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Fda Researcher Jobs in Missouri (NOW HIRING)

Washington University of St. Louis

$75K - $128K/yr

Academic Programs, Accounting, Business Administration, Clinical Research Coordination, Clinical Research Methods, Compliance Requirements, Employee Management, FDA Compliance, FDA Regulations ...

Jobtailor

Regulatory Compliance Lead

California, MO · On-site

$150 - $190/hr

* Develops and maintains fit-for-purpose regulatory compliance frameworks for consumer, research, and ... Working knowledge of applicable FDA guidance including FDA QMSR * Familiarity with ISO 13485:2016 ...

Washington University of St. Louis

Knowledge of grant compliance and FDA regulations. * Familiarity with University systems ... Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals ...

QPS, LLC

Clinical Pharmacist

Springfield, MO · On-site

$111K - $133K/yr

Experience in a hospital, clinical, or research pharmacy environment preferred. * Knowledge of FDA, ICH, GCP, and applicable pharmacy regulations. * Strong attention to detail and documentation ...

QPS

Clinical Pharmacist

Springfield, MO · On-site

$107K - $128K/yr

Experience in a hospital, clinical, or research pharmacy environment preferred. * Knowledge of FDA, ICH, GCP, and applicable pharmacy regulations. * Strong attention to detail and documentation ...

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All JobsFda Researcher JobsFda Researcher Jobs in Missouri

Fda Researcher information

See Missouri salary details

$28.1K

$106.1K

$154.3K

How much do fda researcher jobs pay per year?

As of Aug 29, 2026, the average yearly pay for fda researcher in Missouri is $106,090.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,800.00 and $144,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an FDA researcher?

To thrive as an FDA Researcher, you need a strong background in biological sciences, chemistry, or a related field, often supported by an advanced degree (MS or PhD). Familiarity with laboratory information management systems (LIMS), regulatory databases, and compliance certifications such as Good Laboratory Practice (GLP) is typically required. Critical thinking, attention to detail, and clear scientific communication are vital soft skills in this role. These competencies are essential for ensuring research integrity, regulatory compliance, and the advancement of public health.

What are some common challenges FDA researchers face when conducting regulatory studies?

FDA researchers often encounter challenges related to balancing scientific rigor with regulatory timelines. Strict protocols and documentation requirements can make study design and execution more complex, especially when coordinating with multiple stakeholders such as review teams and external partners. Additionally, researchers must stay updated on evolving regulatory guidelines and policies, which requires ongoing professional development. Effective communication and adaptability are key to overcoming these obstacles while ensuring that research supports public health objectives.

How much do FDA researchers make?

FDA researchers typically earn a median annual salary of around $70,000 to $120,000, depending on experience, education, and specific role. Entry-level positions may start lower, while senior or specialized roles can exceed this range, often requiring relevant scientific or regulatory expertise.

What does a FDA researcher do?

An FDA researcher conducts scientific studies and analyzes data related to food, drugs, medical devices, or cosmetics to ensure safety and efficacy. They often work in laboratories, review research protocols, and collaborate with regulatory teams to support approval processes and policy development.

What cities in Missouri are hiring for Fda Researcher jobs?

Cities in Missouri with the most Fda Researcher job openings:

Fda Researcher jobs near you

Director, Physician Researcher - Evidence Generation & Registries

Jobtailor

California, MO • On-site

$180 - $300/hr

Other

Posted 13 days ago

Job description

  • Lead the design of registries, observational studies, and pragmatic real-world evidence studies, including protocol development, endpoint selection, statistical analysis planning, and data collection instruments.
  • Shape Verily's evidence generation strategy and standards across clinical programs, digital health products, and care delivery models.
  • Serve as the primary clinical point of contact for external customers, investigators, and partners.
  • Present study design rationale and represent Verily at conferences and advisory boards.
  • Oversee the responsible use of AI-enabled research tools, evaluating outputs for accuracy, bias, and clinical validity.
  • Partner with biostatistics, epidemiology, data science, product, regulatory, and commercial teams.
  • Mentor junior clinical and research staff.
Requirements
  • MD, DO, or equivalent doctoral-level degree with active or eligible medical licensure.
  • 10+ years of experience in evidence generation, real-world evidence, clinical outcomes research, clinical development, or medical affairs in a pharmaceutical, biotech, healthcare technology, or CRO environment.
  • Experience designing and leading observational studies, registries, or pragmatic clinical trials using real-world data sources, including claims, EHR, and patient-reported outcomes.
  • Experience in a customer- or partner-facing role leading scientific discussions with external investigators, KOLs, and institutional stakeholders.
  • Experience evaluating AI-enabled tools in a clinical research, registry, or real-world data context.
  • Advanced degree such as MPH, MSCE, or similar in epidemiology, clinical research, or public health preferred.
  • Authorship of peer-reviewed publications involving observational or registry data and experience presenting at national conferences preferred.
  • Working knowledge of GCP, FDA real-world evidence guidance, ISPOR/ISPE good practice standards, IRB protocol development, and data privacy requirements including HIPAA and GDPR preferred.
  • Experience mentoring or managing clinical, scientific, research, or analytics talent preferred.
  • Must not require employer-sponsored work authorization now or in the future for employment in the United States.
Core Competencies

Demonstrates expertise in designing and leading registries and observational studies, with a strong focus on real-world evidence generation and clinical outcomes research. Possesses advanced knowledge of regulatory standards and the responsible use of AI-enabled research tools in clinical settings.

Highest-signal resume keywords
  • MD, DO, Or Equivalent Doctoral-Level Degree
  • 10+ Years Of Experience In Evidence Generation
  • Experience Designing Observational Studies
  • Working Knowledge Of GCP And FDA Real-World Evidence Guidance
  • Experience Mentoring Clinical Or Research Staff
ATS Optimization KeywordsHard Skills
  • Protocol Development
  • Statistical Analysis Planning
  • Data Collection Instruments
  • Clinical Outcomes Research
  • Real-World Data Analysis
  • AI-Enabled Tool Evaluation
  • EHR Data Utilization
  • Claims Data Analysis
  • Patient-Reported Outcomes
  • Registry Design
Soft Skills
  • Leadership
  • Mentoring
  • Communication
  • Collaboration
  • Customer Engagement
Certifications & Qualifications
  • Active Or Eligible Medical Licensure
  • Advanced Degree In Epidemiology Or Public Health
Industry Keywords
  • Clinical Development
  • Pharmaceutical
  • Biotech
  • Healthcare Technology
  • CRO Environment
  • GCP
  • HIPAA
  • GDPR
  • ISPOR/ISPE Standards
  • IRB Protocol Development
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