FDA Attorney
Pine Brook, NJ · On-site +1
In the Life Sciences, Firm X, has represented pharmacies of all kinds and assisted with regulatory ... fully remote office. They receive an average of 5 new FDA client inquiries per week.
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FDA Attorney
Pine Brook, NJ · On-site +1
In the Life Sciences, Firm X, has represented pharmacies of all kinds and assisted with regulatory ... fully remote office. They receive an average of 5 new FDA client inquiries per week.
Senior FDA Attorney
Pine Brook, NJ · On-site +1
$250K - $400K/yr
... Remote A nationally recognized boutique law firm focused exclusively on healthcare and life sciences is seeking an experienced FDA Attorney to join its growing regulatory practice. This is a senior ...
Senior FDA Attorney
Pine Brook, NJ · On-site +1
$250K - $400K/yr
... Remote A nationally recognized boutique law firm focused exclusively on healthcare and life sciences is seeking an experienced FDA Attorney to join its growing regulatory practice. This is a senior ...
Medical Editor
Washington, DC · Remote
Currently 100% remote. Please be aware that the workplace type allowed is approved by the client ... The Medical Editor will format and proofread documents written by FDA scientists, format data ...
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Medical Editor
Washington, DC · Remote
Currently 100% remote. Please be aware that the workplace type allowed is approved by the client ... The Medical Editor will format and proofread documents written by FDA scientists, format data ...
Medical Editor
Washington, DC · Remote
Currently 100% remote. Please be aware that the workplace type allowed is approved by the client ... The Medical Editor will format and proofread documents written by FDA scientists, format data ...
Medical Editor
Washington, DC · Remote
Currently 100% remote. Please be aware that the workplace type allowed is approved by the client ... The Medical Editor will format and proofread documents written by FDA scientists, format data ...
... life sciences organization. The consultant will serve as a key regulatory advisor, providing ... Review NDA content for completeness, consistency, compliance risks, and FDA readiness. * Identify ...
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... life sciences organization. The consultant will serve as a key regulatory advisor, providing ... Review NDA content for completeness, consistency, compliance risks, and FDA readiness. * Identify ...
... FDA regulatory reviewers and scientific personnel. This position is contingent upon award. Work Schedule and Location * This position is remote with periodic on-site presence at Silver Spring, MD
... FDA regulatory reviewers and scientific personnel. This position is contingent upon award. Work Schedule and Location * This position is remote with periodic on-site presence at Silver Spring, MD
Principal, Clinical Scientist Valencia, California - Hybrid preferred | REMOTE FOR THE RIGHT ... Strong knowledge of ICH-GCP, ISO 14155, FDA regulations, and medical device clinical development.
Principal, Clinical Scientist Valencia, California - Hybrid preferred | REMOTE FOR THE RIGHT ... Strong knowledge of ICH-GCP, ISO 14155, FDA regulations, and medical device clinical development.
Scientist II
College Park, MD · Remote
Role: Scientist II Location: (Remote but need to report to the duty station in college park, MD or other FDA facilities within DC metropolitan area as per need) : So, look for local candidates.
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Scientist II
College Park, MD · Remote
Role: Scientist II Location: (Remote but need to report to the duty station in college park, MD or other FDA facilities within DC metropolitan area as per need) : So, look for local candidates.
Biocompatibility Scientist
FL · Remote
$145 - $150/hr
Remote (Client HQ: Gainesville, FL - No relocation required) Job Summary We are seeking an ... Ensure compliance with applicable Quality Systems , FDA regulations, and international biological ...
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Biocompatibility Scientist
FL · Remote
$145 - $150/hr
Remote (Client HQ: Gainesville, FL - No relocation required) Job Summary We are seeking an ... Ensure compliance with applicable Quality Systems , FDA regulations, and international biological ...
Remote / Watsonville, CA Salary - 103K - 120K Regulatory Claims Substantiation Scientist Job ... Stay abreast of the latest dietary supplement risks from FDA, FTC, and third-party litigation.
Remote / Watsonville, CA Salary - 103K - 120K Regulatory Claims Substantiation Scientist Job ... Stay abreast of the latest dietary supplement risks from FDA, FTC, and third-party litigation.
Principal Clinical Scientist
Atlanta, GA · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Atlanta, GA · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Los Angeles, CA · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Los Angeles, CA · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Miami, FL · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Miami, FL · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Raleigh, NC · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Raleigh, NC · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Detroit, MI · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Detroit, MI · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Chaska, MN · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Chaska, MN · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Cleveland, OH · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Cleveland, OH · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Charlotte, NC · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Charlotte, NC · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Salt Lake City, UT · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Salt Lake City, UT · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Tulsa, OK · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Principal Clinical Scientist
Tulsa, OK · On-site +1
... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...
Remote Fda Scientist information
See salary details
$83.5K - $91.5K
5% of jobs
$91.5K - $99.4K
6% of jobs
$99.4K - $107.4K
12% of jobs
$108.6K is the 25th percentile. Wages below this are outliers.
$107.4K - $115.3K
12% of jobs
$115.3K - $123.3K
14% of jobs
The median wage is $124.1K / yr.
$123.3K - $131.2K
15% of jobs
$131.2K - $139.2K
11% of jobs
$140.2K is the 75th percentile. Wages above this are outliers.
$139.2K - $147.1K
11% of jobs
$147.1K - $155.1K
7% of jobs
$155.1K - $163K
4% of jobs
$163K - $171K
4% of jobs
$83.5K
$127K
$171K
How much do remote fda scientist jobs pay per year?
As of Sep 7, 2026, the average yearly pay for remote fda scientist in the United States is $127,031.00, according to ZipRecruiter salary data. Most workers in this role earn between $109,000.00 and $143,500.00 per year, depending on experience, location, and employer.
What is a remote FDA scientist?
A Remote FDA Scientist is a professional who works for or with the U.S. Food and Drug Administration (FDA) from a remote location, rather than onsite at an FDA facility. These scientists are involved in a variety of regulatory, research, and review activities related to food, drugs, medical devices, or other products overseen by the FDA. Their responsibilities may include evaluating scientific data, reviewing submissions from manufacturers, and ensuring products meet safety and efficacy standards. Remote FDA Scientists typically collaborate with colleagues and stakeholders through virtual communication tools while maintaining strict compliance with federal guidelines.
What are the key skills and qualifications needed to thrive as a remote FDA scientist?
To thrive as a Remote FDA Scientist, you need a strong background in life sciences or a related field, advanced analytical skills, and experience with regulatory compliance, often supported by a relevant degree (such as a PhD or MS) and prior FDA or industry experience. Familiarity with data analysis tools, regulatory submission systems (like eCTD), and quality management software is typical. Excellent written communication, attention to detail, and the ability to work independently are vital soft skills in this role. These competencies ensure accurate scientific evaluation, effective regulatory submissions, and compliance with FDA standards while working remotely.
What are some common challenges faced by remote FDA scientists in maintaining effective communication with regulatory teams?
Remote FDA Scientists often navigate the challenge of ensuring clear and timely communication with cross-functional regulatory teams, especially when working across different time zones. This role requires proactive use of collaboration tools, regular virtual meetings, and detailed documentation to keep everyone aligned on project goals and compliance requirements. Building strong relationships with colleagues and setting clear expectations for updates and feedback can help mitigate miscommunication and support project success. Additionally, staying organized and being responsive to regulatory changes are key to thriving in a remote environment.
What is the difference between Remote Fda Scientist vs Remote Fda Reviewer?
| Aspect | Remote Fda Scientist | Remote Fda Reviewer |
|---|---|---|
| Required Credentials | Advanced degree in life sciences, relevant certifications | Similar credentials, often with additional regulatory training |
| Work Environment | Research labs, regulatory agencies, or remote settings | Primarily review submissions remotely, office or home-based |
| Industry Usage | Research, development, and regulatory compliance | Reviewing and approving drug, device, or food applications |
| Common Search Intent | Understanding roles, qualifications, and remote opportunities | Differences in responsibilities, qualifications, and remote work |
Remote Fda Scientists focus on research and development activities, while Remote Fda Reviewers primarily evaluate submissions for approval. Both roles require similar scientific credentials and often operate remotely within the regulatory industry. The main difference lies in their core responsibilities: scientists conduct research, whereas reviewers assess regulatory submissions.
More about Remote Fda Scientist jobs
What cities are hiring for Remote Fda Scientist jobs?
Cities with the most Remote Fda Scientist job openings:
What are the most commonly searched types of Fda Scientist jobs?
The most popular types of Fda Scientist jobs are:
What states have the most Remote Fda Scientist jobs?
States with the most job openings for Remote Fda Scientist jobs include:
What job categories do people searching Remote Fda Scientist jobs look for?
The top searched job categories for Remote Fda Scientist jobs are:
Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 16 days ago
Job description
TITLE: FDA ATTORNEY POSITIION: DIRECT HIRE Firm X, established in 2000, is a national boutique law firm focused exclusively on Healthcare and Life Sciences. The Firm draws on its experience representing stakeholders across the entire healthcare spectrum. In the Life Sciences, Firm X, has represented pharmacies of all kinds and assisted with regulatory, transactional, and litigation matters. On the Healthcare side, the Firm's clients have included large physician group practices, hospitals, hospital medical staff, ambulatory surgery centers, laboratory companies, as well as the complete panoply of ancillary service providers. Firm X attorneys are licensed in numerous states. The Firm has offices in Pine Brook, New Jersey, and New York City. A Mid-Level or more senior FDA Attorney (Counsel-level or higher) is sought for Firm X’s Pine Brook, NJ, New York City, or fully remote office. They receive an average of 5 new FDA client inquiries per week. Responsibilities will align with the Attorney’s background, which should include: • Compounding rules, regulations and FDA guidance o 503A o 503B o Bulk API suppliers and repackagers o FDA audits/investigations • Drug supply chain security and track and trace o Trading partner requirements o Unique trading partners (i.e., 3PLs, brokers, etc.) o Serialization implementation requirements o Other drug supply chain considerations • Drug and device manufacturing rules o CGMP compliance o NDA and ANDA filings and evaluation o 510K Premarket Approval Filings and evaluation o OTC filings and evaluation o Advice on manufacturing practices • Clinical trial rules o Structuring and drafting clinical trial agreements, informed consent forms, master service agreements, and related research contracts o Institutional Review Board (IRB) submissions and compliance o Clinical trial design, study initiation, data use, adverse event reporting, and post-trial obligations • Labeling and advertising reviews • FDA registration and annual filings • FDA inspections, 483 responses and warning letters • Drug withdrawals and recalls • FDA importation and exportation rules • Veterinary medicine and veterinary compounding • Dietary supplements • FDA regulated medical devices • Reviews of clinical literature and incorporation into arguments/strategies (access to these clinical literature directories is a plus) Requirements: • 10+ years FDA experience – private law firm experience strongly preferred, but will also consider in-house candidates • Clinical trial experience a plus • Filing copyrights a plus • Filing patents a plus • May work in the Pine Brook or New York City office; will also consider fully remote arrangement if located in other states • Admitted to practice in at least one US state • Experience performing most/all of the job responsibilities of the position (outlined above) • Team-player mindset, and ability to work cohesively and collaboratively with a team of attorneys • Strong work ethic Benefits: Firm X offers a hybrid schedule, competitive salary, and a full range of benefits, including PTO, medical, dental, vision, 401(k) (upon eligibility to participate), on-site gym (Pine Brook), and opportunities for substantial salary progression based on performance and contributions. *The posted salary will depend on years of experience and other factors.