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How much do regulatory affairs associate jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for regulatory affairs associate in Indiana is $37.65, according to ZipRecruiter salary data. Most workers in this role earn between $30.19 and $44.62 per hour, depending on experience, location, and employer.

What is a regulatory affairs associate?

A regulatory affairs associate helps medical and pharmaceutical companies navigate regulatory approval processes so that products conform to all local, state, and federal regulations. As a regulatory affairs associate, you work with a team to obtain approval for products, maintain database systems for relevant information, and create reports required by federal or government agencies. You stay abreast of developments in legislation and regulation that may affect your company, and advise others on best practices for product development within a regulated framework.

What are the key skills and qualifications needed to thrive as a regulatory affairs associate, and why are they important?

To thrive as a Regulatory Affairs Associate, you need a solid background in life sciences or related fields, attention to detail, and knowledge of regulatory guidelines and standards. Familiarity with submission management systems, regulatory databases, and certifications such as RAC (Regulatory Affairs Certification) are highly valued. Strong organizational skills, effective communication, and the ability to work collaboratively are important soft skills in this role. These abilities ensure accurate documentation, timely regulatory submissions, and successful navigation of complex compliance requirements.

What are some common challenges regulatory affairs associates face when coordinating with cross-functional teams?

Regulatory Affairs Associates often collaborate closely with departments such as research and development, quality assurance, and marketing. A common challenge is ensuring all stakeholders understand and adhere to regulatory requirements, which may change frequently. Balancing project timelines with the need for accurate and compliant documentation can also be demanding, especially when teams have competing priorities. Effective communication and proactive planning are key to navigating these challenges successfully.
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Regulatory Affairs Associate jobs near you
Infographic showing various Regulatory Affairs Associate job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $78,320 per year, or $37.7 per hour.

Global Regulatory Lead, Regulatory Strategy - Global Regulatory Affairs - Infectious Disease/Vaccine

Scorpion Therapeutics

Indianapolis, IN • On-site

$180 - $260/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago

Job description

About The Role

As the Global Regulatory Lead (GRL), you will be the accountable decision maker for the development & execution of global regulatory strategies—from portfolio entry through end of life. You will provide strategic and technical leadership to a cross-functional Global Regulatory Team, serve as the primary regulatory voice on the Global Brand Development (GBD) team, and own the relationship and interaction strategy with the US FDA.

Key Responsibilities
  • Develop and execute innovative global regulatory strategies, owning the Regulatory Strategy Document (RSD) from Candidate Selection through end of lifecycle
  • Integrate competitive intelligence, health authority guidance, and product-specific regulatory advice
  • Lead regulatory representation on the GBD/global program team; shape development plans and address regulatory barriers
  • Ensure local affiliate regulatory plans align to global strategy and business priorities (labeling, risk management, issues management)
  • Oversee US FDA submissions and agency interactions (INDs, NDAs, BLAs)
  • Drive high-quality communications with FDA articulating scientific position
  • Build relationships with FDA to support product registration goals
  • Provide strategic direction to a cross-functional Global Regulatory Team (regional scientists, GRA-CMC, GRA-Devices, GRA-RD&E, Global Labeling)
  • Foster transparent communication, feedback, and continuous development
  • Represent GRA at stakeholder/governance meetings; mentor GRA personnel
  • Build external stakeholder relationships; advise promotional strategy and review press/IR materials
Minimum Qualifications
  • Advanced scientific degree (PharmD, PhD) and 8+ years in regulatory affairs and/or drug development
  • OR
  • Bachelor’s or Masters and 10+ years in regulatory affairs and/or drug development
Additional Preferences
  • Global regulatory procedures knowledge; experience across US, EU, China, Japan
  • Clinical and CMC regulatory science experience
  • Leadership, negotiation, and executive-level communication skills
  • Risk assessment/management experience; therapeutic area experience
Additional Information
  • Travel: 10–15%
Benefits (as stated)
  • Eligibility for company-sponsored 401(k), pension, vacation; medical/dental/vision/prescription; flexible benefits; life insurance; time off/leave; well-being benefits.
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