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Fda Medical Officer Jobs (NOW HIRING)

Emmes

Senior Medical Officer

Rockville, MD · On-site +1

Overview Sr Medical Officer US Remote Emmes Group: Building a better future for us all. Emmes Group ... Reviews the FDA MedWatch Alerts, safety communications and or other communications from other ...

Kids for the Future

Chief Medical Officer

Chapel Hill, NC · On-site

$288 - $352/hr

Chief Medical Officer (CMO) Reporting to: President Location : Strong preference for Chapel Hill ... Stay abreast of the evolving regulatory landscape (including FDA digital health guidance and FTC ...

Well

Chief Medical Officer

Chapel Hill, NC · On-site

$320K/yr

Chief Medical Officer (CMO) Reporting to: President Location: Strong preference for Chapel Hill, NC ... Stay abreast of the evolving regulatory landscape (including FDA digital health guidance and FTC ...

insitro

Chief Medical Officer

South San Francisco, CA · On-site

We are seeking an innovative, highly quantitative, and data-driven Chief Medical Officer (CMO) to ... Lead successful interactions and submissions with major global regulatory bodies (e.g., FDA, EMA ...

Guidehouse

Senior Medical Officer

Rockville, MD · On-site

$85K - $141K/yr

We are looking for a Senior Medical Officer to support the National Institute of Allergy and ... Prior experience interacting with FDA or other regulatory agencies. * Previous service on clinical ...

Guidehouse

Senior Medical Officer

Rockville, MD

$85K - $141K/yr

We are looking for a Senior Medical Officer to support the National Institute of Allergy and ... Prior experience interacting with FDA or other regulatory agencies. * Previous service on clinical ...

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All JobsFda Medical Officer Jobs

FDA Medical Officer information

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$21K

$92.6K

$178K

How much do fda medical officer jobs pay per year?

As of Aug 15, 2026, the average yearly pay for fda medical officer in the United States is $92,555.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,500.00 and $84,500.00 per year, depending on experience, location, and employer.

What does an FDA Medical Officer do?

As an FDA Medical Officer, your typical day involves reviewing clinical trial data, evaluating the safety and efficacy of medical products, and preparing scientific assessments for regulatory decisions. You will often collaborate closely with multidisciplinary teams, including scientists, statisticians, and regulatory specialists, to ensure thorough analysis and compliance with federal regulations. The work environment is fast-paced, requiring strong analytical and communication skills, as you may also participate in meetings with external stakeholders, such as pharmaceutical companies or advisory committees. This role provides continuous learning opportunities and can lead to career growth within the agency, such as leadership or policy development positions.

What is the difference between Fda Medical Officer vs Fda Reviewer?

AspectFda Medical OfficerFda Reviewer
Required CredentialsMedical degree (MD), license, often board certificationMedical or scientific background, often with advanced degrees
Work EnvironmentRegulatory agencies, hospitals, or government officesReviewing applications, clinical data, and labeling
Employer & IndustryU.S. Food and Drug Administration, healthcare, pharmaceuticalsFDA, pharmaceutical companies, biotech firms

Fda Medical Officers and Fda Reviewers both work within the FDA, but Medical Officers typically oversee clinical and safety aspects of medical products, while Reviewers focus on evaluating data and labeling for approval. Both roles require medical expertise and are essential in the regulatory process, but they differ in daily responsibilities and focus areas.

What is an FDA Medical Officer?

FDA Medical Officers are licensed physicians who work for the U.S. Food and Drug Administration (FDA). Their primary role is to evaluate and review data from clinical trials and scientific studies to ensure that drugs, biologics, and medical devices are safe and effective for public use. They provide medical expertise during the regulatory review process and help develop policies and guidelines related to public health. FDA Medical Officers also collaborate with scientists, industry representatives, and other government agencies to protect and promote public health.

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

To thrive as an FDA Medical Officer, you need a medical degree (MD or DO), clinical experience, and a thorough understanding of regulatory science and public health. Familiarity with FDA regulatory databases, submission review systems, and relevant certifications in clinical research or regulatory affairs are commonly required. Strong analytical thinking, attention to detail, and effective communication skills help distinguish top performers in this role. These skills ensure that medical products are rigorously evaluated for safety and efficacy, upholding public health standards and regulatory compliance.
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FDA Medical Officer jobs near you
Infographic showing various Fda Medical Officer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $92,555 per year, or $44.5 per hour.

Surgical Oncologist - FDA

Tunnell Government Services

Bethesda, MD

Full-time

Re-posted 3 days ago

Job description

FDA CDRH - Medical Officer (Surgical Oncologist) SME Position Description 

The mission of the FDA Center for Devices and Radiological Health (CDRH) is to protect and promote the public health. CDRH assures that patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products.

Tunnell Government Services, Inc. is providing professional and scientific services to the CDRH with expert consultants with scientific expertise in the regulation and approval and of medical devices. In general, these consultants provide consultation related to supporting medical device reviews (EUA, 510(k), PME and De Novo marketing applications, Pre-submissions); participate in meetings and teleconferences; coordinate meetings with internal and external stakeholders; develop written reviews and correspondence; perform research; conduct data analysis; write detailed documents and reports; and execute other administrative office tasks related to CDRH's projects.

Tunnell is seeking a candidate to provide expert consulting services to assist the CDRH with their regulatory responsibilities. This candidate should possess specific expertise and training in surgical oncology, as relevant to medical devices.

Requirements and Qualifications

  • The candidate must possess a Doctor of Medicine (M.D. or equivalent) from an accredited medical school in the United States.
  • In addition, the candidate must possess a current, active, full, and unrestricted medical license or registration as a Physician to practice medicine in a State, District of Columbia, the Commonwealth of Puerto Rico, or a territory of the United States.
  • At least ten (10) years of relevant clinical experience
  • Certification from a U.S. relevant specialty board organization, e.g., the American Board of Surgery (ABS), Society of Surgical Oncology (SSO), etc.  
  • Thorough understanding of current clinical practices in surgical oncology, including diagnosis and treatment, and current/emerging trends in practice.
  • Expert in function and utilization of medical devices commonly used as part of surgical oncology (e.g., advanced energy and resection devices [electrosurgical units, ultrasonic scalpels, argon beam coagulators], minimally invasive and robotic platforms [robotic-assisted surgery systems, laparoscopes and thoracoscopes], localization and navigation devices [tumor localization seeds, intraoperative ultrasound], tumor ablation systems [radiofrequency ablation and microwave ablation, cryoablation systems, irreversible electroporation], lymph node mapping systems [gamma probes, near-infrared fluorescence imaging], intraoperative therapy devices [hyperthermic intraperitoneal chemotherapy pumps, intraoperative radiation therapy systems]).
  • Familiarity with relevant FDA medical device regulatory processes, regulations (e.g., 21 CFR Part 878 - General and Plastic Surgery Devices), and guidances is preferred.
  • Ability to communicate well with others using excellent written and verbal communication skills.
  • Excellent interpersonal skills, with the ability to effectively work both independently and within a team of technical personnel.

This position is 100% telework. 

Must be a US Citizen or a Full Green Card holder.

Apply