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Regulatory Affairs Specialists in South Carolina

Thinking about a career as a Regulatory Affairs Specialists in South Carolina? Below are the key facts. Examine, evaluate, and investigate eligibility for or conformity with laws and regulations governing contract compliance of licenses and permits, and perform other compliance and enforcement inspection and analysis activities not classified elsewhere. Excludes “Financial Examiners" (13-2061), “Tax Examiners and Collectors, and Revenue Agents” (13-2081), “Occupational Health and Safety Specialists” (19-5011), “Occupational Health and Safety Technicians” (19-5012), “Transportation Security Screeners” (33-9093), “Agricultural Inspectors” (45-2011), “Construction and Building Inspectors” (47-4011), and “Transportation Inspectors” (53-6051).

What do Regulatory Affairs Specialists Make in South Carolina?

For a regulatory affairs specialists working in South Carolina, the median annual wage is $76,200 per year (or about $36.64/hour).Earnings range from $43,200 at the 10th percentile to $137,080 at the 90th percentile.

Wage Statistic	Annual	Hourly
10th percentile	$43,200	$20.77
25th percentile	$55,260	$26.57
Median (50th)	$76,200	$36.64
75th percentile	$102,920	$49.48
90th percentile	$137,080	$65.90

Location quotient — how concentrated this career is in South Carolina compared to the national average — is 0.79, meaning fewer regulatory affairs specialists per worker than the national average.

National Wage Comparison

Nationally, regulatory affairs specialists earn a median of $85,399 per year ($41.06/hour), lower than the South Carolina median.

Employment Outlook

There are roughly 326,183 regulatory affairs specialists across the United States. In South Carolina alone, around 4,650 people work in this role. That’s more than the typical state, which employs around 4,100 regulatory affairs specialists.

Top South Carolina Metros for Regulatory Affairs Specialists

The largest metro-area employers of regulatory affairs specialists in South Carolina.

Metro Area	Number Employed	Annual Median Salary
Charleston-North Charleston, SC	1,250	$92,750
Columbia, SC	960	$66,020
Greenville-Anderson-Greer, SC	700	$72,860
Spartanburg, SC	210	$62,320
Myrtle Beach-Conway-North Myrtle Beach, SC	140	$64,020
Florence, SC	130	$59,190
Hilton Head Island-Bluffton-Port Royal, SC	100	$63,790
Sumter, SC	60	$71,950

Top States for Regulatory Affairs Specialists Employment

View the states that employ the most regulatory affairs specialists work.

State	Number Employed
California	47,420
Texas	39,870
Florida	31,610
New York	23,690
Pennsylvania	15,320
Virginia	15,120
Georgia	13,730
New Jersey	12,000
Arizona	11,590
Massachusetts	11,460
Ohio	11,320
Washington	10,820
Illinois	10,190
Michigan	9,660
North Carolina	9,080
Maryland	8,860
Tennessee	8,140
Colorado	7,470
Missouri	7,000
Minnesota	6,460

Highest-Paying States for Regulatory Affairs Specialists

The highest-paying states for regulatory affairs specialists.

State	Annual Median Salary
District of Columbia	$103,010
New Jersey	$93,520
Massachusetts	$92,890
California	$92,350
Alaska	$88,730
Vermont	$88,550
Delaware	$88,450
Maryland	$87,580
Connecticut	$87,210
Maine	$86,940

Skills

Key regulatory affairs specialists skills, rated on an importance scale of 0 to 5:

Knowledge Areas

Core knowledge areas for this occupation, rated on an importance scale of 0 to 5:

Abilities

Key abilities for regulatory affairs specialists, rated on an importance scale of 0 to 5:

Daily Tasks

Day-to-day, regulatory affairs specialists typically:

• Coordinate efforts associated with the preparation of regulatory documents or submissions.
• Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, or clarification and follow-up of submissions under review.
• Prepare or direct the preparation of additional information or responses as requested by regulatory agencies.
• Coordinate, prepare, or review regulatory submissions for domestic or international projects.
• Prepare or maintain technical files as necessary to obtain and sustain product approval.
• Interpret regulatory rules or rule changes and ensure that they are communicated through corporate policies and procedures.
• Determine the types of regulatory submissions or internal documentation that are required in situations such as proposed device changes or labeling changes.
• Coordinate recall or market withdrawal activities as necessary.
• Advise project teams on subjects such as premarket regulatory requirements, export and labeling requirements, or clinical study compliance issues.
• Review adverse drug reactions and file all related reports in accordance with regulatory agency guidelines.
• Review product promotional materials, labeling, batch records, specification sheets, or test methods for compliance with applicable regulations and policies.
• Identify relevant guidance documents, international standards, or consensus standards.

Work Activities

• Evaluating Information to Determine Compliance with Standards
• Getting Information
• Communicating with Supervisors, Peers, or Subordinates
• Communicating with People Outside the Organization
• Working with Computers
• Making Decisions and Solving Problems
• Interpreting the Meaning of Information for Others
• Updating and Using Relevant Knowledge
• Establishing and Maintaining Interpersonal Relationships
• Analyzing Data or Information
• Organizing, Planning, and Prioritizing Work
• Developing Objectives and Strategies

Tools & Technology

Common tools and software used in this occupation include: Hot technologies: Adobe Acrobat, Microsoft Access In-demand technologies: Microsoft Excel

What Major Will Prepare You For This Career?

Programs that train for this career include:

• Natural Resource Management
• Human Resource Management

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Related Careers

Careers similar to regulatory affairs specialists include:

• Quality Control Systems Managers
• Clinical Research Coordinators
• Regulatory Affairs Managers
• Compliance Managers
• Compliance Officers
• Environmental Compliance Inspectors

Also Known As

Anti Money Laundering Compliance Analyst (AML Compliance Analyst), CMC Regulatory Affairs Manager (Chemistry, Manufacturing, and Controls Regulatory Affairs Manager), Clinical Quality Assurance Associate, Clinical Quality Assurance Specialist, Drug Regulatory Affairs Specialist, Product Safety Specialist, Product Stewardship Specialist, Quality Assurance Documentation Coordinator, Quality Assurance Documentation Specialist, Regulatory Affairs Analyst (RA Analyst), Regulatory Affairs Associate (RA Associate), Regulatory Affairs Consultant (RA Consultant), Regulatory Affairs Coordinator (RA Coordinator), Regulatory Affairs Scientist, Regulatory Affairs Specialist (RA Specialist).

References

• U.S. Bureau of Labor Statistics, Occupational Employment and Wage Statistics — https://www.bls.gov/oes/
• O*NET Online — https://www.onetonline.org/
• BLS Employment Projections — https://www.bls.gov/emp/
• O*NET-SOC code: 13-1041.07