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 ...
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 ...
Associate Director, Regulatory Affairs & Submissions - Nonclinical Development
Columbia, MO · On-site
About the Role The Associate Director, Regulatory Affairs - Nonclinical Development is a strategic regulatory leader specializing in nonclinical drug development. This role is responsible for guiding ...
Associate Director, Regulatory Affairs & Submissions - Nonclinical Development
Columbia, MO · On-site
About the Role The Associate Director, Regulatory Affairs - Nonclinical Development is a strategic regulatory leader specializing in nonclinical drug development. This role is responsible for guiding ...
Associate Director or Director, Regulatory Strategy (Clinical & Nonclinical) Department: Regulatory Reports To: VP of Regulatory Location: Remote or Onsite Position Summary: The Associate Director ...
Quick apply
Associate Director or Director, Regulatory Strategy (Clinical & Nonclinical) Department: Regulatory Reports To: VP of Regulatory Location: Remote or Onsite Position Summary: The Associate Director ...
Clinical Operations & Program Management * Clinical Sciences * Regulatory Strategy * Regulatory Labeling & Advertising/Promotion * Safety Sciences Associates will also have opportunities to gain ...
Clinical Operations & Program Management * Clinical Sciences * Regulatory Strategy * Regulatory Labeling & Advertising/Promotion * Safety Sciences Associates will also have opportunities to gain ...
Clinical Operations & Program Management * Clinical Sciences * Regulatory Strategy * Regulatory Labeling & Advertising/Promotion * Safety Sciences Associates will also have opportunities to gain ...
Clinical Operations & Program Management * Clinical Sciences * Regulatory Strategy * Regulatory Labeling & Advertising/Promotion * Safety Sciences Associates will also have opportunities to gain ...
We are now recruiting an Associate Director, R&I Clinical Regulatory Writing (CReW). As part of a clinical delivery or submission team, the Associate Director provides strategic communications ...
We are now recruiting an Associate Director, R&I Clinical Regulatory Writing (CReW). As part of a clinical delivery or submission team, the Associate Director provides strategic communications ...
We are now recruiting an Associate Director, R&I Clinical Regulatory Writing (CReW). As part of a clinical delivery or submission team, the Associate Director provides strategic communications ...
We are now recruiting an Associate Director, R&I Clinical Regulatory Writing (CReW). As part of a clinical delivery or submission team, the Associate Director provides strategic communications ...
Clinical Operations & Program Management * Clinical Sciences * Regulatory Strategy * Regulatory Labeling & Advertising/Promotion * Safety Sciences Associates will also have opportunities to gain ...
Clinical Operations & Program Management * Clinical Sciences * Regulatory Strategy * Regulatory Labeling & Advertising/Promotion * Safety Sciences Associates will also have opportunities to gain ...
The Regulatory Associate Senior will be primarily responsible for regulatory support of a specific ... Regulatory experience in Clinical Research strongly preferred. BENEFITS UT Southwestern is proud to ...
The Regulatory Associate Senior will be primarily responsible for regulatory support of a specific ... Regulatory experience in Clinical Research strongly preferred. BENEFITS UT Southwestern is proud to ...
The Regulatory Associate Senior will be primarily responsible for regulatory support of a specific ... Regulatory experience in Clinical Research strongly preferred. BENEFITS UT Southwestern is proud to ...
The Regulatory Associate Senior will be primarily responsible for regulatory support of a specific ... Regulatory experience in Clinical Research strongly preferred. BENEFITS UT Southwestern is proud to ...
Associate Director, R&I Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$136K - $205K/yr
The Associate Director also authorsstrategic clinical-regulatory documents and providescritical review to achieve high-quality standards,utilizingbest practices for document and accelerated ...
Associate Director, R&I Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$136K - $205K/yr
The Associate Director also authorsstrategic clinical-regulatory documents and providescritical review to achieve high-quality standards,utilizingbest practices for document and accelerated ...
The Regulatory Associate Senior will be primarily responsible for regulatory support of a specific ... Regulatory experience in Clinical Research strongly preferred. BENEFITS UT Southwestern is proud to ...
The Regulatory Associate Senior will be primarily responsible for regulatory support of a specific ... Regulatory experience in Clinical Research strongly preferred. BENEFITS UT Southwestern is proud to ...
The Associate Director also authorsstrategic clinical-regulatory documents and providescritical review to achieve high-quality standards,utilizingbest practices for document and accelerated ...
The Associate Director also authorsstrategic clinical-regulatory documents and providescritical review to achieve high-quality standards,utilizingbest practices for document and accelerated ...
Senior Consultant- Clinical & Regulatory Information Management US Apply now Details Type of ... the Associate Vice President of the department. As a member of our team, you can count on ...
Senior Consultant- Clinical & Regulatory Information Management US Apply now Details Type of ... the Associate Vice President of the department. As a member of our team, you can count on ...
Support the development and execution of clinical regulatory strategies for assigned programs under the direction of senior regulatory leadership, including contributing analyses, options, and ...
Support the development and execution of clinical regulatory strategies for assigned programs under the direction of senior regulatory leadership, including contributing analyses, options, and ...
Support the development and execution of clinical regulatory strategies for assigned programs under the direction of senior regulatory leadership, including contributing analyses, options, and ...
Support the development and execution of clinical regulatory strategies for assigned programs under the direction of senior regulatory leadership, including contributing analyses, options, and ...
Support the development and execution of clinical regulatory strategies for assigned programs under the direction of senior regulatory leadership, including contributing analyses, options, and ...
Quick apply
Support the development and execution of clinical regulatory strategies for assigned programs under the direction of senior regulatory leadership, including contributing analyses, options, and ...
AD/ Director, Clinical Regulatory Affairs Gene Therapy
Malvern, PA · On-site
$147K - $194K/yr
Position Summary The Associate Director, Regulatory Affairs - Gene Therapy will play a highly visible role in advancing Ocugen's clinical-stage gene therapy programs through critical phases of ...
AD/ Director, Clinical Regulatory Affairs Gene Therapy
Malvern, PA · On-site
$147K - $194K/yr
Position Summary The Associate Director, Regulatory Affairs - Gene Therapy will play a highly visible role in advancing Ocugen's clinical-stage gene therapy programs through critical phases of ...
AD/ Director, Clinical Regulatory Affairs Gene Therapy
Malvern, PA · On-site
$147K - $194K/yr
Position Summary The Associate Director, Regulatory Affairs - Gene Therapy will play a highly visible role in advancing Ocugen's clinical-stage gene therapy programs through critical phases of ...
AD/ Director, Clinical Regulatory Affairs Gene Therapy
Malvern, PA · On-site
$147K - $194K/yr
Position Summary The Associate Director, Regulatory Affairs - Gene Therapy will play a highly visible role in advancing Ocugen's clinical-stage gene therapy programs through critical phases of ...
From clinical trials to regulatory, consulting, and market access, every clinical development ... The Regulatory Affairs Generalist / Senior Associate provides comprehensive support across clinical ...
From clinical trials to regulatory, consulting, and market access, every clinical development ... The Regulatory Affairs Generalist / Senior Associate provides comprehensive support across clinical ...
Clinical Regulatory Associate information
See salary details
$12.74 - $16.61
3% of jobs
$16.61 - $20.48
18% of jobs
$21.24 is the 25th percentile. Wages below this are outliers.
$20.48 - $24.34
20% of jobs
The median wage is $26.69 / hr.
$24.34 - $28.21
15% of jobs
$28.21 - $32.08
11% of jobs
$32.08 - $35.95
4% of jobs
$39.24 is the 75th percentile. Wages above this are outliers.
$35.95 - $39.82
5% of jobs
$39.82 - $43.68
8% of jobs
$43.68 - $47.55
6% of jobs
$47.55 - $51.42
6% of jobs
$51.42 - $55.29
3% of jobs
$12
$31
$55
How much do clinical regulatory associate jobs pay per hour?
What does a clinical regulatory associate do?
What cities are hiring for Clinical Regulatory Associate jobs?
Cities with the most Clinical Regulatory Associate job openings:
What are the most commonly searched types of Clinical Regulatory jobs?
The most popular types of Clinical Regulatory jobs are:
What are popular job titles related to Clinical Regulatory Associate jobs?
For Clinical Regulatory Associate jobs, the most frequently searched job titles are:
Regulatory Associate, Simmons Cancer Center
Dallas, TX • On-site
Full-time
Medical, Retirement, PTO
Posted 11 days ago
UT Southwestern rating
7.9
Based on 152 frontline employees who took The Breakroom Quiz
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
- 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.
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.
What UT Southwestern employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About UT Southwestern
Sourced by ZipRecruiter
Industry
Hospitals
Company size
10,000+ Employees
Headquarters location
Dallas, TX, US
Year founded
1943