Irb Coordinator Jobs

Excellent time management skills and meet deadlines

Working knowledge of Microsoft Suite, SharePoint, Adobe Suite, Clinical Trials Management System.

Previous experience working with online/web-based platforms for clinical trial management systems

Manage the regulatory tracking and archive systems (e.g. SharePoint, Clinical Trials Management System, shared network drive, etc.).

A minimum two years of regulatory, human research protection or related experience in a research environment.

Previous work experience preparing and/or reviewing study start-up documents, including IRB documentation and research protocols.

Time management skills and the flexibility to accommodate changing priorities in unit.

Thorough knowledge and experience with quantitative and qualitative research design; scientific research concepts and terminology

Bachelor's degree in related area and three or more years of relevant expierience and / or equivalent experience / training

Thorough knowledge and ability to apply all relevant Federal, state, and university regulations, policies, and federal guidance documents

Independence, planning and decision-making abilities to complete assigned duties.

Excellent customer service skills, pleasant, helpful, and patient.

Critical thinking skills; Delegation skills

Written and verbal communication skills

Clinical skills appropriate to position

Knowledge of regulatory standards appropriate to position

Computer skills appropriate to position

Interpersonal skills; Customer service skills