$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
$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
$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
$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
Edgewood, KY · On-site
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 ...
Edgewood, KY · On-site
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 ...
Edgewood, KY · On-site
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 ...
Edgewood, KY · On-site
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 ...
| Aspect | Associate Irb Administrator | Research Coordinator |
|---|---|---|
| Credentials | Typically requires a bachelor's degree, familiarity with IRB processes | Usually holds a bachelor's degree, often in health or science fields |
| Work Environment | Works within IRB offices, focusing on protocol review and compliance | Works directly with research participants and study teams |
| Employer & Industry | Research institutions, hospitals, universities | Research sites, hospitals, academic institutions |
| Common Search & Comparison | Often compared for roles supporting IRB functions | Compared 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.
On-site
$65 - $90/hr
Other
Medical, Retirement, PTO
Posted 21 hours ago
Posted today
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!
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.
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:
This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.
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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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.
Hospitals
10,000+ Employees
Dallas, TX, US
1943