IRB Specialist II Research Institute Review

All the benefits and perks you need for you and your family:

• Benefits from Day One
• Paid Days Off from Day One
• Student Loan Repayment Program
• Career Development
• Whole Person Wellbeing Resources
• Mental Health Resources and Support
• Pet Insurance*
• Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)

Our promise to you:

Joining AdventHealth is about being part of something bigger. It's about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.

Schedule: Full-Time/Day

Shift : Monday-Friday 8:00am-5:00pm

Location: 800 N Magnolia Ave, Suite 500, Orlando, FL 32803

The role you'll contribute:

The IRB Specialist II is knowledgeable in the areas of state and federal laws and regulations, ethical issues, institutional policies, and other agency requirements which govern the protection of human subjects in research. The IRB Specialist II conducts quality control functions for the IRB office that may extend to all areas of the operation including review of files and meeting minutes for completeness, accuracy and consistency. The IRB Specialist II provides training for IRB Office Coordinators, external IRB review processes, and the IRB electronic submission process. Actively participates in outstanding customer service and accepts responsibility for maintaining relationships that are equally respectful to all.

The value you'll bring to the team:

• Reads and interprets current regulations, guidelines, and trends influencing the conduct of human subject research.
• Interacts with management and staff to provide useful information, guidance, and integrity to human subject research activities
• Assist in development of, update, and communicate policies and procedures in research administration.
• Monitor, review, and report on performance measures. Audit and monitor studies and consent process.
• Conducts educational classes' specific to human subject research to both researchers and IRB members.
• Counsels investigators and support staff in resolving IRB committee contingencies.

Qualifications
The expertise and experiences you'll need to succeed:

• Bachelor's degree in legal studies, healthcare, business administration, finance, accounting, or research-related field, AND three (3) years of IRB or research related experience preferably in an academic or medical setting; OR
• Associates degree in legal studies, healthcare, business administration, finance, accounting, or research-related field AND five (5) years of IRB or research related experience preferably in an academic or medical setting.
• Certified Institutional Review Board Professional

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