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Remote Regulatory Assistant Job at The Ohio State University USA

Regulatory Assistant Role at The Ohio State University USA

The Regulatory Assistant – CCC position is a full-time remote job opportunity within the Clinical Trials Office at The Ohio State University. This regulatory job focuses on supporting clinical research activities by ensuring compliance with university, state, and federal regulations across multiple research groups.

Job Details:

  • Job Role: Regulatory Assistant – CCC
  • Department: Clinical Trials Office (CTO)
  • Location: Remote job (Home Office, Ohio)
  • Employment Type: Full-time
  • Job Number: R144593
  • Career Level: Individual Contributor – Technical – T2 Experienced

About The Ohio State University:

The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute is one of only 50 designated comprehensive cancer centers in the United States. The organization is committed to laboratory, clinical, and population-based cancer research, applying discoveries to improve cancer prevention, diagnosis, and treatment. Its mission reflects the belief that a Cancer-Free World Begins Here. Explore more remote job offers.

Educational Requirements:

  • Bachelor’s degree preferred in biological sciences, health sciences, or life sciences
  • Equivalent combination of education and experience accepted
  • Experience in a clinical research capacity is desirable

Key Responsibilities of the Remote job:

  • Assist with regulatory functions supporting clinical research activity
  • Prepare protocol submissions to Institutional Review Boards (IRBs)
  • Provide updates on IRB submission status
  • Prepare and manage required regulatory documents
  • Distribute approved regulatory documents
  • Relay regulatory information to clinical research staff
  • Perform data entry and document maintenance in the OnCore electronic database
  • Assist with monitoring visits and regulatory issues
  • Create and maintain regulatory files

Skills Required for the Remote job:

  • Knowledge of regulatory compliance in clinical research
  • Familiarity with IRB submission processes
  • Strong documentation and organizational skills
  • Experience with database software applications
  • Basic computer proficiency and data management skills
  • Ability to work independently in a remote job environment

Benefits of the Regulatory Assistant Role:

  • Opportunity to work in a remote job setting
  • Exposure to clinical trials and regulatory operations
  • Career growth within a nationally recognized research institution
  • Contribution to impactful cancer research initiatives
  • Equal opportunity employment environment

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