$128K - $169K/yr
Interaction with clients and FDA, lead interactions with Health Authorities * Internal BD ... Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ...
$128K - $169K/yr
Interaction with clients and FDA, lead interactions with Health Authorities * Internal BD ... Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ...
$89K - $123K/yr
... meets FDA and SOC2 compliance requirements. This role offers the opportunity to work at the ... Remote US Company: Pictor Labs Employment Type: Full-time Responsibilities * Design, development ...
$89K - $123K/yr
... meets FDA and SOC2 compliance requirements. This role offers the opportunity to work at the ... Remote US Company: Pictor Labs Employment Type: Full-time Responsibilities * Design, development ...
Compliance Officers
Topeka, KS · 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 ...
Compliance Officers
Topeka, KS · 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 ...
Director of Biostatistics
Wichita, KS · 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 ...
Director of Biostatistics
Wichita, KS · 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 ...
Director of Biostatistics
Kansas City, KS · 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 ...
Director of Biostatistics
Kansas City, KS · 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 ...
Director of Biostatistics
Overland Park, KS · 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 ...
Director of Biostatistics
Overland Park, KS · 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 ...
Director of Biostatistics
Topeka, KS · 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 ...
Director of Biostatistics
Topeka, KS · 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 ...
Regulatory Affairs Specialist
Olathe, KS · 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 ...
Regulatory Affairs Specialist
Olathe, KS · 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 ...
Compliance Officers
Olathe, KS · 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 ...
Compliance Officers
Olathe, KS · 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 ...
Biostatistician
Topeka, KS · 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 ...
Biostatistician
Topeka, KS · 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 ...
Regulatory Affairs Specialist
Wichita, KS · 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 ...
Regulatory Affairs Specialist
Wichita, KS · 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 ...
Biostatistician
Olathe, KS · 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 ...
Biostatistician
Olathe, KS · 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 ...
Compliance Officers
Overland Park, KS · 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 ...
Compliance Officers
Overland Park, KS · 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 ...
Compliance Officers
Wichita, KS · 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 ...
Compliance Officers
Wichita, KS · 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 ...
Biostatistician
Wichita, KS · 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 ...
Biostatistician
Wichita, KS · 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 ...
Biostatistician
Kansas City, KS · 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 ...
Biostatistician
Kansas City, KS · 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 ...
Regulatory Affairs Specialist
Overland Park, KS · 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 ...
Regulatory Affairs Specialist
Overland Park, KS · 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 ...
Regulatory Affairs Specialist
Kansas City, KS · 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 ...
Regulatory Affairs Specialist
Kansas City, KS · 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 ...
Regulatory Affairs Specialist
Topeka, KS · 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 ...
Regulatory Affairs Specialist
Topeka, KS · 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 ...
Biostatistician
Overland Park, KS · 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 ...
Biostatistician
Overland Park, KS · 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 ...
Remote Fda information
See Kansas salary details
$23K - $34.9K
12% of jobs
$44.4K is the 25th percentile. Wages below this are outliers.
$34.9K - $46.8K
17% of jobs
$46.8K - $58.7K
14% of jobs
The median wage is $66.8K / yr.
$58.7K - $70.6K
12% of jobs
$70.6K - $82.6K
12% of jobs
$93.6K is the 75th percentile. Wages above this are outliers.
$82.6K - $94.5K
11% of jobs
$94.5K - $106.4K
7% of jobs
$106.4K - $118.3K
6% of jobs
$118.3K - $130.2K
4% of jobs
$130.2K - $142.2K
4% of jobs
$142.2K - $154.1K
2% of jobs
$23K
$78.3K
$154.1K
How much do remote fda jobs pay per year?
As of Sep 5, 2026, the average yearly pay for remote fda in Kansas is $78,267.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,472.00 and $101,539.00 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 popular job titles related to Remote Fda jobs in Kansas?
For Remote Fda jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Remote Fda jobs in Kansas look for?
The top searched job categories for Remote Fda jobs in Kansas are:
What cities in Kansas are hiring for Remote Fda jobs?
Cities in Kansas with the most Remote Fda job openings:
$128K - $169K/yr
Full-time
Medical, Retirement
Posted 8 days ago
Job description
Job Description:
Director, Regulatory Affairs
Director Regulatory Affairs, responsible for strategic and operational regulatory consulting for client companies. The Director RA will be client facing and will be responsible amongst others for:
- Strategic Advice to clients, with focus on early development through to NDA/ BLA
- Independent preparation of regulatory documentation such as US IND, NDA/BLA modules, ODD, Fast track / other designations, FDA advice requests.
- Scientific Interaction with internal cross functional teams
- Client facing & Agency point of contact: Interaction with clients and FDA, lead interactions with Health Authorities
- Internal BD & marketing facing role
Make an Impact at Veristat!
Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.
- 105+ approved therapies for marketing applications prepared by Veristat
- 480+ oncology projects in the past 5 years
- 350+ rare disease projects delivered in the past 5 years
- Flexible, inclusive culture - 70% remote workforce, 66% women-led teams
Learn more about our core valueshere!
What we offer
- The estimated hiring range for this role is $195K-223K plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.
- Benefits vary by location and may include:
- Remote working
- Flexible time off
- Paid holidays
- Medical insurance
- Tuition reimbursement
- Retirement plans
What we look for
- Bachelor's degree in science, toxicology, pharmacology, engineering or related field; Advanced Scientific degree such as Master's degree, Ph.D. or Pharm.D. preferred, with applied training relevant to clinical trials.
- 10 years of relevant experience working directly for a CRO/ Pharmaceutical Company, with a minimum 5 years of experience leading regulatory development projects.
- Thorough knowledge of International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical research.
- Excellent written and oral communication skills including grammatical and technical writing skills, and familiarity with moderately complex study designs and regulatory requirements that apply to Phase I-IV clinical trials are required.
- In-depth knowledge of the relationship and regulatory obligation of the contract research organization (CRO) industry with pharmaceutical / biotech companies.
- Demonstrated ability to lead by example with demonstrated skill for technical and supervisory leadership of staff.
- Skilled in use of computer software, including Microsoft Word and Microsoft Excel, and ability to learn new applications.
- Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a team environment.
Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
About Veristat
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
501 - 1,000 Employees
Headquarters location
Southborough, MA, US
Year founded
1994