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Live In Fda Scientist Jobs in Virginia (NOW HIRING)

Noblis

Principal Regulatory Scientist

Reston, VA · On-site

The Principal Regulatory Scientist will work closely with client program managers, product ... Experience with FDA's Animal Rule and development programs in which human efficacy studies are ...

3 Media Web Solutions, Inc

Data Scientist II

Arlington, VA · On-site

$107.30 - $124.20/hr

Position Overview Data Scientist II - partner with Product, Marketing, and Finance stakeholders to ... S., we will prioritize those who live in the Washington‑Baltimore metropolitan area and who are ...

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All JobsLive In Fda Scientist JobsLive In Fda Scientist Jobs in Virginia

Live In Fda Scientist information

What is a live in FDA scientist?

A Live In FDA Scientist typically refers to a regulatory scientist who works for the U.S. Food and Drug Administration (FDA) and may be involved in on-site or continuous monitoring of studies, often in clinical or laboratory settings. Their role includes evaluating scientific data, ensuring compliance with federal regulations, and overseeing the safety and efficacy of products such as drugs, biologics, or medical devices. Live-in positions might be required for research facilities needing 24/7 oversight, although such roles are rare and specialized. These scientists play a crucial role in public health by supporting the FDA’s mission to protect consumers.

What are some unique challenges faced by a live in FDA scientist, and how can they be managed?

A Live-In FDA Scientist often works in environments such as research facilities or clinical trial sites where on-site presence is essential. This setup can present challenges like maintaining work-life balance, adapting to extended hours, and managing confidentiality due to the sensitive nature of ongoing research. Successful candidates typically develop strong time management skills, set clear personal boundaries, and foster open communication with team members to ensure both professional responsibilities and personal well-being are balanced. Collaboration with multidisciplinary teams is frequent, and adaptability is key to thriving in this dynamic role.

What are the key skills and qualifications needed to thrive as a live in FDA scientist, and why are they important?

To thrive as an FDA Scientist, you need a strong background in life sciences or chemistry, typically with an advanced degree (MS or PhD) and experience in research or regulatory affairs. Familiarity with laboratory instrumentation, data analysis software, and FDA regulatory systems is essential, and certifications like RAC (Regulatory Affairs Certification) can be advantageous. Attention to detail, critical thinking, and excellent communication skills help you interpret data accurately and collaborate effectively with multidisciplinary teams. These skills ensure scientific integrity, regulatory compliance, and the advancement of public health through safe and effective products.

What is the difference between Live In Fda Scientist vs Fda Reviewer?

AspectLive In Fda ScientistFda Reviewer
Required credentialsBachelor's or Master's in Life Sciences, relevant experienceSimilar credentials, often with advanced degrees
Work environmentOn-site, often in government or research facilitiesOffice-based, reviewing submissions at FDA headquarters or regional offices
Employer and industry usageFederal government, regulatory scienceFederal government, regulatory review
Common search intentJob duties, qualifications, work conditionsComparison of roles, responsibilities, career path

The Live In Fda Scientist and Fda Reviewer roles both require scientific expertise and federal employment credentials. While the Live In Fda Scientist often involves conducting research and scientific analysis on-site, the Fda Reviewer primarily focuses on evaluating regulatory submissions and documentation. Both roles are integral to FDA operations, but they differ in daily tasks and work environment, with the scientist more research-oriented and the reviewer more review-focused.

How much do live in FDA scientists make?

Live-in FDA scientists typically earn a salary comparable to federal scientific positions, which can range from approximately $70,000 to over $130,000 annually depending on experience, education, and location. They often receive benefits such as health insurance and retirement plans, and may work in regulated environments requiring specialized certifications.

What are the most commonly searched types of Fda Scientist jobs in Virginia?

The most popular types of Fda Scientist jobs in Virginia are:

What cities in Virginia are hiring for Live In Fda Scientist jobs?

Cities in Virginia with the most Live In Fda Scientist job openings:

Live In Fda Scientist jobs near you

Senior Research Analyst, Quality and Compliance (Pharmaceutical, Biotech)

Politico

Arlington, VA • On-site

$133K - $134K/yr

Full-time

Re-posted 28 days ago

Job description

Job Description:
POLITICO is seeking a Senior Research Analyst to help lead part of its regulatory intelligence and information services product, AgencyIQ. Since its founding in early 2020, AgencyIQ has quickly become the premier source of regulatory intelligence and analysis for professionals working in the life sciences, foods and chemicals industries.
Our written research and analysis are relied upon by many top companies, trade groups, law firms and advocacy groups to help them understand breaking news, identify emerging trends, predict future action and prepare for seismic shifts in regulatory policy.
As a subject matter specialist in the regulation of drug product quality (including pharmaceuticals, biopharmaceuticals and biotechnology products) and compliance topics related tothe U.S. Food and Drug Administration (FDA) and other key global regulators, the Senior Research Analyst will be responsible for analyzing the relevance of regulatory changes and developments, tracking and identifying trends in FDA compliance on regulated products, articulating the type and degree of impact on industry, and providing context to an audience of knowledgeable regulatory professionals.
Reporting to the Senior Director for Life Sciences Research in POLITICO's Arlington, Virginia offices, the Senior Research Analyst will join a team of experienced researchers responsible for producing a mix of daily written content, in-depth written research, weekly insights, directed deliverables and presentations.
Expected areas of subject matter coverage will include regulations, guidance, international standards, legislation, announcements, FDA enforcement and compliance trends, and current good manufacturing practice-related developments.
What You'll Do
  • Produce daily (3-4 per week) topical intelligence articles and other content for our subscribers based on emerging regulatory and legislative developments related to the FDA's regulation of drug quality and other closely related topics

  • Serve as a subject matter specialist on matters of drug quality and compliance

  • Lead or participate in the development and delivery of in-depth analysis, deep-dive research, webinars and email newsletters

  • Participate in subscriber- and prospect-facing events, and briefings

What you'll need
  • At least 3 years' experience analyzing FDA regulatory policies at a consulting company, think tank, trade association, government agency, life sciences company, or media outlet with an emphasis on quality regulations

  • An affinity for writing - efficiently and effectively, and for a business or policy audience - paired with a knowledge of (and passion for) regulation and regulatory policy

  • Experience and comfort working in fast-paced, research-driven environments in which daily delivery of written regulatory analyses is the norm

  • Experience with qualitative and quantitative analysis and trend tracking

  • A good working knowledge of FDA regulatory processes (and in particular those related to drugs and biotechnology products) and familiarity with FDA's compliance systems and databases; capable of delivering expert insights to our knowledgeable subscribers

While not required, you will stand out if you:
  • Have an advanced degree or certification related to the life sciences (i.e., a PhD, relevant master's degree, or J.D.)

  • Have prior experience working in media, including as a journalist or writing a product widely read by others (i.e., a business intelligence product or internal newsletter)

  • Have experience in quantitative analysis using FDA data sets

  • Experience presenting on regulatory topics to a variety of different audience types (small groups, large groups) in different environments (virtual and in-person)

At POLITICO, we value integrity, collaboration, and innovation. This role offers the opportunity to work alongside top executives and contribute to a dynamic HR team. If you are an organized, motivated, and detail-driven professional who thrives in an in-office setting, we encourage you to apply.
We value our people. Click here for more on what we offer and what it's like to work for POLITICO.
Let's keep in touch. You can view our list of open positions here and email us careers@politico.com. We hope to see your application soon!
About Us.
POLITICO illuminates the forces shaping global power. Since 2007, we have delivered intelligence that anticipates tomorrow's headlines, not reports on yesterday's news. As politics has increasingly become the defining force of our era, our work has never been more vital.
Cabinet secretaries and Ministers start their mornings with our analysis. CEOs shape strategy around our reporting. Advocacy leaders rely on our insights to move policy. We deliver the straightforward facts and clear-eyed analysis they need to navigate the most complex political landscape of our lifetimes.
Our 1,100+ publishing professionals across the world's key democratic capitals-Washington, Brussels, London, Paris, Berlin, Sacramento, and New York-form the world's premier politics and policy newsroom. We tell the story of how power really works by explaining who wields it and how they plan to exercise it, connecting dots others miss and delivering scoops from sources others don't even know exist.
Innovation has always been a core tenet of our story. At launch, we bet that depth would trump scale, that talent would trump traffic, and that politics would become central to modern life. In 2011, we made another bet and launched POLITICO Pro to help decision-makers understand the business of government, transforming both how they shape government action and the business of journalism itself.
These bets have made POLITICO the most successful digital news startup of its generation and the indispensable resource for leaders who shape the future. Today, we are a rarity in media: a growing, profitable, and sustainable news organization.
POLITICO is a subsidiary of Axel Springer SE, a family-owned transatlantic media company headquartered in Berlin and New York. Axel Springer is dedicated to shaping the future of journalism in the free world, believing that a free and informed society is essential to democracy. The company's guiding principles - first articulated as The Essentials by founder Axel Springer in the aftermath of World War II - remain a cornerstone of the company's foundation today. Learn more about Axel Springer
Posting date:
2026-03-31
Title:
Senior Research Analyst, Quality and Compliance (Pharmaceutical, Biotech)

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