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Regulatory Associate Jobs in Silver Spring, MD (NOW HIRING)

Pharmaron

Clinical Regulatory Associate

Baltimore, MD · On-site

$50K - $65K/yr

Clinical Regulatory Associate Location: Pharmaron Baltimore Campus, Baltimore About Pharmaron Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new ...

Pharmaron

Clinical Regulatory Associate

Baltimore, MD · On-site

$50K - $54K/yr

Clinical Regulatory Associate Location: Pharmaron Baltimore Campus, Baltimore About Pharmaron Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new ...

Pharmaron

Clinical Regulatory Associate

Baltimore, MD · On-site

$50K - $54K/yr

Clinical Regulatory Associate Location: Pharmaron Baltimore Campus, Baltimore About Pharmaron Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new ...

5 Legal

Corporate Regulatory Associate

Washington, DC · On-site

Am Law top 100 and ranked a Top 10 M&A firm across all industries is seeking a mid-level associate to join their Fintech practice. The ideal candidate will have 2-6 years of regulatory and payments ...

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Regulatory Associate information

See Silver Spring, MD salary details

$17

$33

$50

How much do regulatory associate jobs pay per hour?

As of May 28, 2026, the average hourly pay for regulatory associate in Silver Spring, MD is $33.19, according to ZipRecruiter salary data. Most workers in this role earn between $25.29 and $39.38 per hour, depending on experience, location, and employer.

What Does a Regulatory Associate Do?

As a regulatory associate or regulatory affairs associate, your job is to coordinate compliance with internal—and occasionally external—regulations. This work involves checking each inspection review for accuracy, using safety data sheets (SDS), gathering and compiling documentation for products, and submitting material for license renewals and registrations. In this role, you often create management templates, study existing report documents, oversee the collection of consent forms, and audit the company for any sign of regulatory noncompliance. Some regulatory associates frequently travel to perform audits at various locations. Depending on the industry, you may have additional tasks that involve meeting state or federal guidelines.

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

To thrive as a Regulatory Associate, you need strong attention to detail, knowledge of regulatory guidelines (such as FDA or EMA), and a relevant degree in life sciences or a related field. Familiarity with regulatory submission systems, document management tools, and electronic common technical document (eCTD) software is typically required. Excellent organizational skills, communication abilities, and the capacity to manage deadlines make candidates stand out. These skills ensure accurate regulatory submissions, compliance with evolving regulations, and effective collaboration across teams, all of which are crucial for product approvals and market access.

What are some common challenges Regulatory Associates face when working with cross-functional teams?

Regulatory Associates often work closely with teams from R&D, quality assurance, clinical, and legal departments to ensure compliance throughout product development and approval processes. A common challenge is navigating differing priorities and timelines among these groups, which requires strong communication and organizational skills. Additionally, Regulatory Associates must interpret and clarify complex regulatory requirements to various stakeholders, ensuring everyone is aligned and informed. Building collaborative relationships and proactively addressing potential misunderstandings are key to overcoming these challenges.

What is a Regulatory Associate?

A Regulatory Associate is a professional who supports regulatory affairs teams in ensuring that a company complies with all relevant laws and regulations, particularly in industries like pharmaceuticals, biotechnology, and medical devices. They assist in preparing, submitting, and maintaining regulatory filings and documentation required by government agencies. Regulatory Associates also help track changes in regulations and support product development by ensuring all necessary approvals are obtained for products to enter the market.

What is the difference between Regulatory Associate vs Compliance Specialist?

AspectRegulatory AssociateCompliance Specialist
Required CredentialsBachelor's degree in life sciences, regulatory affairs, or related field; certifications like RAC are a plusBachelor's degree in law, business, or related; certifications like CCEP may be relevant
Work EnvironmentPharmaceutical, biotech, or medical device companies; regulatory departmentsCorporate compliance departments across various industries, including healthcare and finance
Employer & Industry UsageUsed in regulated industries to prepare and submit regulatory documentsUsed to ensure company adherence to laws and regulations, often involving audits and policy development

The Regulatory Associate primarily focuses on preparing and managing regulatory submissions within life sciences industries, while the Compliance Specialist ensures ongoing adherence to laws and regulations across various sectors. Both roles require similar educational backgrounds and certifications, but their core responsibilities and work environments differ slightly, with Regulatory Associates working more directly with regulatory agencies and Compliance Specialists focusing on internal compliance processes.

More about Regulatory Associate jobs
What are the most commonly searched types of Regulatory jobs in Silver Spring, MD? The most popular types of Regulatory jobs in Silver Spring, MD are:
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What job categories do people searching Regulatory Associate jobs in Silver Spring, MD look for? The top searched job categories for Regulatory Associate jobs in Silver Spring, MD are:
What cities near Silver Spring, MD are hiring for Regulatory Associate jobs? Cities near Silver Spring, MD with the most Regulatory Associate job openings:
Regulatory Associate jobs near you
Infographic showing various Regulatory Associate job openings in Silver Spring, MD as of May 2026, with employment types broken down into 2% As Needed, 84% Full Time, 10% Part Time, and 4% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $69,043 per year, or $33.2 per hour.

Associate - Healthcare Regulatory Compliance

Advocates Legal Recruiting

Washington, DC • Hybrid

$260K - $365K/yr

Full-time

Medical, Dental, Vision, Retirement

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

Job description

Healthcare Regulatory Associate

Healthcare Regulatory Associate (3–5 YOE) Hybrid | Washington, D.C. (preferred), NYC, or Chicago Join a Healthcare Law Dream Team One of the most respected names in BigLaw (yep, you know them—but we're keeping it low-key) is on the hunt for a sharp, curious, and purpose-driven Healthcare Regulatory Associate to dive into some of the most complex and forward-thinking work in the healthcare and life sciences world. If you're 3–5 years into your legal journey, love decoding the intersection of health tech, regulation, and M&A, and want to be in the room where it happens—this gig's for you. The Vibe This team is where law meets innovation. Think: Advising digital health disruptors and next-gen telehealth companies Navigating regulatory mazes like HIPAA, Anti-Kickback, Stark, and licensing Getting hands-on with deal structuring, private equity transactions, and compliance builds Zooming out to shape strategy with clients, not just push paper You'll work closely with folks who've been at CMS, DOJ, FDA—aka, people who know their stuff and want to help you level up. Your Toolkit 3–5 years of real-deal healthcare regulatory experience Exposure to M&A or investment work? Gold star. Agency-side chops (CMS/OCR/DOJ/FDA)? Big plus. JD in hand + bar admission in DC, IL, or NY Clear thinker. Strong writer. Deeply organized. Inherently collaborative. Why You'll Love It Here $260K–$365K salary (no gatekeeping) Hybrid setup = flexibility meets community You'll join a firm that actually invests in its people (and not just during onboarding) Full-on benefits: health, vision, dental, 401(k), and the soft stuff like mentorship, real feedback, and opportunities to lead If you're looking to make bold moves in healthcare law and want your next chapter to be equal parts impactful and inspiring—this is it. Slide into our DMs (or click I'm Interested) Apply through the link or reach out if you want to chat before making moves.

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