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Regulatory Affairs Analyst Jobs (NOW HIRING)

InstantServe LLC

Regulatory Affairs Analyst

Parsippany, NJ · On-site

$50 - $70/hr

Regulatory Affairs Analyst HM: Lia Gonzalez Pay Rate: $50-70/per hour.(Targeting more towards the $50s) Type: Hybrid (2 days Onsite) Must be onsite every Wednesday and can choose between Tuesday and ...

UDR Inc

Governmental Affairs Analyst

Littleton, CO

$68.80K - $76.40K/yr

UDR, Inc. is now hiring a Governmental Affairs Analyst to join our team at our corporate office in ... N/A ESSENTIAL FUNCTIONS: 1. Develop advanced knowledge of regulatory frameworks through research ...

UDR

Governmental Affairs Analyst

Highlands Ranch, CO

$68.80K - $76.40K/yr

UDR, Inc. is now hiring a Governmental Affairs Analyst to join our team at our corporate office in ... N/A ESSENTIAL FUNCTIONS: 1. Develop advanced knowledge of regulatory frameworks through research ...

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How much do regulatory affairs analyst jobs pay per hour?

As of May 28, 2026, the average hourly pay for regulatory affairs analyst in the United States is $46.85, according to ZipRecruiter salary data. Most workers in this role earn between $37.74 and $53.85 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Regulatory Affairs Analyst, and why are they important?

To thrive as a Regulatory Affairs Analyst, you need a solid background in regulatory guidelines, compliance, and scientific or legal knowledge, often backed by a degree in life sciences, pharmacy, or a related field. Familiarity with regulatory databases, document management systems, and certifications like RAC (Regulatory Affairs Certification) are highly valued. Strong analytical thinking, attention to detail, and effective communication skills help professionals excel in interpreting regulations and liaising with multiple stakeholders. These skills ensure that products meet legal standards and market requirements, minimizing risk and facilitating smooth regulatory approvals.

How does a Regulatory Affairs Analyst typically collaborate with cross-functional teams within an organization?

Regulatory Affairs Analysts work closely with departments such as research and development, quality assurance, clinical operations, and manufacturing to ensure that products comply with relevant regulations. They often facilitate communication between these teams to gather necessary documentation, interpret guidelines, and address compliance issues. This collaboration is essential for preparing regulatory submissions, responding to agency questions, and implementing regulatory changes efficiently. Strong interpersonal and organizational skills are vital for successful cross-functional teamwork in this role.

What does a Regulatory Affairs Analyst do?

A Regulatory Affairs Analyst is responsible for ensuring that a company complies with all regulations and laws relevant to its business. They prepare and submit documentation to regulatory agencies, monitor changes in regulations, and advise on compliance strategies. Their work is particularly important in industries like pharmaceuticals, biotechnology, and medical devices, where regulatory compliance is critical. Regulatory Affairs Analysts also coordinate with other departments to ensure that products meet legal standards and are approved for market.

What is the difference between Regulatory Affairs Analyst vs Quality Assurance Analyst?

AspectRegulatory Affairs AnalystQuality Assurance Analyst
Required CredentialsBachelor's in life sciences, certifications like RAC often preferredBachelor's in related fields, certifications like CQE may be advantageous
Work EnvironmentRegulatory agencies, pharmaceutical, biotech companiesManufacturing, pharmaceutical, healthcare companies
Employer & Industry UsageFocuses on compliance with regulations and submissionsFocuses on product quality, testing, and process improvements

While both roles require knowledge of industry standards and compliance, Regulatory Affairs Analysts primarily handle regulatory submissions and compliance documentation, whereas Quality Assurance Analysts focus on product quality testing and process improvements. Both roles are essential in regulated industries like pharmaceuticals and biotech, but they serve different functions within the product lifecycle.

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What cities are hiring for Regulatory Affairs Analyst jobs? Cities with the most Regulatory Affairs Analyst job openings:
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Regulatory Affairs Analyst jobs near you
Infographic showing various Regulatory Affairs Analyst job openings in the United States as of May 2026, with employment types broken down into 56% Full Time, 31% Part Time, and 13% Contract. Highlights an 76% Physical, 3% Hybrid, and 21% Remote job distribution, with an average salary of $97,449 per year, or $46.9 per hour.
Regulatory Affairs Analyst

Regulatory Affairs Analyst

Calculated Hire

Virginia, MN • Remote

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Technical Recruiter @ Calculated Hire | Ethical Advertising, Communication Regulatory Affairs Analyst Remote 1-YR Contract (possibility of extension) Virginia, USA Overview: Our client is seeking a Regulatory Affairs Specialist to assess and enhance regulatory affairs processes, focusing on the preparation and submission of PMTA and SE applications in compliance with FDA requirements. In this role, you will conduct current state assessments, develop detailed process flow documentation, identify gaps or inefficiencies, and recommend modernization initiatives. You will collaborate closely with cross-functional teams to ensure alignment with regulatory standards and modernization goals.

The ideal candidate will have strong experience with FDA regulatory frameworks, hands‐on expertise in eCTD/dossier preparation, and familiarity with regulatory information management systems such as Veeva RIM. Excellent analytical, communication, and stakeholder engagement skills are essential for success in this position. Responsibilities: Conduct current state assessments of regulatory affairs processes and workflows with key stakeholders.

Develop detailed process flow documentation and identify gaps or inefficiencies. Analyze opportunity areas and provide recommendations for modernization initiatives. Support preparation and submission of PMTA and SE applications in compliance with FDA requirements.

Collaborate with cross-functional teams to ensure alignment with regulatory standards and modernization goals. Qualifications: Proven experience in regulatory affairs, including PMTA and SE application processes. Strong knowledge of FDA regulatory frameworks and compliance requirements.

Hands‐on experience with eCTD/dossier preparation and submission. Familiarity with Veeva RIM or similar regulatory information management systems. Excellent analytical, communication, and stakeholder engagement skills.

Flexible remote work environment Opportunity to drive modernization initiatives in regulatory affairs Collaborative and cross‐functional team culture Competitive hourly compensation Seniority Level Associate Employment Type Full-time Job Function Legal and Research Industries Legal Services and Tobacco Manufacturing #J-18808-Ljbffr

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