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University of KentuckyPosted 24 days ago

Research Regulatory Specialist I

Full-time
Hybrid
1+ years
Competitive
Posted 24 days ago

Responsibilities Duties will include completion of IRB applications with UK and other cancer centers, amendments and renewals, management of all regulatory documentation, responsible conduct of research and human subjects, assure that all center researchers maintain IRB and HIPAA training requirements compose and conduct safety review meetings as needed Incumbent will also maintain organization database listing for a

Posted
24 days ago
Source
ukjobs.uky.edu
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • Duties will include completion of IRB applications with UK and other cancer centers, amendments and renewals, management of all regulatory documentation, responsible conduct of research and human subjects, assure that all center researchers maintain IRB and HIPAA training requirements compose and conduct safety review meetings as needed
  • Incumbent will also maintain organization database listing for all center projects, including periodic project renewals, and will manage organizational filing of regulatory documents for center research projects
  • Coordinates and performs a variety of research and administrative activities required in the management of clinical trials research
  • Duties include coordinating the preparation and submission of reports, documents, and correspondence for regulatory agencies and internal review board; interpreting and applying regulatory and policy requirements to protocols

Qualifications

  • Bachelors degree and at least one year of related experience or UK equivalencies

Required skills

Bachelor's DegreeBachelor’s Degree

Nice to have

BA4years/1year

Full job description

Responsibilities

  • Duties will include completion of IRB applications with UK and other cancer centers, amendments and renewals, management of all regulatory documentation, responsible conduct of research and human subjects, assure that all center researchers maintain IRB and HIPAA training requirements compose and conduct safety review meetings as needed
  • Incumbent will also maintain organization database listing for all center projects, including periodic project renewals, and will manage organizational filing of regulatory documents for center research projects
  • Coordinates and performs a variety of research and administrative activities required in the management of clinical trials research
  • Duties include coordinating the preparation and submission of reports, documents, and correspondence for regulatory agencies and internal review board; interpreting and applying regulatory and policy requirements to protocols

Preferred

  • BA4years/1year

Benefits

  • This position will have a hybrid work arrangement after the initial training.
  • Glassdoor
  • 3.9
  • The University of Kentucky is a public, research-extensive, land grant university dedicated to improving people's lives through excellence in teaching, research, health care, cultural enrichment, and economic development for over 150 years.
  • Lexington, Kentucky, USA
  • https://www.uky.edu
  • Distribution of Different Job Fields Receiving Sponsorship
  • Represents job field similar to this job
  • Legal and Compliance
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  • Engineering and Development
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  • Accounting and Finance
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  • Trends of Total Sponsorships
  • *2026
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  • 2021
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  • Late Stage
  • Leadership Team

Qualifications

  • BS
  • 1 yr
  • Bachelors degree and at least one year of related experience or UK equivalencies
  • BA4years/1year
  • Bachelors degree and at least one year of related experience or UK equivalencies.

Required skills

  • 1 Year's Experience, 4 Years' Experience, Bachelor's Degree, Bachelor’s Degree, Related Experience

Preferred skills

  • BA4years/1year

Experience

  • 1+ years

Job details

Employment type

Full-time

Seniority level

1+ years

Date posted

Oct 20, 2026

Work mode

Hybrid

Job source

ukjobs.uky.edu

Company

University of Kentucky

Healthcare

  • Lexington, KY
  • Healthcare

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Research Regulatory Specialist I

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