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Regulatory Associate, Neurosurgery

UT Southwestern Medical Center
Posted 8 months ago, valid for 8 days
Location

Dallas, TX 75320, US

Salary

Competitive

Contract type

Full Time

Paid Time Off
Tuition Reimbursement
Wellness Program

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Sonic Summary

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  • UT Southwestern is seeking a Regulatory Associate for the Neurosurgery Research Group, requiring a Bachelor's Degree and 2 years of related experience.
  • The role involves overseeing regulatory compliance for various clinical research projects, including trials funded by NIH and industry sponsors.
  • The position offers a competitive salary and a comprehensive benefits package, including healthcare, paid time off, and retirement programs.
  • Preferred qualifications include experience with Central IRB applications, local IRB submissions, and FDA applications.
  • UT Southwestern is committed to a diverse and inclusive work environment, providing equal opportunity to all employees.

Regulatory Associate - Neurosurgery Department

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
The Department of Neurological Surgery is seeking a Regulatory Associate to join its central research team, the Neurosurgery Research Group (NRG). The Regulatory Associate will oversee the regulatory compliance of NRG’s diverse clinical research portfolio, including investigator-initiated trials, NIH-funded studies, FDA IDE trials, industry-sponsored drug and device trials, and sIRB studies where we serve as the IRB of record.

 

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%25 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
  • Learn more about these and other UTSW employee benefits!



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. 
     

Preferred

  • Experience
    Previous experience with Central IRB Applications 

     

    Previous Experience with Local IRB Submissions 

     

    Previous experience with eFlorence or a similar physical or electronic regulatory binder maintenance 

     

    Previous experience with FDA applications and amendments 

     

    Previous Performance Site Review Experience


     


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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