... 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 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 ...
Lead iOS Engineer: Clinical Platform
Fort Lauderdale, FL · On-site +1
$133K/yr
Experience with healthcare, telehealth, or clinical software, particularly FDA-adjacent or EHR ... Remote
Lead iOS Engineer: Clinical Platform
Fort Lauderdale, FL · On-site +1
$133K/yr
Experience with healthcare, telehealth, or clinical software, particularly FDA-adjacent or EHR ... Remote
Field Service Engineer II - Orlando, FL
Orlando, FL · Remote
$30 - $43/hr
Document and complete service administration activities in a timely manner to follow ISO, FDA, and ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...
Field Service Engineer II - Orlando, FL
Orlando, FL · Remote
$30 - $43/hr
Document and complete service administration activities in a timely manner to follow ISO, FDA, and ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...
S. FDA for a monoclonal antibody (mAb) in its pipeline of innovative antibody candidates. In ... Remote - Orlando/Tampa FL Position Summary: At Invivyd, we're building a new category of infectious ...
S. FDA for a monoclonal antibody (mAb) in its pipeline of innovative antibody candidates. In ... Remote - Orlando/Tampa FL Position Summary: At Invivyd, we're building a new category of infectious ...
Deep understanding of the healthcare/pharmaceutical media landscape, including FDA approvals and ... Comfortable working in and contributing to a fully remote team environment. * Bachelor's degree ...
Deep understanding of the healthcare/pharmaceutical media landscape, including FDA approvals and ... Comfortable working in and contributing to a fully remote team environment. * Bachelor's degree ...
Technician Production Operations
Hialeah, FL · On-site +1
$15.50 - $19.50/hr
Experience working in a regulated environment (e.g., GMP, GLP, FDA). Beckman Coulter Diagnostics, a ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...
Technician Production Operations
Hialeah, FL · On-site +1
$15.50 - $19.50/hr
Experience working in a regulated environment (e.g., GMP, GLP, FDA). Beckman Coulter Diagnostics, a ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...
This position may be performed in a hybrid in-office/remote setting upon successful completion of ... Knowledge of HIPAA, OSHA, an FDA compliance. * Understanding of basic reproductive physiology.
Quick apply
This position may be performed in a hybrid in-office/remote setting upon successful completion of ... Knowledge of HIPAA, OSHA, an FDA compliance. * Understanding of basic reproductive physiology.
Sr. Oncore Analyst -Oncology - Remote (Full Time, Days)
Miami, FL · On-site +1
$110K - $111K/yr
Follows NCHS RI's Standard Operating Procedures, HIPAA, and FDA guidelines for clinical research, and keeps updated on those procedures and/or guidelines. * Collaborates with Research IT on research ...
Sr. Oncore Analyst -Oncology - Remote (Full Time, Days)
Miami, FL · On-site +1
$110K - $111K/yr
Follows NCHS RI's Standard Operating Procedures, HIPAA, and FDA guidelines for clinical research, and keeps updated on those procedures and/or guidelines. * Collaborates with Research IT on research ...
Associate Director/Director, CMC Analytical Development, Separation
Fort Lauderdale, FL · On-site +1
$165K - $200K/yr
Ensure adherence to GMP, ICH, and FDA guidelines for analytical activities. * Drive continuous ... Remote
Associate Director/Director, CMC Analytical Development, Separation
Fort Lauderdale, FL · On-site +1
$165K - $200K/yr
Ensure adherence to GMP, ICH, and FDA guidelines for analytical activities. * Drive continuous ... Remote
Project Manager
Tallahassee, FL · On-site +1
Location: Remote option available - open to Savannah, GA, Tampa, FL, Miami, FL, Orlando, FL ... Ensure all designs meet applicable codes, standards, and industry regulations, including GMP, FDA ...
Project Manager
Tallahassee, FL · On-site +1
Location: Remote option available - open to Savannah, GA, Tampa, FL, Miami, FL, Orlando, FL ... Ensure all designs meet applicable codes, standards, and industry regulations, including GMP, FDA ...
Project Manager - Design
Tampa, FL · On-site +1
Location: Remote option available - open to Savannah, GA, Tampa, FL, Miami, FL, Orlando, FL ... Ensure all designs meet applicable codes, standards, and industry regulations, including GMP, FDA ...
Project Manager - Design
Tampa, FL · On-site +1
Location: Remote option available - open to Savannah, GA, Tampa, FL, Miami, FL, Orlando, FL ... Ensure all designs meet applicable codes, standards, and industry regulations, including GMP, FDA ...
Project Manager
Orlando, FL · On-site +1
Location: Remote option available - open to Savannah, GA, Tampa, FL, Miami, FL, Orlando, FL ... Ensure all designs meet applicable codes, standards, and industry regulations, including GMP, FDA ...
Project Manager
Orlando, FL · On-site +1
Location: Remote option available - open to Savannah, GA, Tampa, FL, Miami, FL, Orlando, FL ... Ensure all designs meet applicable codes, standards, and industry regulations, including GMP, FDA ...
Project Manager - Design
Miami, FL · On-site +1
Location: Remote option available - open to Savannah, GA, Tampa, FL, Miami, FL, Orlando, FL ... Ensure all designs meet applicable codes, standards, and industry regulations, including GMP, FDA ...
Project Manager - Design
Miami, FL · On-site +1
Location: Remote option available - open to Savannah, GA, Tampa, FL, Miami, FL, Orlando, FL ... Ensure all designs meet applicable codes, standards, and industry regulations, including GMP, FDA ...
Director, Scientific Business Development
Miami, FL · On-site +1
Familiarity with FDA/EMA regulatory pathways for combination products * IP and deal-structuring ... Hybrid or remote; travel ~25% Compensation: Competitive with bonus and equity potential
Director, Scientific Business Development
Miami, FL · On-site +1
Familiarity with FDA/EMA regulatory pathways for combination products * IP and deal-structuring ... Hybrid or remote; travel ~25% Compensation: Competitive with bonus and equity potential
Clinical Trial Manager, Immunology
Miami Beach, FL · On-site +1
$150K - $165K/yr
Working knowledge of relevant GCPs and FDA, EMA and MHRA regulations * Demonstrated experience ... EOE/AA/Vets #LI-Remote
Clinical Trial Manager, Immunology
Miami Beach, FL · On-site +1
$150K - $165K/yr
Working knowledge of relevant GCPs and FDA, EMA and MHRA regulations * Demonstrated experience ... EOE/AA/Vets #LI-Remote
Working knowledge of FDA guidelines and global regulatory expectations and their operational impact ... This is a remote opportunity open to candidates currently residing in the United States. IQVIA is a ...
Working knowledge of FDA guidelines and global regulatory expectations and their operational impact ... This is a remote opportunity open to candidates currently residing in the United States. IQVIA is a ...
Working knowledge of FDA guidelines and global regulatory expectations and their operational impact ... This is a remote opportunity open to candidates currently residing in the United States. IQVIA is a ...
Working knowledge of FDA guidelines and global regulatory expectations and their operational impact ... This is a remote opportunity open to candidates currently residing in the United States. IQVIA is a ...
Field Clinical Representative - Panama City, FL
Panama City, FL · Remote
$100K - $130K/yr
We are revolutionizing the sleep industry with our FDA-approved medical device, designed to reduce ... Previous Operating Room (surgical) coverage with implantable devices. #LI-Remote The salary for ...
Field Clinical Representative - Panama City, FL
Panama City, FL · Remote
$100K - $130K/yr
We are revolutionizing the sleep industry with our FDA-approved medical device, designed to reduce ... Previous Operating Room (surgical) coverage with implantable devices. #LI-Remote The salary for ...
Remote Fda information
See Florida salary details
$20.7K - $31.5K
12% of jobs
$40K is the 25th percentile. Wages below this are outliers.
$31.5K - $42.2K
17% of jobs
$42.2K - $53K
14% of jobs
The median wage is $60.3K / yr.
$53K - $63.7K
12% of jobs
$63.7K - $74.5K
12% of jobs
$84.4K is the 75th percentile. Wages above this are outliers.
$74.5K - $85.2K
11% of jobs
$85.2K - $96K
7% of jobs
$96K - $106.7K
6% of jobs
$106.7K - $117.5K
4% of jobs
$117.5K - $128.3K
4% of jobs
$128.3K - $139K
2% of jobs
$20.7K
$70.6K
$139K
How much do remote fda jobs pay per year?
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?
What are the most commonly searched types of Fda jobs in Florida?
The most popular types of Fda jobs in Florida are:
What are popular job titles related to Remote Fda jobs in Florida?
For Remote Fda jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Remote Fda jobs in Florida look for?
The top searched job categories for Remote Fda jobs in Florida are:
What cities in Florida are hiring for Remote Fda jobs?
Cities in Florida with the most Remote Fda job openings:

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 6 days ago
Danaher rating
7.7
Based on 31 frontline employees who took The Breakroom Quiz
194th of 545 rated manufacturers
Job description
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
Within Danaher the work our diagnostic businesses do saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
We're accelerating the development of cutting-edge diagnostics to solve some of the world's most pressing health challenges. Across our diagnostics operating companieswe are drivinginnovationthroughpartnerships with top academic institutions and leading players in biopharma and translational research.We're bringing the best minds together toaccelerateinnovation and unlock the full potential of the latest scientific advances. Together, we're expanding access to precision diagnostics for millions of people worldwide - and we're using our unmatched global scale and proven playbook to make it happen, from hospital labs to mobile clinics. By helping providers, patients, and families get faster, more precise diagnostic results, we're improving treatment options and saving lives.
Learn about theDanaher Business Systemwhich makes everything possible.
Principal Clinical Scientist. This role is responsible for clinical trial strategies within the US and EU regions for Danaher Diagnostics Neurodegenerative program. This role will specifically support Beckman Coulter Diagnostics and Life Sciences, operating companies of Danaher Diagnostics. You will drive strategic study designs, ensuring regulatory compliance, and achieving key milestones for critical clinical studies in these vital markets.
This position is part of the Danaher Diagnostics, Beckman Coulter Inc. organization and will be remote based (can also be onsite in Chaska MN). At Danaher Diagnostics, our vision is to be the leading provider of seamlessly connected diagnostic solutions.
In this role, you will have the opportunity to:
- Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA 510(k)/PMA, CEIVDR) across multiple diagnostic modalities.
- Act as a scientific and clinical liaison with regulatory bodies, key opinion leaders, and external sites to develop protocols, claims, and evidence plans.
- Partner crossfunctionally with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams to align clinical programs with product development and market access needs.
- Author and review clinical and regulatory documentation-including study reports, technical files, and publications-to support product clearance and commercialization.
- Build strong internal and external collaborations, mentor junior scientists, and maintain expertise in evolving regulatory standards, clinical guidelines, and diagnostic technologies
The essential requirements of the job include:
- Bachelor's degree in Life Sciences, Healthcare, or a related field with 9+ years of experience in clinical research, specifically with significant experience in US and/or EU trials, or a Master's degree with 12+ years of experience or Doctoral degree with 4+ years of same experience.
- In-depth understanding of clinical study design and methodology in the diagnostics, medical device, or pharmaceutical industry with products intended for the US and EU markets.
- Demonstrated ability to identify and solve complex issues in clinical trial conduct and scientific interpretation.
- Ability to critically review and interpret scientific and clinical trial data, and oversee the scientific aspects of study protocols and reports.
- Excellent communication (written and verbal) and interpersonal skills for collaborating with cross-functional stakeholders.
It would be a plus if you also possess previous experience in:
- Experience in study designs for diagnostic technologies (IVD) is highly preferred, specifically for Neurodegenerative Biomarkers.
- Advanced degree in Science, Healthcare, or Regulatory/Clinical Affairs.
- Professional certification in Clinical Research (e.g., SoCRA, ACRP).
Danaher Diagnostics, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at danaherbenefitsinfo.com.
This job is also eligible for bonus/incentive pay.
At Beckman Coulter Diagnostics we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide.
The annual salary range for this role is$120K-$130K.This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
The U.S. EEO posters are available here.
For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here.
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.
About Danaher
Sourced by ZipRecruiter
We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.
Industry
Medical equipment and supplies manufacturing
Company size
10,000+ Employees
Headquarters location
Washington, DC, US
Year founded
1984