ZipRecruiter

Log In

2

Remote Fda Jobs in Washington (NOW HIRING)

Kaiva Corp

Epidemiologist

Washington, DC · Remote

Currently 100% remote. Please be aware that the workplace type allowed is approved by the client ... Desired Experience and Skills: · Experience supporting FDA, CDC, NIH, or other federal public ...

Kaiva Tech

Epidemiologist

Washington, DC · On-site +1

Currently 100% remote. Please be aware that the workplace type allowed is approved by the client ... Desired Experience and Skills : · Experience supporting FDA, CDC, NIH, or other federal public ...

Team Carney

Program Manager

Silver Spring, MD · On-site +1

Food and Drug Administration (FDA). This position is contingent upon award. This position is remote with periodic on-site presence at Silver Spring, MD. Clearance Requirement: Current or ability to ...

Booz Allen Hamilton, Inc.

IT Project Manager

Bethesda, MD · On-site +1

$99K - $225K/yr

Remote Work: No Job Number: R0248458 Location: Bethesda,MD,US Share job via: Share IT Project ... Knowledge of applications that support the FDA's Office of Inspections and Investigations * PMP ...

micro1 AI

Director of Biostatistics

Washington, DC · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

micro1 AI

Biostatistician

Alexandria, VA · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

micro1 AI

Compliance Officers

Washington, DC · Remote

$50 - $80/hr

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project ... FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to critically read clinical or safety ...

micro1 AI

Regulatory Affairs Specialist

Alexandria, VA · Remote

$50 - $80/hr

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project ... FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to critically read clinical or safety ...

micro1 AI

Regulatory Affairs Specialist

Washington, DC · Remote

$50 - $80/hr

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project ... FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to critically read clinical or safety ...

micro1 AI

Compliance Officers

Alexandria, VA · Remote

$50 - $80/hr

Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project ... FDA, EMA, MHRA, PMDA, or Health Canada). * Proven ability to critically read clinical or safety ...

micro1 AI

Biostatistician

Washington, DC · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

micro1 AI

Director of Biostatistics

Alexandria, VA · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

WearLinq

Medical Billing Associate

Rockville, MD · On-site +1

$44K/yr

Wearlinq is reimagining ambulatory cardiac monitoring with the first FDA-cleared, real-time, six ... Benefits: * Optional Remote work opportunity * 401(k) * Dental insurance * Health insurance

previous pagenext page

Showing results 21-40

All JobsFda JobsRemote Fda JobsRemote Fda Jobs in Washington

Remote Fda information

See Washington salary details

$27.9K

$95.2K

$187.4K

How much do remote fda jobs pay per year?

As of Sep 9, 2026, the average yearly pay for remote fda in Washington is $95,172.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,293.00 and $123,471.00 per year, depending on experience, location, and employer.

What is a remote FDA?

A Remote FDA job typically involves working for or with the U.S. Food and Drug Administration (FDA) from a remote location. These roles can include regulatory affairs, compliance, medical writing, research, and reviewing submissions for drug and medical device approvals. Remote FDA jobs require knowledge of FDA regulations, strong analytical skills, and experience in healthcare, pharmaceuticals, or related fields. They offer flexibility while maintaining high regulatory standards and ensuring public health and safety.

What are the typical daily responsibilities of a remote FDA compliance specialist?

A Remote FDA Compliance Specialist generally reviews and updates regulatory documents, conducts virtual audits, and monitors company practices for FDA compliance. They regularly collaborate with cross-functional teams, such as quality assurance, legal, and product development, to provide guidance on regulatory requirements and respond to compliance queries. Additionally, they prepare and submit necessary reports, maintain records for inspections, and stay current on evolving regulations. This remote structure allows flexibility but also demands excellent organization, communication, and self-discipline to ensure all deadlines and compliance standards are met.

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

To excel as a Remote FDA Compliance Specialist, you need in-depth knowledge of FDA regulations, quality assurance procedures, and a background in life sciences or a related field. Proficiency in using compliance management systems, electronic document management tools, and relevant certifications such as RAC (Regulatory Affairs Certification) are often required. Exceptional attention to detail, self-motivation, and strong written and verbal communication skills are vital for remote collaboration and thorough documentation. These abilities ensure regulatory adherence, minimize compliance risks, and facilitate effective remote teamwork within the pharmaceutical or medical device industry.

What jobs can I do completely remotely as a remote FDA?

A remote FDA typically refers to a Food and Drug Administration-related role that can be performed remotely, such as regulatory affairs specialists, quality assurance managers, or compliance analysts. These positions often require knowledge of regulations, strong communication skills, and familiarity with digital tools for document review and reporting, allowing work to be done entirely online. However, some roles may require occasional on-site visits or inspections depending on the specific job and employer policies.

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

The most popular types of Fda jobs in Washington are:

What are popular job titles related to Remote Fda jobs in Washington?

For Remote Fda jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Remote Fda jobs in Washington look for?

The top searched job categories for Remote Fda jobs in Washington are:

What cities in Washington are hiring for Remote Fda jobs?

Cities in Washington with the most Remote Fda job openings:

Remote Fda jobs near you
Infographic showing various Remote Fda job openings in Washington as of September 2026, with employment types broken down into 84% Full Time, 8% Part Time, and 8% Contract. Highlights an 100% Remote job distribution, with an average salary of $95,172 per year, or $45.8 per hour.

Epidemiologist

Washington, DC • Remote

Kaiva Corp
See more jobs at Kaiva Corpexternal

Full-time

Posted 13 days ago

Job description

Kaiva Tech, LLC is seeking an Epidemiologist in the DC Metro Area. Clearance: Ability to obtain a Public Trust Workplace Type: Currently 100% remote. Please be aware that the workplace type allowed is approved by the client and is subject to change dependent on client needs and expectations. Summary Overview:The Subject Matter Expert (Mid)–Epidemiologist provides scientific, epidemiologic, and technical support to government staff responsible for the review of vaccines and related biological products. The contractor supports regulatory review activities by assisting in the evaluation and interpretation of epidemiologic data, preparation of scientific and regulatory documents, development of briefing materials, and communication of complex scientific information to a variety of audiences. Working closely with government stakeholders, the Epidemiologist contributes to the preparation of product reviews, advisory committee briefing documents, scientific publications, presentations, and responses to information requests. The position requires extensive experience in pharmacoepidemiology, strong scientific writing skills, and the ability to support time-sensitive regulatory reviews while ensuring compliance with applicable laws, regulations, policies, and review procedures governing vaccines and biological products. Supervisory Responsibilities:· None. Essential Duties and Responsibilities:As a Subject Matter Expert (Mid)–Epidemiologist, your responsibilities will include, but are not limited to the following: · Support government staff in the review and evaluation of regulatory submissions for vaccines and related biological products, including BLAs, EUAs, supplements, and other regulatory applications.· Develop and maintain knowledge of FDA review processes, scientific standards, and regulatory requirements applicable to vaccines and biological products.· Assist in the preparation, editing, and quality review of regulatory and scientific documents, including review memoranda, advisory committee briefing materials, technical reports, regulatory summaries, and responses to information requests.· Review, interpret, and evaluate epidemiologic data from healthcare claims databases, electronic health records, registries, surveillance systems, and other real-world data sources.· Assess study designs, methodologies, and analytical approaches; identify data gaps and recommend additional analyses to support regulatory decision-making.· Synthesize complex scientific, epidemiologic, and public health information into clear, accurate, and actionable conclusions for technical and non-technical audiences.· Support the development of scientific manuscripts, study protocols, white papers, presentations, and submissions to peer-reviewed journals.· Develop and maintain visual communication products, including graphs, tables, figures, and infographics, to effectively communicate scientific findings and regulatory information.· Collaborate with government stakeholders to prioritize assignments, coordinate deliverables, and support time-sensitive regulatory reviews.· Apply project management principles to manage multiple concurrent assignments, monitor progress, and ensure timely completion of deliverables.· Ensure all work products comply with applicable federal laws, regulations, agency policies, quality standards, and Section 508 accessibility requirements.· Maintain confidentiality and adhere to established FDA templates, documentation practices, and review procedures. Required Experience and Skills:· Minimum of seven (7) years of experience conducting pharmacoepidemiology studies using large healthcare claims databases, electronic health record systems, or comparable real-world data sources.· Demonstrated experience supporting scientific research, regulatory review activities, or public health programs involving drugs, vaccines, or biological products.· Experience synthesizing and communicating complex scientific, regulatory, policy, or public health information to diverse audiences.· Experience managing multiple time-sensitive projects and coordinating activities across stakeholders. Desired Experience and Skills:· Experience supporting FDA, CDC, NIH, or other federal public health agencies.· Experience with vaccine safety, vaccine effectiveness, or biological product surveillance studies.· Knowledge of regulatory science principles and risk-benefit assessment methodologies.· Publication record in peer-reviewed scientific journals.· Experience preparing scientific briefing materials for advisory committees, executive leadership, or regulatory decision makers. Education:· Post-Doctoral Degree in Epidemiology, Pharmacoepidemiology, Public Health, Biostatistics, Medicine, Pharmacy, Health Outcomes Research, or a closely related scientific discipline. Certificates, Licenses and Registrations:· None. Physical Requirements:· Ability to sit and work with a computer for prolonged periods of time.
Job Posted by ApplicantPro