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Regulatory Science Jobs in Reston, VA (NOW HIRING)

DCG

Social Scientist

Washington, DC · Remote

This position will contribute to the design, implementation, analysis, and reporting of qualitative and quantitative social science research projects focused on tobacco regulatory science and related ...

Brillient

Data Scientist

Silver Spring, MD · On-site

... 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 +1

$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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How much do regulatory science jobs pay per hour?

As of Jun 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 communication skills.

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.

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 scientific and regulatory knowledge to support product approval and compliance processes.

Which is better, RA or QA?

In regulatory science, RA (Regulatory Affairs) focuses on ensuring products comply with regulations and managing submissions to authorities, while QA (Quality Assurance) emphasizes maintaining product quality through testing and process controls. Both roles are essential and often collaborate; the choice depends on whether you prefer working with compliance documentation and regulations or quality systems and testing protocols.

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 June 2026, with employment types broken down into 1% As Needed, 75% Full Time, 21% 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.
Senior Regulatory Affairs Director (Infectious Diseases)

Senior Regulatory Affairs Director (Infectious Diseases)

AstraZeneca

Gaithersburg, MD • On-site

$211K - $317K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 71 rated pharmaceutical

Job description

AstraZeneca - Infectious Diseases
At AstraZeneca, we are committed to developing and delivering transformative vaccines and antibodies, providing long-lasting immunity for millions of people, where the burden of disease is greatest. During the COVID-19 pandemic, we played an important role as part of a truly global effort to respond to a new and unprecedented challenge. We will continue to advance science in infectious disease therapies and work with partners to drive improvements in public health and ensure our science reaches millions more people.
Role
The Senior Regulatory Affairs Director (SRAD) leads the global regulatory strategy for complex products. They aim to secure rapid approval that meets business, market, and patient needs. The SRAD offers strategic leadership and has expertise in global regulatory science, drug development processes, and strategies for high-profile programs. Familiarity with the disease area is essential to influence cross-functional discussions with Global Product Teams (GPT) and stakeholders. They can serve as the Global Regulatory Lead (GRL) for a product group and also act as a regional lead based on their location.
Your strategic leadership skills and deep understanding of global regulatory science from early to late-stage development into commercialisation strategy will be crucial in influencing cross-functional discussions and guiding high-profile development programs, as well as interacting with Global Health Authorities. Are you prepared to take on the Global Regulatory Lead role and drive innovative strategies for regulatory success?
Responsibilities
  • Effectively lead or deputise for Therapeutic Area (TA) VP/Regional VP in senior-level interactions internally or externally, including contributions to internal governance

  • Develop and implement regulatory strategies for products, ensuring rapid approval with advantageous labeling.

  • Lead the planning and construction of global dossiers and core prescribing information.

  • Conduct regulatory risk planning and mitigation.

  • Serve as the single point of contact and Global Regulatory Affairs representative on Product Development Teams.

  • Lead the Global Regulatory Sub-team to ensure regional regulatory needs are incorporated into the Global Regulatory Strategy and ensure execution on strategy.

  • Deliver all regulatory milestones, assess regulatory success probabilities, and implement risk mitigation measures.

  • Partner with marketing and regional regulatory affairs staff to help shape the environment and Health Authorities' views on relevant topics.

  • Lead regulatory staff on complex projects to ensure prioritized objectives are delivered on time and with quality.

  • Ensure effective regulatory representation at health authority meetings with clear documentation of discussions.

  • Lead the development and updates of the Regulatory Strategy Document for complex projects.

  • Monitor changes in the regulatory environment and advise Global Product Teams accordingly.

  • Provide regulatory leadership in product in-license/due diligence review, divestment, and withdrawal.

  • Lead complex projects designed to improve efficiencies and simplification, spanning cross functional areas.

Skills/Experience
  • Advanced degree in a science-related field and/or other appropriate knowledge/experience.

  • At least 10 years experience or equivalent of regulatory drug development including successful contribution to a major regulatory approval at a global level.

  • Experience in Infectious Diseases is strongly preferred.

  • Must have previous experience in leading Major Health Authority interactions (e.g., FDA advisory committee meetings, Oral explanations, Scientific Advice, Pre-NDA/BLA, EOP2 meetings etc.).

  • Proven leadership and program management experience, as well as the ability to think strategically and critically evaluate risks to regulatory activities.

  • Ability to work strategically within a complex, business-critical and high-profile development program.

Why AstraZeneca?
At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare.
Competitive salary and benefits package on offer:
Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week.
The annual base salary for this position ranges from $211,581.60 - 317,372.40. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles) or to receive a retirement contribution (hourly roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Date Posted
02-Jun-2026
Closing Date
27-Jun-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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