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Medical Safety Jobs (NOW HIRING)

Company Description Medical Safety Physician 6-month assignment 100% Remote What are the three most important qualifications: Argus experience, self starter, experience in pharmacovigilance and ...

Medical Safety Engineer

Boxborough, MA · On-site

$68K - $85K/yr

Engineer-Medical Safety - Boxborough, Massachusetts Intertek, a leading provider of quality and safety solutions to many of the world's top-recognized brands and companies, is actively seeking an ...

Job TitleMedical Safety Manager - Ultrasound Medical Safety Manager, Ultrasound The Medical Safety Manager independently oversees safety surveillance activities for medical products by analyzing data ...

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Medical Safety information

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$73K

$162.4K

$246K

How much do medical safety jobs pay per year?

As of Jul 22, 2026, the average yearly pay for medical safety in the United States is $162,390.00, according to ZipRecruiter salary data. Most workers in this role earn between $100,000.00 and $207,000.00 per year, depending on experience, location, and employer.

What is the highest paying safety job?

In the field of medical safety, senior roles such as Medical Safety Director or Vice President of Safety typically have the highest salaries, often exceeding $150,000 annually. These positions require extensive experience, leadership skills, and often involve overseeing safety protocols and compliance in pharmaceutical or healthcare companies.

How long does it take to become a safety specialist?

Becoming a medical safety specialist typically requires a bachelor's degree in health, safety, or a related field, which takes about four years. Gaining relevant experience and obtaining certifications such as the Certified Safety Professional (CSP) can take additional years, with many professionals reaching full competency within 2-5 years after entering the field.

What can I do with a health and safety degree?

A health and safety degree prepares individuals for roles such as health and safety officer, environmental health specialist, or safety coordinator. These positions involve developing safety protocols, conducting risk assessments, and ensuring compliance with regulations, often requiring certifications like OSHA or NEBOSH. Graduates can work in industries such as manufacturing, construction, healthcare, or government agencies.

How does a Medical Safety professional typically collaborate with cross-functional teams in the pharmaceutical industry?

Medical Safety professionals work closely with colleagues in clinical research, regulatory affairs, medical affairs, and data management to ensure patient safety throughout the drug development process. They participate in safety review meetings, analyze adverse event data, and provide input on risk mitigation strategies. Effective communication and teamwork are essential, as Medical Safety specialists often translate complex safety data into actionable insights for both scientific and regulatory audiences.

What is the difference between Medical Safety vs Medical Compliance?

AspectMedical SafetyMedical Compliance
Required CredentialsCertifications in safety management, healthcare regulationsCertifications in healthcare laws, regulatory standards
Work EnvironmentHospitals, pharmaceutical companies, clinical settingsHealthcare facilities, regulatory agencies, pharmaceutical firms
Employer & Industry UsageFocuses on patient and staff safety protocolsEnsures adherence to legal and regulatory standards

Medical Safety and Medical Compliance roles often overlap but serve different focuses. Medical Safety emphasizes preventing hazards and ensuring safety protocols, while Medical Compliance centers on adhering to laws and regulations. Both are vital in healthcare settings, but their primary goals and certifications differ slightly.

What is medical safety and what do professionals in this field do?

Medical safety, often referred to as drug safety or pharmacovigilance, is a field focused on identifying, assessing, and preventing adverse effects or any other drug-related problems in patients. Professionals in medical safety monitor the safety profiles of pharmaceuticals and medical devices throughout their lifecycle, analyze data from clinical trials and real-world use, and report findings to regulatory authorities. Their work helps ensure that medications and treatments are both safe and effective for patients, and they play a key role in risk management and compliance with regulatory standards.

What are the key skills and qualifications needed to thrive as a Medical Safety professional, and why are they important?

To thrive as a Medical Safety professional, you need a strong background in life sciences, pharmacovigilance, regulatory compliance, and typically a degree in pharmacy, medicine, or a related field. Familiarity with safety databases (such as Argus or ARISg), signal detection systems, and relevant certifications like Drug Safety or Pharmacovigilance are often required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for this position. These skills ensure accurate assessment and reporting of adverse events, regulatory adherence, and ultimately, patient safety.

What does a safety officer do in healthcare?

A safety officer in healthcare is responsible for developing, implementing, and monitoring safety protocols to ensure a safe environment for patients and staff. They conduct risk assessments, investigate incidents, and ensure compliance with health and safety regulations, often requiring certifications like OSHA training. Their role helps prevent accidents, injuries, and exposure to hazards within healthcare facilities.
More about Medical Safety jobs
What cities are hiring for Medical Safety jobs? Cities with the most Medical Safety job openings:
What are the most commonly searched types of Medical Safety jobs? The most popular types of Medical Safety jobs are:
What states have the most Medical Safety jobs? States with the most job openings for Medical Safety jobs include:
Infographic showing various Medical Safety job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 78% Full Time, 14% Part Time, and 7% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $162,390 per year, or $78.1 per hour.

Medical Safety Physician

Spectra force

Lincolnton, NC • On-site, Remote

Contractor

Posted 10 days ago


Job description

Company Description
Job Description
Medical Safety Physician
6-month assignment
100% Remote
What are the three most important qualifications: Argus experience, self starter, experience in pharmacovigilance and infection disease vaccines
Licenses/Certifications: A Valid medical license (active or inactive), or equivalent, from the country or region in which he/she resides and works
Description
Delivers medical, clinical and scientific advisory expertise in clinical research studies and post marketing programs (RWI). Signal detection and aggregated reporting.
Provides medical, scientific and therapeutic expertise on pharmacovigilance services.
Participates in all aspects of the Medical Safety activities as per scope of work, such as performing medical review and clarification of trial-related Adverse Events including review of analysis of similar events, medical evaluation of post-marketing adverse drug reactions, review medical inputs for into signal management and benefit-risk evaluation of drugs in clinical trial and post marketing set up, safety aggregate report review, safety review of study protocol, investigators brochure and other reference safety information, clinical study report narrative review, providing medical assessment comments etc. and serving as an internal consultant for any medical support for pharmacovigilance operations.
Responsibilities
Essential Functions
• Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary
• Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements
• Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported
• Provide aggregate reviews of safety information, including clinical data, to maintain oversight of a product's safety profile
• Provide coding review of AEs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data
• Represent safety and clinical data review findings during client meetings
• Provide medical review and edits to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports
• Provide medical review and edits of Development Risk Management Plans, EU Risk Management Plans or US Risk
Evaluation and Mitigation Strategies
• Provide medical oversight for label development, review and change
• Provide medical support and attendance at Data Safety Monitoring Board Meetings
• Attends and contributes medical safety evaluation on Safety Monitoring Committees
• Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document
• Provide medical review and edits to Drug Safety Reports or other benefit-risk assessments
• Review and sign off on both the Project Safety Plan and the Medical Monitoring Plan per medical safety scope agreed in contract
• Perform Medical Safety review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs) for appropriate safety content and data capture.
• Act as Global Safety Physician or Assistant or Back-up on projects as assigned
• Attend project meetings, medical safety team meetings, and client meetings as requested
• Ensure coverage for all medical safety deliverables within regulatory or contracted timelines
• Provide medical escalation support for medical information projects
• Provide medical escalation support for EU Qualified Persons for Pharmacovigilance projects
• 24 hour medical support as required on assigned projects
• Maintain awareness of medical-safety-regulatory industry developments
Experience
Typically requires 5 - 7 years of prior relevant experience.
Knowledge
Requires deep knowledge of one or more related job areas typically obtained through advanced education combined with experience.
Typically viewed as having a specialty within discipline.
Education: A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
Skills & Abilities:
• Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including
• knowledge of regulations and guidelines pertaining to safety and good clinical practice
• Knowledge of clinical trials and pharmaceutical research process
• Ability to establish and meet priorities, deadlines, and objectives.
• Skills in providing consultation and advice on multiple assignments required, as well as initiative and flexibility
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
Physical Demands:
Sit at a desk or table with some walking, standing, bending, stooping, or carrying of light objects.
Perform continuous operation of a personal computer for four hours or more.
Use hands and fingers to handle and manipulate objects and/or operate equipment.
Qualifications
Additional Information
All your information will be kept confidential according to EEO guidelines.