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Fda Medical Officer Jobs (NOW HIRING)

Ctsnet, Inc.

Chief Medical Research Officer

Bethesda, MD · On-site

$150 - $200/hr

... Chief Medical Research Officer (CMROs) in one of three extramural divisions: Division of ... and FDA regulations and polices. * Experience in working with practitioners, patients and ...

New

Alston & Bird's

FDA Technical Consultant

Washington, DC · On-site

... and medical device manufacturing sites. This role offers flexibility to work hybrid or a fully ... Minimum of 5 years as an FDA investigator or compliance officer, or industry senior position in ...

Alston

FDA Technical Consultant

Washington, DC · On-site +1

... and medical device manufacturing sites. This role offers flexibility to work hybrid or a fully ... Minimum of 5 years as an FDA investigator or compliance officer, or industry senior position in ...

Insightsurgery

Head of US Engineering

Houston, TX · On-site

$200 - $250/hr

Reports to the Chief Operating Officer. Insight Surgeryhelps surgeons plan the most complex ... Working knowledge of FDA medical device requirements.Familiarity with UK regs is an advantage

OctaPharma Plasma

Medical Professional

Portland, OR

Medical Professional-EMT This Is Who You Are: * An individual of strong character and demonstrated ... FDA), Clinical Laboratory Improvement Act (CLIA), and cGMP. * May not fulfill Licensed Physician ...

Octapharma Plasma

Medical Professional

Portland, OR · On-site

Medical Professional-EMT This Is Who You Are: * An individual of strong character and demonstrated ... FDA), Clinical Laboratory Improvement Act (CLIA), and cGMP. * May not fulfill Licensed Physician ...

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FDA Medical Officer information

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$21K

$92.6K

$178K

How much do fda medical officer jobs pay per year?

As of Sep 8, 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 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 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 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.

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.

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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, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $92,555 per year, or $44.5 per hour.

Associate Director, Medical Affairs, West Coast

Taylor Strategy Partners

Portland, OR • On-site

$200K/yr

Full-time

Re-posted 13 hours ago

Job description

Description
TSP Talent Solutions has been retained by a global biopharmaceutical company specializing in severe orphan diseases to recruit an Associate Director, Medical Affairs - West Coast. This role will serve as a key liaison to the medical and scientific community, focusing on building and maintaining relationships with leading experts in pediatric neurology and epilepsy across the West Coast.
This position reports to the Medical Officer, North America within the North America subsidiary.
RESPONSIBILITIES:
  • Build, maintain, and manage professional relationships with Key External Experts (KEEs) to organize networks at state levels within their designated region
  • Ensure the appropriate dissemination of clinical and scientific information regarding marketed and pipeline compounds in a timely, ethical and health care provider (HCP)-focused manner
  • Implement clinical and educational strategies in collaboration with other company colleagues for designated HCPs/KEEs. This includes organizing medical and scientific training sessions, conferences and symposiums in medical centers and during scientific congresses in the US
  • Contribute to an efficient organization of medical communication activities for the marketed drug
  • Execute and support department projects as directed by the Medical Officer
  • Report pharmacovigilance (PV), product quality (PQ), or medical information (MI) requests within 24 hours, per the Standard Operating Procedures for PV, PQ, and MI reporting
  • Ensure competitive and scientific intelligence is communicated to medical and leadership team
  • Input all KEE/HCP interactions in company's software platform(s) in a timely manner. The minimum requirement is weekly input
  • Work to pair our KEE/HCP educational and research questions with the latest emerging data in response to specific healthcare professional inquiries

EXPANDED RESPONSIBILITIES INCLUDE BUT NOT LIMITED TO:
  • Providing clinical and value-based input into Biocodex communications and materials, as directed by Medical Officer
  • Medical Affairs Insights Lead with report generation
  • Specialty Pharmacy data generation and Medical Affairs liaison
  • Standard HCP (Health Care Provider) Response Letters: organization and updates
  • Recurring updates to Medical Affairs deck updates
  • Medical Affairs lead on Inpatient ordering program
  • Medical Affairs lead reviewer for PRC (promotional review committee) and MRC (medical review committee)
  • Expanded geography and key HCP responsibilities

QUALIFICATIONS:
  • Advanced scientific degree preferred (MD, PhD, PharmD), and will consider DNP, or clinically equivalent if appropriate experience (e.g., APRN, PA, RPh)
  • Minimum of 5 years of experience in the pharmaceutical industry (preferred) as a field-based medical position (MSL or similar) to provide strategic and scientific/medical direction to national/regional business unit functions
  • Preferred experience in rare disease; and/or neurology or pediatrics
  • Knowledge of FDA Regulations and Medical Affairs SOPs and Guidelines
  • Ability to respond appropriately to needs of key stakeholders and manage expectations; excellent project management skills and follow through
  • Excellent data analysis skills; strong understanding of clinical databases
  • Excellent verbal and written communication skills, and exceptional interpersonal skills
  • Ability to work under deadline in a fast-paced environment with a high degree of flexibility
  • Excellent problem-solving skills required
  • Ability to effectively facilitate meetings and cross-functional teams
  • Project management experience (timelines, documents, reporting) preferred

EDUCATION:
  • Advanced scientific or clinical degree preferred (MD, PharmD, PhD)

REQUIREMENTS - SKILLS, ABILITIES, AND TRAVEL:
  • A reliable team-player with strong organizational, project management, detail oriented, and communication skills
  • Proactive work style
  • Ability to be resilient, flex, and adapt to internal and external change
  • Work collaboratively across the organization
  • Autonomous and ability to work in fast-changing and multi-tasking environment
  • Ability to manage and communicate in a scientific and medical environment
  • Strong management and leadership capabilities
  • Excellent writing skills
  • A valid unrestricted driver's license
  • The US Field-Based position is associated with a minimum of 60% time in the field while customer facing

The anticipated base salary for this role is $200,000.

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