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Fda Investigator Jobs in Michigan (NOW HIRING)

Civia Health

Principal Investigator, MD

Shelby, MI · On-site

Ensure compliance with all ICH-GCP, FDA, and IRB regulations. * Provide guidance and mentorship to ... Principal Investigator in clinical research (Phase 2-4 preferred). * Board certification in ...

Civia health

Principal Investigator, MD

Utica, MI · On-site

Ensure compliance with all ICH-GCP, FDA, and IRB regulations. * Provide guidance and mentorship to ... Principal Investigator in clinical research (Phase 2-4 preferred). * Board certification in ...

Mitovation

Be Seen First

Systems Engineer - Medical Device Company

Ann Arbor, MI · On-site

$110K - $140K/yr

The technology originated from mitochondrial biology research at Wayne State University and the University of Michigan and has progressed through an active FDA Investigational Device Exemption (IDE ...

AA2IT

Quality Specialist

Wyandotte, MI · On-site

$26/hr

Provide FDA with NCM review, as needed. * Work with EHS Management Systems (Responsible Care ... investigators and work with Legal to develop customer letter for product quality NCMS as ...

AA2IT

Quality Specialist

Wyandotte, MI · On-site

$26/hr

Provide FDA with NCM review, as needed. * Work with EHS Management Systems (Responsible Care ... investigators and work with Legal to develop customer letter for product quality NCMS as ...

DM Clinical

Study Manager I (4187)

Bay City, MI · On-site

A Study Manager I is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to ...

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All JobsFda Investigator JobsFda Investigator Jobs in Michigan

Fda Investigator information

See Michigan salary details

$27.9K

$65.7K

$114.2K

How much do fda investigator jobs pay per year?

As of Sep 6, 2026, the average yearly pay for fda investigator in Michigan is $65,652.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,800.00 and $85,900.00 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 Michigan?

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

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

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

Fda Investigator jobs near you
Infographic showing various Fda Investigator job openings in Michigan as of August 2026, with employment types broken down into 84% Full Time, and 16% Part Time. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $65,652 per year, or $31.6 per hour.

Principal Investigator, MD

Civia Health

Shelby, MI • On-site

Full-time

Medical, Dental, Vision, PTO

Re-posted 24 days ago

Key responsibilities

  • Serve as the physician of record and lead clinical oversight for assigned trials.

  • Review and approve study protocols, informed consent documents, and source documentation.

  • Conduct physical exams, medical reviews, and oversee safety assessments for participants.

Job description

Reports to: Medical Director
Join Us at Civia Health
At Civia Health, we're reimagining how clinical trials are delivered-by putting patients first and empowering providers to lead innovation. We're seeking an experienced and compassionate Principal Investigator (PI) to oversee Phase 2-4 clinical trials in a collaborative, mission-driven environment. You'll play a vital role in ensuring scientific integrity, patient safety, and regulatory compliance while contributing to groundbreaking research.
At Civia Health, you're not just taking a job: You're joining a mission to transform the way clinical research is done. Our purpose is bold: to bring clinical trials front and center in your community, make them accessible to everyday people, and empower underrepresented communities to participate.
We're reinventing how clinical studies are run, delivering valid, scalable evidence with a consumer-first mindset. Too often, trials are expensive, fragmented, and overlook the experience of the participant. At Civia, we're changing that. Our leadership team are experienced industry leading, visionary professionals who know what's broken - and how to fix it.
We treat participants like valued partners, not research subjects. That means supporting their agency, putting their needs, comfort, and enjoyment first - and rewarding them generously for their time and effort.
What It Means to Work at Civia
Every team member plays a crucial role in reshaping clinical research. You'll help make studies more human-centered, inclusive, and efficient. We're looking for people who are driven by purpose, inspired by innovation, and ready to roll up their sleeves to do meaningful work.
At Civia, your contributions aren't just transactional, they're transformational.
What You'll Do
  • Serve as the physician of record and lead clinical oversight for assigned trials.
  • Review and approve study protocols, informed consent documents, and source documentation.
  • Conduct physical exams, medical reviews, and oversee safety assessments for participants.
  • Ensure compliance with all ICH-GCP, FDA, and IRB regulations.
  • Provide guidance and mentorship to the clinical research team.
  • Engage with sponsors, monitors, and regulatory bodies as needed.
  • Occasional travel may be required for audits, site visits, or team meetings.

What You Bring
  • Medical degree (MD or DO) with active and unrestricted license.
  • 3+ years of experience as a Principal Investigator in clinical research (Phase 2-4 preferred).
  • Board certification in internal medicine, endocrinology, or related field preferred.
  • Strong working knowledge of GCP, FDA regulations, and clinical operations.
  • Excellent leadership, communication, and problem-solving skills.
  • Passion for innovation, ethics, and patient-centered care.

What We Offer
  • Competitive compensation
  • Medical, dental, and vision insurance
  • Generous PTO and paid holidays
  • Flexible scheduling options
  • Professional development and continuing education support
  • A mission-driven team that values respect, inclusion, and innovation

Ready to Make an Impact?
  • Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact.
  • Startup Energy, Proven Expertise: Work fast, adapt quickly, and help build something new; guided by seasoned visionaryprofessionals who've seen what needs to change.
  • People First Culture: We care deeply about our patients, participants, and each other. Collaboration, transparency, and bold, straight-talking are core to how we work.
  • Invested in Your Growth: We don't just hire for today; we're building the leaders and changemakers of tomorrow.

If you're ready to be part of something meaningful-and work with people who care deeply about doing good work-apply today by submitting your resume and cover letter to the link above. We're excited to learn more about you!

Apply