1

Fda Investigator Jobs (NOW HIRING)

Principal Investigator Salary Range: $200 - $285k (DOE) Location: Baltimore, MD (On-site) About ... Ensure studies are conducted in compliance with ICH-GCP, FDA regulations, and applicable guidelines

Principal Investigator

Baltimore, MD · On-site

$200K - $285K/yr

Principal Investigator Salary Range: $200 - $285k (DOE) Location: Baltimore, MD (On-site) About ... Ensure studies are conducted in compliance with ICH-GCP, FDA regulations, and applicable guidelines

Becoming commissioned/credentialed with a produce category by FDA is a requirement of this job and ... Some experience with investigative procedures including developing evidence, establishing ...

Sub-Investigator

Plymouth, MA

$50K - $51K/yr

Sub-Investigator (Nurse Practitioner) The Sub-Investigator is accountable and responsible for ... Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs ...

next page

Showing results 1-20

Fda Investigator information

See salary details

$32K

$75.3K

$131K

How much do fda investigator jobs pay per year?

As of Jun 17, 2026, the average yearly pay for fda investigator in the United States is $75,325.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $98,500.00 per year, depending on experience, location, and employer.

How do you become a FDA inspector?

To become an FDA inspector, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or food science, along with experience in food safety, pharmaceuticals, or related areas. They must also pass a written exam and a background check, and may need to complete specialized training provided by the FDA. Strong analytical skills, attention to detail, and knowledge of regulatory standards are essential for the role.

How much do FDA drug investigators make?

FDA drug investigators typically earn a salary ranging from $70,000 to $120,000 annually, depending on experience, education, and location. They often hold a bachelor's degree in a relevant field and may require specialized training or certifications to perform inspections and investigations effectively.

What do FDA auditors make?

FDA investigators, also known as FDA auditors, typically earn a salary ranging from $70,000 to $120,000 annually, depending on experience, location, and level of responsibility. They often hold a background in science, healthcare, or regulatory affairs and may require certifications such as the Certified Regulatory Compliance Manager (CRCM).

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 an FDA investigator do?

An FDA investigator conducts inspections of manufacturing facilities, laboratories, and distribution sites to ensure compliance with food, drug, and medical device regulations. They review records, collect samples, and document violations to protect public health and enforce federal laws. The role often requires knowledge of regulatory standards and attention to detail.

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.

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.

More about Fda Investigator jobs
What cities are hiring for Fda Investigator jobs? Cities with the most Fda Investigator job openings:
What are the most commonly searched types of Fda Investigator jobs? The most popular types of Fda Investigator jobs are:
What states have the most Fda Investigator jobs? States with the most job openings for Fda Investigator jobs include:
Infographic showing various Fda Investigator job openings in the United States as of June 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $75,325 per year, or $36.2 per hour.
Principal Investigator

Principal Investigator

Pharmaron

Baltimore, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 19 days ago


Job description

Position: Principal Investigator

Salary Range: $200 - $285k (DOE)

Location: Baltimore, MD (On-site)

About Pharmaron

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.

We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit www.pharmaron.com.

Job Overview

Pharmaron is seeking an experienced physician to serve as a Principal Investigator within our growing Phase I Clinical Research Unit in Baltimore, Maryland.

This is a unique opportunity for a board-certified physician who is passionate about advancing medicine through clinical research while maintaining a strong focus on participant safety and quality care. Clinical research experience is welcomed but not required. Physicians with backgrounds in Internal Medicine, Family Medicine, Emergency Medicine, or related specialties are encouraged to apply.

As Principal Investigator, you will provide medical leadership for early-phase clinical studies, oversee participant safety, collaborate with sponsors and scientific teams, and help shape the future growth of our clinical research programs.

Key Responsibilities:

Clinical Leadership

  • Serve as Principal Investigator or Sub-Investigator for Phase I-III clinical studies
  • Provide medical oversight and ensure participant safety throughout study conduct
  • Review eligibility, medical histories, adverse events, and safety data
  • Conduct physical examinations and medical assessments as required

Study Execution & Scientific Collaboration

  • Partner with sponsors and internal teams on protocol review, study design, and implementation
  • Support dosing activities and ongoing medical monitoring
  • Contribute to study interpretation, reporting, and regulatory submissions
  • Provide scientific and medical consultation to project teams and clients

Regulatory & Quality Oversight

  • Ensure studies are conducted in compliance with ICH-GCP, FDA regulations, and applicable guidelines
  • Maintain protocol integrity and oversight responsibilities as listed on FDA Form 1572
  • Support inspections, audits, and regulatory interactions when required

Team Leadership

  • Mentor and guide Clinical Research Coordinators, nurses, and study staff
  • Promote a culture of participant safety, quality, and operational excellence
  • Collaborate closely with Medical, Clinical Operations, Pharmacy, Laboratory, and Business Development teams

What We're Looking For:

Required Qualifications

  • MD or DO degree from an accredited medical school
  • Board Certification in a recognized specialty
  • Active and unrestricted medical license
  • Minimum 5 years of clinical practice experience
  • Current CPR and ACLS certifications
  • Strong understanding of patient care, medical ethics, and clinical decision-making
  • Excellent communication and leadership skills

Preferred Qualifications

  • Previous clinical research experience as a Principal Investigator, Sub-Investigator, or treating physician
  • Experience supporting Phase I or early clinical development programs
  • Familiarity with ICH-GCP, FDA regulations, and clinical trial operations
  • DEA registration
  • Background in Internal Medicine, Family Medicine, or Emergency Medicine

Why Pharmaron?

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:

  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.