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 IRB Coordinator -- Great Neck, NY
Author: Raffaella Hart, CIP
Date:   11-25-09 00:03

The coordinator is responsible for:

· Implementing established procedures to process research study application packets

· Providing support to investigators and research coordinators

· Supervising clerical assistance supporting the administrative review and processing of applications to the IRB

· Maintaining official records of the committee’s activities and preparation of meeting materials assuring that applications are complete and accurate prior to committee review

· Serving as liaison between investigators and IRB to obtain the most expeditious, accurate and complete responses to committee questions

· Coordinating IRB meetings

· Attending IRB meetings to provide technical information pertaining to local, state, and federal regulations governing research

· Overseeing preparation of meeting agendas and minutes

· Participating in training programs for IRB members

· Performing quality assurance reviews for compliance with OHRP/FDA regulations, accreditation standards and internal SOPs

· Maintaining and continually refining customized, networked computerized database to allow for timely tracking of research project submissions

· Drafting appropriate correspondence to investigators

Minimum Requirements:

· Demonstrated written and oral communications skills.

· Ability to perform multiple tasks with a high level of accuracy and attention to detail.

· Working knowledge of research and medical terminology.

· Demonstrated ability to work independently in a team-oriented environment and independently perform against deadlines with competing priorities.

· Ability to exercise sound judgment and initiative in collecting technical information from a wide variety of sources, to maintain confidentiality with tact and discretion, and to interpret and apply ethical principles

· Education and experience equivalent to a Bachelor’s degree in biomedical sciences, ethics, public health or related field

· IRB experience and knowledge of OHRP and FDA regulations is a preferred

Please email your CV/resume and cover letter to Raffaella Hart, BRANY IRB Director at rhart@brany.com.

 Topics Author  Date
 IRB Coordinator -- Great Neck, NY new 
Raffaella Hart, CIP   11-25-09 00:03 


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