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Regulatory Science Jobs in Reston, VA (NOW HIRING)

Brillient

Data Scientist

Silver Spring, MD

... regulatory science. The employee should have significant expertise in data science. Specific tasks shall include, but not be limited to, the following: * * Reviews and evaluate clinical study ...

IMAGINEEER LLC

Scientific Data Analyst

Arlington, VA · On-site

$110K - $115K/yr

This role sits at the intersection of data science, regulatory science, and biomedical research. Key Responsibilities: * Develop and execute analytical workflows to process, analyze, and interpret ...

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Regulatory Science information

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$52

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How much do regulatory science jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for regulatory science in Reston, VA is $52.18, according to ZipRecruiter salary data. Most workers in this role earn between $36.35 and $54.13 per hour, depending on experience, location, and employer.

What is a Regulatory Science job?

A Regulatory Science job involves evaluating and developing scientific methods to assess the safety, efficacy, and quality of medical products, food, and other regulated items. Professionals in this field work at the intersection of science, policy, and regulation to ensure compliance with government standards. They may collaborate with regulatory agencies, industry stakeholders, and researchers to facilitate product approvals and post-market surveillance.

What can you do with a regulatory science degree?

A regulatory science degree prepares individuals for roles in regulatory affairs, compliance, and policy within industries such as pharmaceuticals, biotechnology, and medical devices. Graduates can work as regulatory specialists, managers, or consultants, ensuring products meet legal and safety standards, often using knowledge of regulations, documentation, and scientific principles.

What are the key skills and qualifications needed to thrive in the Regulatory Science position, and why are they important?

To thrive in Regulatory Science, you need a solid background in life sciences or a related field, strong analytical and research skills, and familiarity with regulatory frameworks. Experience with regulatory submission systems (like eCTD), knowledge of global regulations, and certifications such as RAC (Regulatory Affairs Certification) can be highly advantageous. Excellent attention to detail, problem-solving abilities, and strong cross-functional communication are critical for success in this field. These competencies ensure regulatory compliance and efficient product development while minimizing delays and risks for organizations bringing products to market.

Is regulatory a good career?

Regulatory science is a growing field that involves ensuring products like pharmaceuticals, medical devices, and food meet safety and compliance standards. It offers opportunities in industries such as healthcare, biotech, and government agencies, often requiring knowledge of regulations, good communication skills, and relevant certifications. The career can be stable and rewarding for those interested in public health and compliance roles.

What is the highest paying job in regulatory affairs?

The highest paying roles in regulatory affairs are typically senior executive positions such as Vice President or Director of Regulatory Affairs, which can earn six-figure salaries. These roles often require extensive experience, advanced certifications, and leadership skills in managing regulatory strategies across global markets.

What does a regulatory scientist do?

A regulatory scientist evaluates and ensures that products such as pharmaceuticals, medical devices, or food meet government regulations and safety standards. They analyze data, prepare documentation for regulatory submissions, and stay updated on evolving policies, often using tools like compliance databases and scientific research methods.

What are the typical responsibilities of a Regulatory Science professional in the workplace?

Regulatory Science professionals are responsible for ensuring that products comply with regulations throughout all development and commercialization stages. Their daily activities may include preparing and submitting regulatory documents, collaborating with R&D, quality assurance, and legal teams, and interpreting updates to regulations or guidelines that affect product approval. They may also interact directly with regulatory agencies and participate in strategic meetings to help guide product development decisions. Working in Regulatory Science often means being a key liaison between internal teams and regulatory authorities to facilitate smooth approvals and ongoing compliance.

What job categories do people searching Regulatory Science jobs in Reston, VA look for? The top searched job categories for Regulatory Science jobs in Reston, VA are:
What cities near Reston, VA are hiring for Regulatory Science jobs? Cities near Reston, VA with the most Regulatory Science job openings:
Regulatory Science jobs near you
Infographic showing various Regulatory Science job openings in Reston, VA as of July 2026, with employment types broken down into 1% As Needed, 86% Full Time, 10% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $108,527 per year, or $52.2 per hour.
Director, New Approach Methodologies

Director, New Approach Methodologies

Foundation for the NIH

North Bethesda, MD • On-site

$185K - $225K/yr

Other

Posted 3 days ago

New

Job description

Director, New Approach Methodologies
North Bethesda, MD 20852
Position Type: Full Time
Salary Range: $185,000.00 - $225,000.00 Salary/year
Description

The Foundation for the National Institute of Health (FNIH) is seeking a Director, New Approach Methodologies (NAMs) for toxicology and drug development, who will lead the strategy, development, and execution of multi-sector scientific partnerships to advance, validate, and qualify innovative alternative models for drug development and human safety toxicity testing. These efforts will be under the banner of the NAMs Validation and Qualification Network (VQN) that is currently being stood up as a pillar to the Complement Animal Research in Experimentation (Complement-ARIE) Consortium facilitated by the National Institutes of Health (NIH). The projects within the VQN will include all types of NAMs, including in silico approaches, in vitro (e.g. microphysiological systems (MPS), organoids, and advanced cell/tissue systems), in chemico, and ex vivo, and the goal will be to drive these NAMs to a state of readiness for acceptance by the appropriate regulatory body.


This role sits at the intersection of translational science, regulatory science, and collaborative innovation. The Director will work closely with biopharmaceutical, chemical, agrichemical, and comestics companies, regulatory agencies, academic investigators, and patient-focused organizations to accelerate the adoption of scientifically robust, fit-for-purpose models that improve predictive safety assessment and drug development and reduce reliance on traditional animal testing. This position will report to the Senior Vice President of Translational Science within the Science Partnerships department and is based at the FNIH offices located in North Bethesda, MD.


The ideal candidate brings deep expertise in preclinical drug development and toxicology, paired with the ability to lead complex, precompetitive collaborations, and design projects that will move toward regulatory acceptance.


Key Responsibilities


Scientific & Program Leadership & Portfolio Management


  • Develop and lead a strategic portfolio of programs focused on NAMs for drug development and human safety/toxicity assessment


  • Identify high-impact use cases where NAMs can be developed precompetitively for validation and qualification for regulatory agencies, including FDA, EMA, EPA, and others in the US and globally


  • Facilitate group creation of scientific frameworks for model validation, context of use (COU) definition, and evidentiary standards


  • Design, launch, and manage multi-partner collaborations across industry, academia, government, and nonprofits


  • Build trusted relationships with biopharma, chemical, agrichemical, and cosmetics R&D leaders, regulatory scientists, and academic innovators


    • Regulatory Science & Qualification Pathways


  • Lead efforts to align validation strategies with regulatory expectations (e.g., FDA, EMA, PMDA, EPS, OECD, etc.)


  • Translate emerging science into regulatory-ready, validated models for submission to the relevant qualification programs (e.g., iSTAND, ENTRÉE, OECD, etc.)


    • Program Oversight & Delivery


  • Ensure rigorous governance of all of the VQN and each precompetitive project developed


  • Aid the VQN project leads on milestone tracking and financial stewardship


  • Lead cross-functional workstreams including internal staff and external partners to address key needs in the NAMs validation and qualification space


    • Field Building & Thought Leadership


  • Represent the organization in scientific and policy forums and partner interactions


  • Contribute to publications and consensus frameworks that advance the field


    • Required


  • PhD or equivalent in toxicology, pharmacology, biomedical sciences, or related field


  • 10+ years of experience in biopharmaceutical R&D, regulatory science, or translational research


  • Demonstrated expertise in preclinical drug development and safety assessment


  • Experience with NAMs (e.g., in silico, in vitro, in chemico, ex vivo)


  • Proven ability to lead complex, cross-institutional scientific collaborations


    • Preferred


  • Direct experience interacting with regulatory agencies or contributing to regulatory submissions, including either drug development or environmental regulation


  • Experience with NAM validation and/or qualification for regulatory acceptance


  • Familiarity with global regulatory frameworks and emerging NAM guidance


  • Strong track record of scientific team leadership


    • This is a hybrid position and requires regular visits to FNIH headquarters in Bethesda, MD. This position may also require occasional travel for meetings, conferences and any other relevant engagements.


    At FNIH we are committed to living our core values every day. If you are excited about this role and the work of the Foundation, but your experience doesn’t align perfectly with all the qualifications in the job description, we encourage you to apply nonetheless. You may be just the right candidate for this or other roles at FNIH.


    Compensation details: 185000-225000 Yearly Salary


    PI07eb2b81c350-37820-40192606

    Apply