPAA, biosafety).
  • Coordinate ION activities with the OSUCCC Clinical Trials Office, Biospecimen Shared Resource (TCC), and Clinical Trial Processing Laboratory (CTPL) to ensure seamless sample processing and data integration.
  • Maintain and improve the ION sample inventory database and biorepository systems, ensuring accurate “cradle-to-grave” tracking, chain-of-custody, and environmental monitoring.
  • Assist the IMDP Director with budgeting, financial tracking, annual reports, and grant proposal preparation.
  • Serve as liaison to internal and external investigators, ensuring effective communication, timely response to specimen requests, and adherence to established policies and MTAs.
  • Support onboarding of new PIIO faculty, staff, and trainees; manage guest accounts, lab relocations, and introductions to OSU compliance programs (IBC, IACUC, EHS).
  • Oversee shared equipment operations, including installation, warranty tracking, preventive maintenance, and service contract management.
  • Assist with grant and meeting preparation, including facility documentation, agendas, and materials for donor and partner visits.
  • Contribute to operational planning and implementation to support PIIO research space efficiency, safety, and collaboration.
Desired Qualifications
  • 3+ years of experience in academic or clinical research operations, biobanking, or shared-resource/core facilities.
  • Supervisory experience (technicians or student staff) and basic HR process familiarity within a large institution.
  • Experience coordinating with clinical trials units, biospecimen cores, or processing laboratories.
  • Experience with quality systems (SOPs, CAP/CLIA exposure, audit readiness) and continuous process improvement.
  • Working knowledge of material transfer agreements and data/specimen governance policies.
Ohio State University

Ohio State University

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