Clinical Research Administrator II — Hybrid Eligible

UAB Medicine

University (FL)

Hybrid

USD 48,000 - 77,000

Full time

14 days+

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Job summary

University of Alabama at Birmingham (UAB) hosts the O’Neal Comprehensive Cancer Center, seeking a Clinical Research Administrator II to support the Protocol Review Monitoring System. You will navigate contract principles, federal regulations, and UAB policies in clinical research activities.

The role involves liaising with Offices of Industry Engagement and Sponsored Programs, identifying risks, and maintaining GCP familiarity; you will help coordinate studies, prepare agendas, and document

Qualifications

  • Bachelor's degree in a related field and three (3) years of related experience required.
  • Work experience may substitute for education requirement.
  • Knowledge of clinical trial processes.
  • Data collection and data entry skills.
  • Knowledge of protocols and standard operating procedures (SOPs) for data quality assurance.

Responsibilities

  • Liaise between O'Neal CCC UAB Offices of Industry Engagement and Sponsored Programs in negotiating confidentiality agreements (CDAs), contracts, and amendments related to the conduct of clinical research activities.
  • Identify conflicts of interest, legal, IP and business/financial risk.
  • Maintain familiarity with Good Clinical Practice (GCP) guidelines and regulations.
  • Assist in meeting facilitation by scheduling meetings, creating agendas, distributing materials, and recording minutes.
  • Assist in managing other working groups and studies; arrange trainings and meetings; help formulate operating goals for the research program.

Education

Bachelor's degree in a related field

Job description

University of Alabama at Birmingham (UAB) hosts the O’Neal Comprehensive Cancer Center, seeking a Clinical Research Administrator II to support the Protocol Review Monitoring System. You will navigate contract principles, federal regulations, and UAB policies in clinical research activities.

The role involves liaising with Offices of Industry Engagement and Sponsored Programs, identifying risks, and maintaining GCP familiarity; you will help coordinate studies, prepare agendas, and document

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