ZipRecruiter

Log In

1

Fda Investigator Jobs in Virginia (NOW HIRING)

Tekton Research Inc

Site Manager

Richmond, VA · On-site

Ensure site staff and investigators are apprised of awarded studies * Monitor staff performance, holding staff accountable to expectations of role * Ensures staff complies with study protocols, FDA ...

Tekton Research Inc

Site Manager

Midlothian, VA · On-site

Ensure site staff and investigators are apprised of awarded studies * Monitor staff performance, holding staff accountable to expectations of role * Ensures staff complies with study protocols, FDA ...

Alcanza Clinical Research

$23.50 - $31.25/hr

Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA ...

next page

Showing results 1-20

All JobsFda Investigator JobsFda Investigator Jobs in Virginia

Fda Investigator information

See Virginia salary details

$31.7K

$74.7K

$129.9K

How much do fda investigator jobs pay per year?

As of Sep 8, 2026, the average yearly pay for fda investigator in Virginia is $74,678.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,000.00 and $97,700.00 per year, depending on experience, location, and employer.

What does an FDA Investigator do?

An FDA Investigator is responsible for inspecting facilities that manufacture, process, or distribute regulated products, including food, drugs, medical devices, and cosmetics. They ensure compliance with federal regulations, identify violations, and document findings through reports. Investigators may also collect samples, review records, and participate in enforcement actions when necessary. Their work helps protect public health by ensuring the safety, efficacy, and quality of products entering the market.

What does a typical day look like for an FDA Investigator?

A typical day for an FDA Investigator involves conducting on-site inspections of food, drug, medical device, or cosmetic manufacturers to ensure compliance with federal regulations. Investigators review production processes, collect samples, examine records, and interview facility staff to assess safety and quality standards. The role often includes significant report writing and follow-up activities to document findings and recommend corrective actions. While much of the work is independent, FDA Investigators also collaborate closely with colleagues, regulatory officials, and industry representatives to resolve issues and maintain public health standards.

What are the key skills and qualifications needed to thrive in the FDA Investigator position, and why are they important?

To thrive as an FDA Investigator, you need a background in science or public health, strong analytical skills, and often a bachelor's degree in a related field. Familiarity with regulatory databases, laboratory sampling equipment, and federal inspection protocols is typically required. Effective communication, meticulous attention to detail, and strong organizational skills help investigators excel in documenting findings and interacting with diverse stakeholders. These attributes are crucial for ensuring compliance with federal regulations and protecting public health.

How much money do FDA investigators make?

FDA investigators typically earn a median annual salary of around $70,000 to $90,000, depending on experience, location, and level of education. Entry-level investigators may start at lower salaries, while those with advanced certifications or extensive experience can earn higher wages, often with benefits such as health insurance and retirement plans.

How to become an FDA investigator?

To become an FDA investigator, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or pharmacy, along with experience in regulatory or scientific work. They must also pass the FDA's specialized training program and meet background check requirements. Strong analytical skills, attention to detail, and knowledge of regulatory guidelines are essential for this role.

What are popular job titles related to Fda Investigator jobs in Virginia?

For Fda Investigator jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Fda Investigator jobs in Virginia look for?

The top searched job categories for Fda Investigator jobs in Virginia are:

What cities in Virginia are hiring for Fda Investigator jobs?

Cities in Virginia with the most Fda Investigator job openings:

Fda Investigator jobs near you
Infographic showing various Fda Investigator job openings in Virginia as of September 2026, with employment types broken down into 1% As Needed, 77% Full Time, 18% Part Time, 3% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $74,678 per year, or $35.9 per hour.

FDA Program Administrator/Clinical Research Monitor

Vcu Rrtc

Richmond, VA • On-site

$60 - $80/hr

Other

Medical, Retirement

Posted 6 days ago

Key responsibilities

  • Develop monitoring plans for new sponsor-investigator clinical trials and studies approved through the radioactive drug research committee (RDRC).

  • Perform risk-based monitoring, author monitoring confirmation letters, follow-up reports, and assist study teams in authoring CAPAs as needed.

  • Draft and submit FDA submissions such as IND/IDE exemption, initial submissions, amendments, annual reports, safety events, closures, and emergency use requests, and assist in responding to FDA requests for information.

Job description

Advertising Summary:

Department Summary: At the VCU Office of the Vice President for Research and Innovation, our mission is to foster transformative research, discovery, and innovation at Virginia Commonwealth University through excellence in service.

We partner with faculty in all schools and departments as they seek funding, plan studies, establish collaborations, calculate budgets, submit grant applications, negotiate industry contracts, and secure patents and licensing agreements.

Our commitment to supporting and elevating the research community at VCU has resulted in record levels of sponsored research and has placed VCU among the nation’s premier public research universities.

Through our passion for discovery and willingness to take on challenges, we continue to advance the work that matters most and position the university as a national leader in research, innovation, creativity, and scholarship.

Duties & Responsibilities:

FDA program Administrator/Clinical Research Monitor

Responsibilities:

  • Perform risk-based monitoring
  • Develop monitoring plans for new sponsor-investigator clinical trials and studies that get approved through the radioactive drug research committee (RDRC)
  • Author monitoring confirmation letters and follow-up reports
  • Assist study teams in authoring CAPAs as needed
  • Maintain a dashboard to provide metrics on monitoring visits and to identify areas of risk and opportunities for training
  • Serve as a back-up for the following:
    • Draft and submit the following submissions to the FDA on behalf of the sponsor-investigators: IND/IDE exemption, IND/IDE initial submission, amendments, annual reports, safety events, closures and single patient/emergency use
    • Manage high volume of submissions at any given time with multiple urgent deadlines
    • Assist sponsor-investigator in responding to FDA’s requests for information
    • Draft and submit the following submissions to the IRB: single patient/emergency use (initial submission, reportable new information, continuing reviews, closure)
    • Maintain dashboard that provides metrics on submission time, requests for submissions and on upcoming annual reports
  • Train investigators/study teams on how to use Veeva SiteVault, eTMF and EDC and serve as a resource for questions on using the system
  • Provide best practices on how to perform aspects of clinical research
  • Assist in FDA inspections as neededOther tasks as needed

Qualifications:

Minimum Qualifications:

Demonstrated ability to work in and foster an environment of respect, professionalism and civility with a population of faculty, staff, and students from all backgrounds and experiences, or a commitment to do so as a staff member at VCU.

Only applicants who do not require current or future sponsorship for employment will be considered

  • 1-2 years of relevant work experience involving clinical research, monitoring and the FDA
  • Bachelor’s degree
  • Familiarity with the various types of FDA submissions including IND, IDEs and expanded access
  • Ability to handle high volume of studies with increasing complex study designs
  • Ability to handle high volume of FDA submissions with consistently changing deadlines
  • Experience working as a clinical research coordinator or in a role involved in clinical research
  • Ability to communicate clearly and effectively both verbally and in writing
  • Knowledge of FDA and ICH-GCP regulations
  • Ability to maintain integrity, objectivity, independence and confidentialityAbility to manage workload to work efficiently and meet deadlines as needed
  • Ability to interact with individuals of various positions and with an array of personalities
  • Experience utilizing electronic systems that are utilized in clinical research such as a CTMS, electronic investigator site file and EMR
  • Experience working with different indications
  • Have monitored clinical trials

Preferred Qualifications:

  • 3+ years of relevant work experience involving clinical research, monitoring and the FDA
  • Have monitored clinical trials
  • Experience with radiation oncology or radiopharmaceutical studies
  • Experience submitting various types of FDA submissions to the FDA for research including initial submissions, annual reports and safety reports of IND, IDEs and expanded access applications
  • Experience utilizing electronic systems that are utilized in clinical research such as a CTMS, electronic investigator site file and EMR
  • Experience working with different indications including addiction, oncology and non-oncology
  • Relevant professional certification(s) in aspects of clinical research

Salary Range:70,000 - 80,000

Benefits: All full-time university staff are eligible for VCU’s robust benefits package that includes comprehensive health benefits, paid annual and holiday leave, generous tuition benefits, retirement planning and savings options, tax-deferred annuity and cash match programs, employee discounts, well-being resources, abundant opportunities for career development and advancement, and more.

Unit: Office of the Vice President for Research & Innovation

Department: Strategy and Regulatory Affairs

FLSA Exemption Status: Exempt

Hours per Week: 40

Restricted Position: Yes

ORP Eligible: No

Flexible Work Arrangement: Hybrid

University Job Title: 25234N - Sr Specialist LG 1 - Open

#J-18808-Ljbffr

Apply