Medical Editor
Washington, DC ยท Remote
Currently 100% remote. Please be aware that the workplace type allowed is approved by the client ... The Medical Editor will support scientists at the US Food and Drug Administration (FDA) who ...
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Washington, DC ยท Remote
Currently 100% remote. Please be aware that the workplace type allowed is approved by the client ... The Medical Editor will support scientists at the US Food and Drug Administration (FDA) who ...
Quick apply
Washington, DC ยท Remote
Currently 100% remote. Please be aware that the workplace type allowed is approved by the client ... The Medical Editor will support scientists at the US Food and Drug Administration (FDA) who ...
College Park, MD ยท 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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College Park, MD ยท 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.
Remote (USA or India) Engagement: Contract (Part-Time) About the Role We are seeking an experienced ... Demonstrated capability to work with engineering, data science, and clinical teams * Excellent ...
Remote (USA or India) Engagement: Contract (Part-Time) About the Role We are seeking an experienced ... Demonstrated capability to work with engineering, data science, and clinical teams * Excellent ...
FL ยท 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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FL ยท 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 ...
Petersburg, VA ยท On-site +1
$89K - $122K/yr
... FDA meetings and inspections; defend bioassay and biological methods, based on Protein Chemistry ... remote work style with travel to Civica's Petersburg, Virginia manufacturing facility and Lehi ...
Petersburg, VA ยท On-site +1
$89K - $122K/yr
... FDA meetings and inspections; defend bioassay and biological methods, based on Protein Chemistry ... remote work style with travel to Civica's Petersburg, Virginia manufacturing facility and Lehi ...
This is a remote position. Now that you know what we're looking for in talent, let us tell you why ... Demonstrated leadership in analytical validation and regulatory submissions (CLIA, CAP, FDA, NYDoH ...
This is a remote position. Now that you know what we're looking for in talent, let us tell you why ... Demonstrated leadership in analytical validation and regulatory submissions (CLIA, CAP, FDA, NYDoH ...
Birmingham, AL ยท Remote
$50 - $60/hr
Prepare safety narratives and case documentation in accordance with FDA and global guidelines ... About Us We are a confidential global life sciences partner supporting pharmaceutical companies ...
Birmingham, AL ยท Remote
$50 - $60/hr
Prepare safety narratives and case documentation in accordance with FDA and global guidelines ... About Us We are a confidential global life sciences partner supporting pharmaceutical companies ...
Washington, DC ยท Remote
Food and Drug Administration (FDA). This position will contribute to the design, implementation ... Location Fully Remote; the selected candidate will work during DCG's core Eastern Standard Time ...
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Washington, DC ยท Remote
Food and Drug Administration (FDA). This position will contribute to the design, implementation ... Location Fully Remote; the selected candidate will work during DCG's core Eastern Standard Time ...
Baltimore, MD ยท Remote
Food and Drug Administration (FDA). This position will contribute to the design, implementation ... Location Fully Remote; the selected candidate will work during DCG's core Eastern Standard Time ...
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Baltimore, MD ยท Remote
Food and Drug Administration (FDA). This position will contribute to the design, implementation ... Location Fully Remote; the selected candidate will work during DCG's core Eastern Standard Time ...
New Haven, CT ยท On-site +1
Food and Drug Administration (FDA) accepted the New Drug Application (NDA) for vepdegestrant- an ... New Haven, CT or a remote role based within the U.S. Principal Responsibilities Key ...
New Haven, CT ยท On-site +1
Food and Drug Administration (FDA) accepted the New Drug Application (NDA) for vepdegestrant- an ... New Haven, CT or a remote role based within the U.S. Principal Responsibilities Key ...
Food and Drug Administration (FDA) accepted the New Drug Application (NDA) for vepdegestrant- an ... in New Haven, CT or a remote role based within the U.S.Principal ResponsibilitiesKey ...
Food and Drug Administration (FDA) accepted the New Drug Application (NDA) for vepdegestrant- an ... in New Haven, CT or a remote role based within the U.S.Principal ResponsibilitiesKey ...
This is a remote customer facing position covering a Massachusetts territory. Residency in either ... Deep understanding of bioprocessing workflows, cGMP principles, and regulatory expectations (FDA ...
This is a remote customer facing position covering a Massachusetts territory. Residency in either ... Deep understanding of bioprocessing workflows, cGMP principles, and regulatory expectations (FDA ...
This is a remote customer facing position covering a Massachusetts territory. Residency in either ... Deep understanding of bioprocessing workflows, cGMP principles, and regulatory expectations (FDA ...
This is a remote customer facing position covering a Massachusetts territory. Residency in either ... Deep understanding of bioprocessing workflows, cGMP principles, and regulatory expectations (FDA ...
This is a remote customer facing position covering a Massachusetts territory. Residency in either ... Deep understanding of bioprocessing workflows, cGMP principles, and regulatory expectations (FDA ...
This is a remote customer facing position covering a Massachusetts territory. Residency in either ... Deep understanding of bioprocessing workflows, cGMP principles, and regulatory expectations (FDA ...
This is a remote customer facing position covering a Massachusetts territory. Residency in either ... Deep understanding of bioprocessing workflows, cGMP principles, and regulatory expectations (FDA ...
This is a remote customer facing position covering a Massachusetts territory. Residency in either ... Deep understanding of bioprocessing workflows, cGMP principles, and regulatory expectations (FDA ...
Familiarity with regulatory expectations (FDA/ICH) for nonclinical development. Preferred ... We are a remote-first company, with occasional travel for in-person team meetings or scientific ...
Familiarity with regulatory expectations (FDA/ICH) for nonclinical development. Preferred ... We are a remote-first company, with occasional travel for in-person team meetings or scientific ...
This is a remote position within the US. Job Duties/Responsibilities * Define technical strategy ... CMS, FDA, HIPAA, or AI governance * Prior experience at leading AI-native companies or research ...
This is a remote position within the US. Job Duties/Responsibilities * Define technical strategy ... CMS, FDA, HIPAA, or AI governance * Prior experience at leading AI-native companies or research ...
Preparing international regulatory submissions and FDA submissions which may include device 510(k ... Scientific or engineering field preferred. 5+ years of medical device regulatory affairs experience.
Preparing international regulatory submissions and FDA submissions which may include device 510(k ... Scientific or engineering field preferred. 5+ years of medical device regulatory affairs experience.
$150K - $170K/yr
Remote Essential Functions * Provide scientific leadership for the planning, design, and ... Strong knowledge of ICH-GCP guidelines, FDA/EMA regulations, and clinical trial methodology.
$150K - $170K/yr
Remote Essential Functions * Provide scientific leadership for the planning, design, and ... Strong knowledge of ICH-GCP guidelines, FDA/EMA regulations, and clinical trial methodology.
Sr. Clinical Scientist CAMB000137 12 months contract Cambridge, MA/Remote (EST) *Please note ... with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety
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Sr. Clinical Scientist CAMB000137 12 months contract Cambridge, MA/Remote (EST) *Please note ... with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety
$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
| 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.
Full-time
Posted 5 days ago
Kaiva Tech, LLC is seeking a Medical Editor 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 Medical Editor will support scientists at the US Food and Drug Administration (FDA) who regulate gene therapy, cell therapy, tissue transplantation and other biological treatments for human diseases. The Medical Editor will format and proofread documents written by FDA scientists, format data tables, and create new data tables using data derived from regulatory submissions to the FDA. The position requires the ability to use a style guide to apply language and formatting standards, and a willingness to learn advanced features of Microsoft Word. Preferred candidates will have education or experience in a scientific or healthcare field.
Supervisory Responsibilities:
Essential Duties and Responsibilities:
As a Medical Editor your responsibilities will include, but are not limited to the following:
Required Experience and Skills:
Desired Experience and Skills:
Education:
Certificates, Licenses and Registrations:
Physical Requirements: