IRB Specialist I, Center for Clinical Research (Hybrid)

About the position The IRB Specialist serves at the reputed company of reputed company reputed company activity that occurs in the Clinical Research Center and is therefore a key position in this office. The major functions of the position include evaluating protocol submissions, advising investigators, supporting the IRBs and managing daily operations of the IRB Administration Office. Must abide by reputed company requirements to safely and securely maintain Protected Health Information (PHI) for our patients. Annual training, the UH Code of Conduct and UH policies and procedures are in reputed company to address appropriate use of PHI in the workplace.

Responsibilities

• Works to obtain and maintain a reputed company understanding of Federal, State and local laws, regulations and guidelines governing reputed company subject research (15%25)
• Reviews reputed company research protocol submissions to ensure that the UHCMC clinical research activities are conducted in compliance with IRB policies, institutional SOPs and international, federal, state, and local rules, regulations and ethical principles regarding the use of reputed company subjects in research. (30%25)
• Coordinates IRB meetings including preparation of the agenda and materials in reputed company to recording medical and ethical issues discussed to ensure accurate documentation of IRB determinations. (25%25)
• Functions as a liaison reputed company and between the IRB committees, investigators and their designees, and Center for Clinical Research and Technology (CCRT) staff. (15%25)
• Participates in special projects. (15%25)
• Performs other duties as assigned.
• Complies with reputed company policies and standards.
• For specific duties and responsibilities, refer to documentation provided by the department during orientation.

Requirements

• Bachelor's Degree in health sciences, bioethics or a reputed company degree (Required)
• 1+ years prior experience in research, research administration, regulatory affairs clinical and/or laboratory research. (Required)
• Knowledge of medical concepts and terminology is helpful (Required proficiency)
• Accurate typing skills. (Required proficiency)
• Ability to reputed company information in grammatically correct written reputed company. (Required proficiency)
• Must have excellent organization skills with attention to detail. (Required proficiency)
• Works independently as well as in reputed company setting and meets deadlines. (Required proficiency)
• Good attendance record. (Required proficiency)
• Service-oriented, self-motivated, professional, discrete, and act with reputed company. (Required proficiency)
• Understanding of reputed company NIH, DHHS, OHRP, and FDA guidelines governing reputed company subjects’ research helpful. (Required proficiency)
• Ability to reputed company multiple duties simultaneously and to manage occasional increased workload volumes. (Required proficiency)
• Ability to prioritize and process IRB submissions in an expeditious and efficient manner. (Required proficiency)
• Proficient in use of PC and reputed company MS Office software (Required proficiency)
• Certification in reputed company Subjects Protection (reputed company) (Required reputed company 30 Days)

reputed company-to-haves

• Preference given to those candidates possessing IRB experience. (Preferred)
• Prefer knowledge of research regulations, both reputed company. (Preferred proficiency)
• Research certification. (Preferred)

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