Experience:
1-3 years of experience
Concerned about your lack of experience? Learn More...
Employment Type:
Full time
Posted:
2/19/2018
Job Category:
Research
Industry:
Other
Compensation:
56.00
IRB Administrator - 6 month contract
(This job is no longer available)
Enclipse Corp. | Oakland, CA
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Job Description

IRB Administrator

Description:
Acts as point person for regulatory questions, and for decision-making and problem-solving for day-to-day IRB operations including the resolution of technical problems and questions of IRB support staff, IRB members, and investigators.

Top Daily Responsibilities:

  • Identify issues or concerns that must be addressed in order to approve the research under the expedited procedure.

  • Acts as point person for scientific questions, and for decision-making and problem-solving for day-to-day IRB operations including the resolution of technical problems and questions of IRB support staff, IRB members, researchers and investigators.

  • Communicates with investigators to facilitate the review process while incorporating complex scientific and regulatory language and concepts

Requirements:

  • Experience and/or the ability to be a member of the IRB Committee and/or an Expedited reviewer for biomedical and/or behavioral research.

  • Has the ability to investigate, comprehend, and interpret applicable internal, federal, and state policies and procedures, and communicate these to stakeholders

  • Demonstrated strong interpersonal, oral and written communication skills.

  • Has the ability to supervise, advise and counsel on matters of general research compliance and ethical human participant research practices.

  • Ability to independently manage several projects at once and ability to work in a high volume fast passed work environment. Must be organized and re-prioritize tasks as needed, and be flexible.

  • Has a working knowledge of scientific and medical concepts and terminology

  • Bachelor's degree strongly preferred, High school diploma required

  • Minimum four (4) years in clinical research or clinical trials, clinical research compliance, the protection of human subjects, or equivalent with Bachelor's degree, 6 years if HS only.

  • Minimum four (4) years of experience with federal, state, and local regulations related to protection of human subjects and applying ethical principles regarding protection of human subjects

This person is required to work onsite 100%

Qualifications

Applicants must be eligible to work in the specified location