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Associate Irb Administrator Jobs in Kentucky (NOW HIRING)

$65 - $90/hr

... IRB and/or FDA submissions (initial, modifications/amendments, continuing reviews, and study ... Administer expedited and exempt research review processes, including, but not limited to: intake of ...

Posted today

$90 - $120/hr

... Compliance, IRB (Human Subject Research Office), Risk Management, sponsors and other relevant ... Assists Assoc. Director/Executive Director, as needed. * Adheres to University and unit‑level ...

New

Our associates are the heart of everything we do. 🌟 Benefits That Support You We invest in you ... Administer investigational study medication and document in the medical record or coordinate the ...

Our associates are the heart of everything we do. 🌟 Benefits That Support You We invest in you ... Administer investigational study medication and document in the medical record or coordinate the ...

Associate Irb Administrator information

What is the difference between Associate Irb Administrator vs Research Coordinator?

AspectAssociate Irb AdministratorResearch Coordinator
CredentialsTypically requires a bachelor's degree, familiarity with IRB processesUsually holds a bachelor's degree, often in health or science fields
Work EnvironmentWorks within IRB offices, focusing on protocol review and complianceWorks directly with research participants and study teams
Employer & IndustryResearch institutions, hospitals, universitiesResearch sites, hospitals, academic institutions
Common Search & ComparisonOften compared for roles supporting IRB functionsCompared for clinical research management roles

The Associate IRB Administrator primarily supports the Institutional Review Board by managing protocol submissions and ensuring compliance. In contrast, a Research Coordinator handles the day-to-day operations of clinical studies, including participant recruitment and data collection. While both roles require knowledge of research regulations, the Associate IRB Administrator focuses more on regulatory oversight, whereas the Research Coordinator is involved in direct research activities.

$65 - $90/hr

Other

Medical, Retirement, PTO

Posted 21 hours ago

Posted today


Job description

WHY UT SOUTHWESTERN?

With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career!


JOB SUMMARY

Works under limited supervision to assure compliance with federal regulations relating to human subject research and/or animal care and use. Understands and applies ethical principles and multiple regulations to complex scientific research projects. The Regulatory Associate will be primarily responsible for regulatory support of a specific Disease Oriented Team's (DOT) clinical trials as well as provide support and backup for other DOTs as needed. The primary role of the regulatory team is to review study protocols, draft consent forms, complete IRB and/or FDA submissions (initial, modifications/amendments, continuing reviews, and study closure), maintenance of essential regulatory documents both electronic and paper, and preparing and facilitating the DOT studies for long term storage at Iron Mountain. In addition, each regulatory team member provides ancillary services such as assisting with and maintaining the CTEP IDs for physicians as well as staff regulatory training.


BENEFITS

UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:



  • PPO medical plan, available day one at no cost for full-time employee-only coverage

  • 100% coverage for preventive healthcare-no copay

  • Paid Time Off, available day one

  • Retirement Programs through the Teacher Retirement System of Texas (TRS)

  • Paid Parental Leave Benefit

  • Wellness programs

  • Tuition Reimbursement

  • Public Service Loan Forgiveness (PSLF) Qualified Employer


EXPERIENCE AND EDUCATION
Required

  • Education Bachelor's Degree or equivalent

  • Experience 2 years of related experience
    May consider experience and education in lieu of requirements.


JOB DUTIES

  • Review study protocols, informed consent documents, response to stipulations, and other study-related documentation, to assure conformance with all applicable requirements.

  • Provide working supervision, training, and guidance to lower-level Regulatory Assistants. Assign tasks and set work priorities. Review work for accuracy.

  • Administer expedited and exempt research review processes, including, but not limited to: intake of protocols and assessment of review level (with referral to full IRB/IACUC, when applicable); regular one-on-one meetings with IRB/IACUC Chairs for final determinations; drafting correspondence to investigators regarding IRB/IACUC determinations.

  • Provide consultation and technical assistance to investigators and study personnel regarding requirements for IRB/IACUC submissions, performance of studies, and documentation of compliance. Serve as an information resource to the campus about human subject protection and/or animal care and use.

  • Participate in development of and/or updates to IRB/IACUC guidance, office procedures/business processes, related forms, database improvements, and other quality assurance activities.

  • Perform other duties as assigned.


SECURITY AND EEO STATEMENT
Security

This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.


EEO

UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.

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University of Texas Southwestern Medical Center logo

About University of Texas Southwestern Medical Center

Sourced by ZipRecruiter

The University of Texas Southwestern Medical Center (UT Southwestern), located in Dallas, Texas, United States, operates in the healthcare and higher education sectors. It's renowned as one of the leading academic medical centers globally, focusing on medical care, research, and education. Its official website is utsouthwestern.edu. Founded in 1943, it's dedicated to improving health care in their community, the region, and around the globe.

Industry

Hospitals

Company size

10,000+ Employees

Headquarters location

Dallas, TX, US

Year founded

1943