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Fda Regulatory Entrylevel Jobs (NOW HIRING)

Generate essential study documents (FDA 1572, Financial Disclosure Forms, etc.) * Report deviations ... Associate degree preferred * Entry-level experience in a clinical research environment required

Generate essential study documents (FDA 1572, Financial Disclosure Forms, etc.) * Report deviations ... Associate degree preferred * Entry-level experience in a clinical research environment required

We also welcome entry level candidates who are eager to learn. Duties * Coordinate and manage all ... Ensure compliance with international trade laws, FDA regulations (Food and Drug Administration ...

Position Summary Able to perform entry level inspection, repetitive tasks associated with visual ... Demonstrated knowledge with medical device regulations and FDA regulatory standards preferred.

Position Summary Able to perform entry level inspection, repetitive tasks associated with visual ... Demonstrated knowledge with medical device regulations and FDA regulatory standards preferred.

$70K - $85K/yr

This entry-level role offers the opportunity to gain hands-on experience in a dynamic, GMP ... Familiar with regulatory (FDA) requirements. * Business minor or coursework is strongly encouraged.

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How much do fda regulatory entrylevel jobs pay per year?

As of Jun 15, 2026, the average yearly pay for fda regulatory entrylevel in the United States is $110,733.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $136,500.00 per year, depending on experience, location, and employer.

Is it hard to get hired by the FDA?

Getting hired as an entry-level FDA regulatory professional can be competitive due to the specialized knowledge required, such as understanding regulatory guidelines and documentation processes. Candidates often need relevant education, certifications, and sometimes prior experience in the industry to improve their chances of employment.

How to get into regulatory affairs with no experience?

Entering an entry-level FDA regulatory affairs role typically requires a bachelor's degree in a relevant field such as life sciences, healthcare, or engineering. Gaining knowledge of regulations through online courses, certifications like RAC, and developing skills in documentation, compliance, and communication can improve prospects; internships or volunteer work in related areas also help build experience.

How to start a career in regulatory affairs?

To start a career in regulatory affairs, obtain a relevant degree such as life sciences, pharmacy, or engineering, and gain knowledge of industry regulations like FDA or EMA standards. Entry-level roles often require strong attention to detail, communication skills, and familiarity with regulatory submission processes; certifications such as RAC can enhance prospects.

What qualifications do you need to work for the FDA?

To work as an FDA regulatory entry-level professional, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or health sciences. Knowledge of regulatory policies, good communication skills, and familiarity with FDA guidelines are also important; some roles may require specific certifications or training in regulatory affairs.
More about Fda Regulatory Entrylevel jobs
What cities are hiring for Fda Regulatory Entrylevel jobs? Cities with the most Fda Regulatory Entrylevel job openings:
What states have the most Fda Regulatory Entrylevel jobs? States with the most job openings for Fda Regulatory Entrylevel jobs include:
What job categories do people searching Fda Regulatory Entrylevel jobs look for? The top searched job categories for Fda Regulatory Entrylevel jobs are:
Infographic showing various Fda Regulatory Entrylevel job openings in the United States as of June 2026, with employment types broken down into 38% Full Time, and 62% Contract. Highlights an 87% In-person, and 13% Remote job distribution, with an average salary of $110,733 per year, or $53.2 per hour.
Regulatory Affairs Specialists (Life Sciences)

Regulatory Affairs Specialists (Life Sciences)

University of Utah

Salt Lake City, UT • On-site

$25K/mo

Full-time

Medical, Retirement, PTO

Posted 12 days ago


University Of Utah rating

7.2

Company rating: 7.2 out of 10

Based on 157 frontline employees who took The Breakroom Quiz

335th of 537 rated colleges and universities


Job description

Announcement
Details
Open Date
06/03/2026
Requisition Number
PRN45245B
Job Title
Regulatory Affairs Specialists (Life Sciences)
Working Title
Regulatory Specialist
Career Progression Track
P00
Track Level
P4 - Advanced, P3 - Career, P2 - Developing, P1 - Entry Level Pro
FLSA Code
Administrative
Patient Sensitive Job Code?
Yes
Standard Hours per Week
40
Full Time or Part Time?
Full Time
Shift
Day
Work Schedule Summary
Monday - Friday, 8:00 a.m. - 5:00 p.m. Hours may vary based on operational needs.
Opportunities for a hybrid telework schedule may be considered after the initial training period, provided the arrangement is supported by operational needs and individual performance. Telework arrangements are not guaranteed and may be modified or discontinued at any time based on business requirements or performance. Employees approved for hybrid telework must provide their own private workspace, secure internet connection, and demonstrate the ability to work independently.
VP Area
U of U Health - Academics
Department
00848 - Pediatric Administration
Location
Campus
City
Salt Lake City, UT
Type of Recruitment
External Posting
Pay Rate Range
Depends on Experience
Close Date
09/03/2026
Priority Review Date (Note - Posting may close at any time)
Job Summary
Job Summary:
The Division of Neurology in the Department of Pediatrics is seeking a Regulatory Affairs Specialist to support clinical research activities at the University of Utah Spencer F. Eccles School of Medicine. This position is responsible for preparing, submitting, and tracking regulatory documents to ensure compliance with institutional, federal, and sponsor requirements. The Regulatory Affairs Specialist will collaborate with study teams, institutional review boards (IRB), and external sponsors to support study start-up, maintenance, and closeout activities.
The role involves maintaining regulatory documentation, supporting audits and inspections, and ensuring adherence to applicable regulations and guidelines. The incumbent will also assist in monitoring regulatory changes and communicating updates to study teams to support ongoing compliance.
This position is posted at multiple job levels. Each level has distinct qualifications, responsibilities, which will be evaluated during the selection process. Final placement, including the associated pay rate, will be determined based on business needs and budget considerations.
Department Summary:
The Department of Pediatrics is the second largest department in the University of Utah School of Medicine and one of the largest pediatric departments in the country. We are committed to improving the lives of children through excellence in advocacy, education, research, and clinical care. For more information about the Department of Pediatrics, please visit:http://medicine.utah.edu/pediatrics/. Mutual respect and appreciation are highly valued in the department.
Benefits Summary:
The University of Utah offers a comprehensive benefits package including:
  • Excellent health care coverage at affordable rates (see the Summary Comparison for more information)
  • 14.2% retirement contributions
  • Generous paid leave time
  • 11 paid Holidays per year
  • 50% tuition reduction for employees, spouses, and dependent children
  • Flex spending accounts
  • University provided basic employee life insurance coverage equal to a salary of up to $25,000
  • Variety of elective insurance coverage, including life insurance, short and long-term disability, accidental death & dismemberment, accident, critical illness, hospital indemnity, and pet.
  • Free transit on most UTA services
  • Employee discounts on a variety of products and services, including cell phones & plans, entertainment, health and fitness, restaurants, retail, and travel
  • Professional development opportunities

Additional benefits information is available at https://benefits.utah.edu/.
Employee Health Requirements:
This position is patient-sensitive and must fulfill all associated vaccination requirements, or be approved for an exemption, prior to the first day of work. We protect our patients, coworkers and community by requiring all patient-sensitive employees to be immunized according to CDC standards and hospital policy. Limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations.
Responsibilities
Essential Functions:
Prepare, submit, and track regulatory documents and submissions. Ensure submissions are complete, timely, and regulatory objectives are met. Research scientific and regulatory information in order to write, edit, and review reports. Work with various governmental and regulatory bodies (e.g., FDA, MHRA, EMA) to ensure compliance and expedite approval of pending registration. Compile all material required for submissions, license renewals, and annual registrations. Identify relevant guidance documents and interpret international/consensus standards. Participate in internal or external audits and inspections.
1. Prepare and submit IRB applications, amendments, and reports to support study start-up and ongoing compliance.
2. Track IRB submissions, complete required revisions, and ensure adherence to established timelines.
3. Prepare and maintain study training logs and regulatory documentation (e.g., DOA logs).
4. Manage and maintain regulatory binders/ISF and associated study documentation.
5. Ensure all regulatory documents, certifications, and licenses are current and maintained.
6. Monitor updates to University of Utah IRB policies and processes and apply changes to study activities.
7. Communicate regulatory and IRB updates to study teams to ensure ongoing compliance.
8. Review and maintain familiarity with active study protocols to support regulatory requirements.
9. Collaborate with study teams and sponsors to finalize regulatory documents (e.g., ICFs).
10. Ensure timely completion of regulatory submissions and revisions in accordance with study timelines.
11. Assist in the development and maintenance of internal SOPs, as needed.
12. Assist with additional regulatory or study-related tasks as needed to support compliance and operational objectives.
The following job levels and associated pay rates will be considered based on job placement. Final placement, including the corresponding pay rate, will be determined by the department in alignment with business needs and budget considerations.
Regulatory Affairs Specialist (Life Sciences), I
Requires basic skill set and proficiency. Conducts work assignments as directed. Closely supervised with little latitude for independent judgment.
Requires a bachelor's (or equivalency) with up to 2 years of directly related work experience or a master's (or equivalency) degree.
This is an Entry-Level position in the General Professional track.
Job Code: PZ6891
Grade: P13
Expected Pay Range: $46,584 to $57,976
Regulatory Affairs Specialist (Life Sciences), II
Requires moderate skill set and proficiency in discipline. Conducts work assignments of increasing complexity, under moderate supervision with some latitude for independent judgment.
Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience.
This is a Developing-Level position in the General Professional track.
Job Code: PZ6892
Grade: P14
Expected Pay Range: $51,242 to $69,629
Regulatory Affairs Specialist (Life Sciences), III
Considered highly skilled and proficient in discipline. Conducts complex, important work under minimal supervision and with wide latitude for independent judgment.
Requires a bachelor's (or equivalency) + 6 years or a master's (or equivalency) + 4 years of directly related work experience.
This is a Career-Level position in the General Professional track.
Job Code: PZ6893
Grade: P16
Expected Pay Range: $62,004 to $84,252
Regulatory Affairs Specialist (Life Sciences), IV
Recognized as subject matter expert and advanced individual contributor professional. Requires specialized skill set. Conducts highly complex work, unsupervised and with extensive latitude for independent judgment.
Requires a bachelor's (or equivalency) + 8 years or a master's (or equivalency) + 6 years of directly related work experience.
This is an Advanced-Level position in the General Professional track.
Job Code: PZ6894
Grade: P17
Expected Pay Range: $68,204 to $92,678
Disclaimer:
This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.
Minimum Qualifications
EQUIVALENCY STATEMENT: 1 year of higher education can be substituted for 1 year of directly related work experience (Example: bachelor's degree = 4 years of directly related work experience).
Department may hire employee at one of the following job levels:
Regulatory Affairs Specialist (Life Sciences), I: Requires a bachelor's (or equivalency) + 2 years of directly related work experience or a master's (or equivalency) degree.
Regulatory Affairs Specialist (Life Sciences), II: Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience.
Regulatory Affairs Specialist (Life Sciences), III: Requires a bachelor's (or equivalency) + 6 years or a master's (or equivalency) + 4 years of directly related work experience.
Regulatory Affairs Specialist (Life Sciences), IV: Requires a bachelor's (or equivalency) + 8 years or a master's (or equivalency) + 6 years of directly related work experience.
Preferences
Preferences:
  • Experience with University of Utah IRB.
  • Clinical research regulatory experience.
  • CITI Training (or to be completed within 1 month of hire).

The Department will screen applicants according to the identified preferences.
Type
Benefited Staff
Special Instructions Summary
Additional Information
The University is a participating employer with Utah Retirement Systems ("URS"). Eligible new hires with prior URS service, may elect to enroll in URS if they make the election before they become eligible for retirement (usually the first day of work). Contact Human Resources at (801) 581-7447 for information. Individuals who previously retired and are receiving monthly retirement benefits from URS are subject to URS' post-retirement rules and restrictions. Please contact Utah Retirement Systems at (801) 366-7770 or (800) 695-4877 or University Human Resource Management at (801) 581-7447 if you have questions regarding the post-retirement rules.
This position may require the successful completion of a criminal background check and/or drug screen.
The University of Utah values candidates who have experience working in settings with students and possess a strong commitment to improving access to higher education.
Veterans' preference is extended to qualified applicants, upon request and consistent with University policy and Utah state law. Upon request, reasonable accommodations in the application process will be provided to individuals with disabilities.
Consistent with state and federal law, the University of Utah does not discriminate based upon race, ethnicity, color, religion, national origin, age, disability, sex, sexual orientation, gender, gender identity, gender expression, pregnancy, pregnancy-related conditions, genetic information, or protected veteran's status. The University does not discriminate on the basis of sex in the education program or activity that it operates, as required by Title IX and 34 CFR part 106. The requirement not to discriminate in education programs or activities extends to admission and employment. Inquiries about the application of Title IX and its regulations may be referred to the Title IX Coordinator, to the Department of Education, Office for Civil Rights, or both.
To request a reasonable accommodation for a disability or if you or someone you know has experienced discrimination or sexual misconduct including sexual harassment, you may contact the Director/Title IX Coordinator in the Office of Equal Opportunity and Title IX (OEO). More information, including the Director/Title IX Coordinator's office address, electronic mail address, and telephone number can be located at the: University of Utah Non-Discrimination page.
Online reports may be submitted at https://oeo.utah.edu
https://publicsafety.utah.edu/safetyreport/ This report includes statistics about criminal offenses, hate crimes, arrests and referrals for disciplinary action, and Violence Against Women Act offenses. They also provide information about safety and security-related services offered by the University of Utah. A paper copy can be obtained by request at the Department of Public Safety located at 1658 East 500 South.
As per University of Utah policy 5-108: Transfer of Benefits Eligible Staff Members, a new hire to the Univ...

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About University of Utah

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The University of Utah is the state’s flagship institution of higher education, with 18 schools and colleges, more than 100 undergraduate majors and graduate programs, and an enrollment of more than 38,000 students. It is a member of the Association of American Universities—an invitation-only, prestigious group of 71 leading research institutions. The U is advancing a new national model for higher education that delivers societal impact through education, research, health care, and community service, while making social, economic, and cultural contributions that improve lives across Utah and around the world.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Salt Lake City, UT, US

Year founded

1850