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Medical Safety Jobs (NOW HIRING)

Jj

Device Safety Officer

Raritan, NJ

Product Safety Job Sub Function: Product Safety Risk Management MD Job Category: Scientific ... Utilizing their medical / surgical training and deep domain expertise in device risk management ...

New

Johnson & Johnson

Device Safety Officer

Raritan, NJ · On-site

Product Safety Job Sub Function: Product Safety Risk Management MD Job Category: Scientific ... Utilizing their medical / surgical training and deep domain expertise in device risk management ...

New

BioNTech SE

Director Safety Physician

Cambridge, MA · On-site

$168K - $268K/yr

Pacific Northwest, US | full time | Job ID: 11471 About the role The Medical Safety Physician (MSP) plays a vital role in supporting the oncology therapeutic area by providing medical safety ...

Johnson & Johnson

Device Safety Officer

Horsham, PA

Product Safety Job Sub Function: Product Safety Risk Management MD Job Category: Scientific ... Utilizing their medical / surgical training and deep domain expertise in device risk management ...

New

Servier

Director, Global Safety Lead

Boston, MA · On-site

$250K - $300K/yr

Responsibilities include medical review, participation in drug safety related activities associated with clinical development, signal detection and evaluation, preparation of aggregate safety reports ...

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Medical Safety information

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$73K

$162.4K

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How much do medical safety jobs pay per year?

As of Jul 24, 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:
What job categories do people searching Medical Safety jobs look for? The top searched job categories for Medical Safety jobs are:
Medical Safety jobs near you
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 Director, Pharmacovigilance

Kailera Therapeutics, Inc.

Waltham, MA • On-site

Full-time

Medical, Life, Retirement

Posted 13 days ago

Job description

At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailera's mission to advance novel therapies for obesity and related conditions.
We are passionate about creating an inclusive workplace that promotes collaboration, integrity, and excellence. As we expand, we seek the most talented individuals with diverse backgrounds, cultures, perspectives, and experiences to join our team.
What You'll Do:
Reporting to the Senior Medical Director, Global Patient Safety and Pharmacovigilance (PSPV), the Medical Director will provide strategic, scientific, and tactical leadership for global medical safety evaluation and benefit-risk management for assigned Kailera products throughout their lifecycle with focus on patient well-being and compliance with applicable regulatory requirements.
This role is instrumental in ensuring patient safety, regulatory compliance, and robust characterization of benefit-risk in both clinical development and real-world use, including shaping risk-management strategies, integrated evidence generation planning, and real-world evidence approaches.
The medical director will collaborate extensively across and within their own function to advance Kailera's pharmacovigilance strategy to support the company's evolving pipeline, innovation, and mission.
Responsibilities:
  • Provide expert medical interpretation of safety data from all sources (clinical, post-marketing, literature, and RWE) and perform medical review of Individual Case Safety Reports (ICSR) within the ARGUS database
  • Oversee and execute safety signal detection and evaluation activities, ensuring timely, scientifically sound assessments and the optimization of signaling systems through data visualization and analysis tools
  • Incorporate insights from real-world data (EHRs, claims, registries) into surveillance and benefit-risk assessments to support evidence-generation strategies
  • Lead the development and oversight of global benefit-risk assessments and safety surveillance for clinical development programs and post-marketing phases
  • Drive the lifecycle management of Risk Management Plans (RMPs) and other risk minimization strategies, ensuring proactive identification and mitigation of safety risks
  • Lead the authoring and medical review of safety sections for regulatory documents (IBs, Protocols, DSURs, PSUR/PBRERs, and RMPs) and safety modules for marketing applications
  • Support labeling decisions and contribute medical expertise to safety communications, risk materials, and scientific publications
  • Collaborate with cross-functional stakeholders to integrate safety considerations into clinical development, post-marketing activities, and evidence-generation strategies
  • Lead and inspire a team of PSPV MDs, scientists, and operational colleagues, fostering a culture of accountability, scientific excellence, and collaboration
  • Partner with senior leadership (SVP/Medical Director) on departmental goals, organizational design, budgeting, and long-term pharmacovigilance planning
  • Act as a Subject Matter Expert (SME) for safety technology strategies, identifying innovative technical or resourcing solutions to improve DSPV surveillance capabilities
  • Contribute to the design, implementation, and enhancement of drug safety processes and systems to ensure high-performance PV operations
  • Maintain the medical safety governance framework, ensuring the timely identification, assessment, and escalation of significant safety issues
  • Represent the PSPV function during audits and inspections, leading the preparation of responses and managing deviations or CAPAs related to medical safety science.
  • Drive the development of SOPs, work instructions, and "fit-to-purpose" pharmacovigilance training for internal and external partners

Required Qualifications:
  • 8+ years of experience in global pharmacovigilance
  • 2+ years of experience in clinical practice or academic medicine
  • Proven experience in safety data analysis, signal management, and benefit-risk evaluation
  • Working knowledge of safety databases (Argus, ArisG/LifeSphere Safety, or similar)
  • Demonstrated ability to develop and implement drug safety strategies, risk management plans, and safety governance models
  • Proven experience with authoring or contributing to clinical study and regulatory submission documents
  • Thorough knowledge of relevant FDA and International Conference on Harmonization (ICH) guidelines, including Good Clinical Practices (GCP) guidelines
  • Strong knowledge of global safety and pharmacovigilance regulations, guidelines, and industry standards (FDA, EMA, ICH, GVP)
  • Experience in creating or managing working documents such as SOPs or Work Instructions
  • Strong ability to proactively identify risks and initiate/manage risk minimization activities
  • Strong ability to lead in a cross functional setting and work collaboratively with internal and external partners in a fast-paced environment
  • Strong ability to prioritize, multitask, and deliver quality results that meet tight timelines
  • Ability to influence and keep teams focused and motivated
  • Strong ability to communicate complex issues clearly

Preferred Qualifications:
  • Experience in pharmacoepidemiology, data science, or medical affairs is a plus

Education:
  • MD, DO or equivalent medical degree required. Ph.D. degree is a plus

Salary Range
$254,000-$305,000 USD
For Full Time Roles: This range represents the company's good-faith estimate of the salary at the time of posting. Actual pay may vary based on experience, skills, qualifications, location, and internal equity. We also offer comprehensive health coverage, flexible time off, paid holidays, and a year-end shutdown. Enjoy a monthly wellness stipend, generous 401(k) match, tuition reimbursement, commuter benefits, disability and life insurance, plus annual bonus opportunities and equity grants-because your well-being and future matter to us.
EQUAL EMPLOYMENT OPPORTUNITY INFORMATION:
Kailera Therapeutics, Inc. is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race (including traits historically associated with race, such as hair texture and protective hairstyles), color, creed, religion (including religious dress and grooming practices), national origin, ancestry, citizenship status, age (40 and over), sex or gender (including pregnancy, childbirth, pregnancy-related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, reproductive health decisions, domestic victim status, political affiliation, or any other characteristic protected by applicable federal, state, or local laws and ordinances.
E-Verify:
Kailera Therapeutics, Inc. uses E-Verify to confirm the identity and employment eligibility of all new hires.
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