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Remote Fda Jobs in Kansas (NOW HIRING)

PICTOR LABS INC

$89.70K - $123.20K/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 ...

Norstella

Sales Director

Topeka, KS · Remote

Remote, United States Date Posted: Apr 23, 2026 Employment Type: Full Time Job ID: R-1754 ... the FDA, and payers. By providing critical proprietary data supporting AI-driven workflows ...

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$23K

$78.3K

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How much do remote fda jobs pay per year?

As of May 30, 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 job?

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 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 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.
More about Remote Fda jobs
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:
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What cities in Kansas are hiring for Remote Fda jobs? Cities in Kansas with the most Remote Fda job openings:
Remote Fda jobs near you
Infographic showing various Remote Fda job openings in Kansas as of May 2026, with employment types broken down into 89% Full Time, and 11% Contract. Highlights an 100% Remote job distribution, with an average salary of $78,267 per year, or $37.6 per hour.

Oncology Clinical Researcher

Alignerr

Kansas City, KS • Remote

Full-time

Posted 9 days ago

Job description

Oncology Clinical Researcher (AI Training)
About the Role
What if your deep expertise in cancer clinical trials could directly shape how AI understands and reasons about oncology - influencing research that could one day transform patient outcomes worldwide?
We're looking for experienced Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI development. You'll work with leading AI research teams to ensure that oncology trial data, insights, and outputs meet the highest scientific, regulatory, and clinical standards.
This is a fully remote, flexible contract role built for working oncology professionals and researchers who want to apply their expertise beyond the lab or clinic.
  • Organization
    : Alignerr
  • Type
    : Hourly Contract
  • Location
    : Remote
  • Commitment
    : 10-40 hours/week
    • What You'll Do
    • Design and evaluate oncology clinical trial frameworks - including study protocols, patient enrollment criteria, and regulatory compliance standards - for use in AI training workflows
    • Analyze cancer trial data across safety, efficacy, and biomarker endpoints to assess treatment performance and clinical relevance
    • Translate trial outcomes into clear regulatory and scientific narratives aligned with FDA/EMA submission standards
    • Review and evaluate AI-generated clinical insights, flagging inaccuracies and ensuring outputs reflect real-world oncology practice
    • Provide expert judgment on how well AI models interpret and reason about complex oncology data
    • Work independently and asynchronously - fully on your own schedule
    Who You Are
    • Experienced in designing and managing oncology clinical trials from protocol development through data readout
    • Strong background in analyzing oncology clinical data - endpoints, safety profiles, biomarkers, and statistical outputs
    • Familiar with regulatory submission standards for agencies such as the FDA or EMA
    • Detail-oriented, methodical, and confident in making expert clinical judgments
    • Comfortable working independently on structured, task-based assignments
    Nice to Have
    • Prior experience with data annotation, data quality evaluation, or AI model assessment workflows
    • Background in translational oncology, precision medicine, or biomarker-driven trial design
    • Experience authoring or reviewing clinical study reports, publications, or regulatory dossiers
    • Familiarity with AI tools or clinical data platforms as an end user
    Why Join Us
    • Work directly on frontier AI systems being developed alongside the world's leading research labs
    • Influence how AI models understand, interpret, and reason about real oncology data
    • Fully remote and flexible - work when and where it suits you
    • Freelance autonomy with the structure of meaningful, expert-level work
    • Contribute to AI-driven oncology research with genuine potential to impact cancer care
    • Potential for ongoing work and contract extension as new projects launch

Apply