Principal Investigator
Baltimore, MD · On-site
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
Baltimore, MD · On-site
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
Baltimore, MD · On-site
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
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
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
Brea, CA · On-site
$80K - $90K/yr
... an FDA investigator with confidence, this role was built for you. What You'll Do As the Calibration and Maintenance Supervisor, you will own two mission-critical programs and lead the team that ...
Brea, CA · On-site
$80K - $90K/yr
... an FDA investigator with confidence, this role was built for you. What You'll Do As the Calibration and Maintenance Supervisor, you will own two mission-critical programs and lead the team that ...
Boise, ID · On-site
$23.91/hr
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 ...
Boise, ID · On-site
$23.91/hr
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 ...
... an FDA investigator with confidence, this role was built for you. What You'll Do As the Calibration and Maintenance Supervisor, you will own two mission-critical programs and lead the team that ...
... an FDA investigator with confidence, this role was built for you. What You'll Do As the Calibration and Maintenance Supervisor, you will own two mission-critical programs and lead the team that ...
Washington, DC · On-site
$225K/yr
Provide legal guidance during FDA inspections, investigations, and enforcement actions * Conduct legal research and analysis on FDA laws, regulations, and enforcement trends * Collaborate with ...
Washington, DC · On-site
$225K/yr
Provide legal guidance during FDA inspections, investigations, and enforcement actions * Conduct legal research and analysis on FDA laws, regulations, and enforcement trends * Collaborate with ...
$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 ...
$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 ...
$40K - $40K/yr
Position Summary The Principal Investigator (PI) is responsible for the overall design, conduct ... FDA regulations, ICH-GCP guidelines, sponsor requirements, and institutional policies. The PI ...
$40K - $40K/yr
Position Summary The Principal Investigator (PI) is responsible for the overall design, conduct ... FDA regulations, ICH-GCP guidelines, sponsor requirements, and institutional policies. The PI ...
... Investigator (PI) is responsible for the overall conduct, oversight, and integrity of clinical ... FDA regulations (21 CFR Parts 50, 54, 56, 312/812 as applicable) * IRB/IBC requirements * Ensure ...
... Investigator (PI) is responsible for the overall conduct, oversight, and integrity of clinical ... FDA regulations (21 CFR Parts 50, 54, 56, 312/812 as applicable) * IRB/IBC requirements * Ensure ...
Investigators FLSA Status: Exempt Come join our team and make a difference as we blaze the way into ... Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times.
Investigators FLSA Status: Exempt Come join our team and make a difference as we blaze the way into ... Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times.
A Manufacturing Process Investigator is a professional who conducts thorough investigations into ... FDA, GMP) and industry best practices. Collaborate with key stakeholders to ensure procedural ...
A Manufacturing Process Investigator is a professional who conducts thorough investigations into ... FDA, GMP) and industry best practices. Collaborate with key stakeholders to ensure procedural ...
Provide legal guidance during FDA inspections, investigations, and enforcement actions * Conduct legal research and analysis on FDA laws, regulations, and enforcement trends * Collaborate with ...
Provide legal guidance during FDA inspections, investigations, and enforcement actions * Conduct legal research and analysis on FDA laws, regulations, and enforcement trends * Collaborate with ...
Austin, TX · On-site
Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times ... Oversee Sub-Investigators and recruitment team. Education/Experience: * One to two years of ...
New
Quick apply
Austin, TX · On-site
Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times ... Oversee Sub-Investigators and recruitment team. Education/Experience: * One to two years of ...
New
Georgetown, TX · On-site
Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times ... Oversee Sub-Investigators and recruitment team. Education/Experience: * One to two years of ...
New
Quick apply
Georgetown, TX · On-site
Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times ... Oversee Sub-Investigators and recruitment team. Education/Experience: * One to two years of ...
New
Austin, TX · On-site
Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times ... Oversee Sub-Investigators and recruitment team. Education/Experience: * One to two years of ...
New
Quick apply
Austin, TX · On-site
Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times ... Oversee Sub-Investigators and recruitment team. Education/Experience: * One to two years of ...
New
Georgetown, TX · On-site
Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times ... Oversee Sub-Investigators and recruitment team. Education/Experience: * One to two years of ...
New
Quick apply
Georgetown, TX · On-site
Adhere to study protocols, FDA regulations, and Good Clinical Practice (GCP) at all times ... Oversee Sub-Investigators and recruitment team. Education/Experience: * One to two years of ...
New
Lutherville Timonium, MD · On-site
$55 - $65/hr
Ensure all study activities comply with GCP, FDA, and IRB requirements. * Review source documents ... Work closely with the Principal Investigator, Research Coordinator, and study staff. * Provide ...
Quick apply
Lutherville Timonium, MD · On-site
$55 - $65/hr
Ensure all study activities comply with GCP, FDA, and IRB requirements. * Review source documents ... Work closely with the Principal Investigator, Research Coordinator, and study staff. * Provide ...
Execution of Form FDA 1572 for each study, and compliance with Form FDA 1572 requirements for ... Assuring that a qualified physician (PI or sub-investigator) is responsible for all trial-related ...
Execution of Form FDA 1572 for each study, and compliance with Form FDA 1572 requirements for ... Assuring that a qualified physician (PI or sub-investigator) is responsible for all trial-related ...
Lutherville Timonium, MD · On-site
$55 - $65/hr
Ensure all study activities comply with GCP, FDA, and IRB requirements. * Review source documents ... Work closely with the Principal Investigator, Research Coordinator, and study staff. * Provide ...
Quick apply
Lutherville Timonium, MD · On-site
$55 - $65/hr
Ensure all study activities comply with GCP, FDA, and IRB requirements. * Review source documents ... Work closely with the Principal Investigator, Research Coordinator, and study staff. * Provide ...
... g., FDA, GMP) and industry best practices. Ø Collaborate with key stakeholders to ensure ... and investigations. Ø Strong analytical and problem-solving abilities. Ø Proficiency in root ...
... g., FDA, GMP) and industry best practices. Ø Collaborate with key stakeholders to ensure ... and investigations. Ø Strong analytical and problem-solving abilities. Ø Proficiency in root ...
$32K - $41K
7% of jobs
$41K - $50K
14% of jobs
$51.5K is the 25th percentile. Wages below this are outliers.
$50K - $59K
24% of jobs
The median wage is $63.5K / yr.
$59K - $68K
9% of jobs
$68K - $77K
5% of jobs
$77K - $86K
15% of jobs
$86.8K is the 75th percentile. Wages above this are outliers.
$86K - $95K
3% of jobs
$95K - $104K
6% of jobs
$104K - $113K
4% of jobs
$113K - $122K
12% of jobs
$122K - $131K
0% of jobs
$32K
$75.3K
$131K
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.
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.
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.

Full-time
Medical, Dental, Vision, Life, Retirement
Posted 19 days ago
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
Study Execution & Scientific Collaboration
Regulatory & Quality Oversight
Team Leadership
What We're Looking For:
Required Qualifications
Preferred Qualifications
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:
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.
Sourced by ZipRecruiter
Chemical manufacturing
10,000+ Employees
Waltham, MA, US