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Medical Safety Manager Jobs (NOW HIRING)

The Medical Safety Lead provides strategic medical safety leadership, serving as the single point ... Lead and contribute to the safety signal management and benefit risk assessment activities as well ...

Product Safety Risk Management MD Job Category: Scientific/Technology All Job Posting Locations: Irvine, California, United States of America JOB POSITION SUMMARY: * The MSO role will provide medical ...

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How much do medical safety manager jobs pay per year?

As of Jun 11, 2026, the average yearly pay for medical safety manager in the United States is $98,189.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $116,500.00 per year, depending on experience, location, and employer.

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

To thrive as a Medical Safety Manager, you need a strong background in pharmacovigilance, clinical research, and regulatory compliance, often supported by a degree in pharmacy, medicine, or life sciences. Familiarity with safety databases (such as Argus or ARISg), MedDRA coding, and global regulatory reporting systems is essential. Excellent analytical thinking, attention to detail, and effective communication skills set outstanding professionals apart in this field. These skills and qualities are crucial for ensuring drug safety, regulatory adherence, and protecting patient well-being throughout clinical development and post-marketing surveillance.

How does a Medical Safety Manager typically collaborate with cross-functional teams during the drug development process?

Medical Safety Managers play a central role in ensuring patient safety by working closely with teams such as clinical research, regulatory affairs, pharmacovigilance, and medical affairs. They regularly participate in multidisciplinary meetings to review safety data, assess risk, and implement mitigation strategies. Their collaboration ensures that safety concerns are addressed promptly and that regulatory submissions reflect the most up-to-date safety profiles. Effective communication and coordination with these teams are essential for successful product development and compliance with industry standards.

What does a Medical Safety Manager do?

A Medical Safety Manager is responsible for overseeing the safety of pharmaceutical products throughout their lifecycle. They analyze and evaluate data related to adverse drug reactions, ensure compliance with regulatory requirements, and implement risk management strategies. Medical Safety Managers work closely with clinical teams, regulatory authorities, and healthcare professionals to monitor, assess, and report on drug safety. Their work is critical in ensuring that medicines are safe for patients and that any potential risks are identified and managed appropriately.

Is an EHS manager a stressful job?

A Medical Safety Manager role can be stressful due to the responsibility of ensuring compliance with safety regulations, managing risk assessments, and responding to safety incidents. The job often requires attention to detail, strong communication skills, and the ability to handle urgent situations, which can contribute to workplace stress.

How much do EHS managers make?

EHS (Environmental, Health, and Safety) managers in Wisconsin typically earn between $80,000 and $110,000 annually, depending on experience, industry, and certifications such as CSP or OSHA training. Salaries for Medical Safety Managers, a related role, generally fall within this range or higher with specialized expertise and leadership responsibilities.

What is the highest paying safety position?

In the field of safety management, senior roles such as Director of Safety or Vice President of Safety typically have the highest salaries, often exceeding $150,000 annually. These positions require extensive experience, advanced certifications like CSP or ASP, and leadership skills, and they oversee safety programs at organizational or corporate levels.

Do you need a degree to be an EHS manager?

A degree is often preferred for a Medical Safety Manager or EHS (Environmental, Health, and Safety) manager role, but relevant experience, certifications, and knowledge of safety regulations can also be sufficient. Many employers value industry-specific certifications like OSHA or NEBOSH alongside practical experience. Educational requirements vary by company and position level.

What is the difference between Medical Safety Manager vs Medical Safety Specialist?

AspectMedical Safety ManagerMedical Safety Specialist
CertificationsMedical Safety Certification, Pharmacovigilance trainingMedical Safety Certification, Pharmacovigilance training
Work EnvironmentLeads safety teams, manages safety programsSupports safety activities, conducts case assessments
Employer & Industry UsagePharmaceutical companies, biotech firmsPharmaceutical companies, clinical research organizations

The Medical Safety Manager and Medical Safety Specialist roles share similar certifications and work environments within the pharmaceutical industry. The manager oversees safety programs and teams, while the specialist focuses on case assessments and support tasks. Both roles are essential for ensuring drug safety and compliance.

What cities are hiring for Medical Safety Manager jobs? Cities with the most Medical Safety Manager 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 Manager jobs? States with the most job openings for Medical Safety Manager jobs include:
Infographic showing various Medical Safety Manager job openings in the United States as of June 2026, with employment types broken down into 84% Full Time, 8% Part Time, and 8% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $98,189 per year, or $47.2 per hour.

Director, Medical Safety Scientist

Jazz Pharmaceutical

Philadelphia, PA • Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago


Job description

If you are a current Jazz employee please apply via the Internal Career site

Jazz Pharmaceuticalsis a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered inDublin, Irelandwith research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visitwww.jazzpharmaceuticals.comfor more information.

Job Description

The Director, Medical Safety (Scientist) is a key member of the Medical Safety team, and provides leadership, line management, and/or mentorship for the junior safety scientists within Medical Safety organization. In close collaboration with Medical Safety Physician and/or Medical Safety Scientist line manager, this role leads, oversees and coordinates all Medical Safety activities for respective TA/ product franchise as well as Medical Safety organization as a whole. This role is responsible for ensuring up to date processes / procedures for safety governance, signal management, clinical surveillance, periodic safety reporting, and risk management and/or driving innovation initiatives within Medical Safety organization. In close collaboration with Medical Safety Physician, this role is also responsible for contributing to regulatory submission safety strategy. Other responsibilities include but are not limited to: signal management activities, production of aggregate safety reports (e.g., DSURs, PADERs, PBRERs), provision of high-level scientific expertise in the safety evaluation and risk management strategies of assigned products (e.g, signal evaluation reports, health hazard evaluations, and RMPs), global leadership / representation of Medical Safety within the company (e.g., leading Safety Management Teams, presenting at Executive Safety Board meetings), and SME support for HA inspections.

Essential Functions

Leads cross-functional safety management teams (SMTs) and drives safety strategy for responsible product/program.

Ensures that processes and procedures are up to date to meet regulatory requirements and inspection readiness

Drives signal management process using available methodologies, including making recommendations for the assessment and prioritization of safety concerns.

Effectively communicates with members of the interdisciplinary team regarding ongoing signal evaluation.

Ensures that available safety information is evaluated in order to meet both internal and external requirements, including identifying the need for labeling updates. Produces accurate and fit for purpose evaluation documents with clear conclusions, as required.

Leads the coordination of aggregate safety reports (PBRERs, DSURs, PADERs) and authors relevant sections, as appropriate.

Authors or provides guidance for the production of risk management plans (RMPs).

Provides strategic input into regulatory requests / responses.

Delivers clinical safety input into clinical development program.

Leads the medical safety contributions of global regulatory submissions for new products, formulations or indications.

Participate in and/or lead internal safety surveillance meetings as well as joint safety meetings with licensing

Partners, as needed.

Provides medical safety input into creation / review of Safety Data Exchange Agreements and/or other PV agreements.

Escalates issues / concerns to senior management in a timely and appropriate manner.

Mentors and trains junior members of the Medical Safety team.

Required Knowledge, Skills, and Abilities

Minimum Requirements

At least 8 years of experience in drug safety, including at least 5 years of experience in surveillance / risk management.

Ability to independently search clinical safety and literature databases for relevant information.

Expert knowledge of pharmacovigilance regulations regarding aggregate safety reports, risk management plans, and signal management.

Excellent medical writing skills, as well as proven ability to effectively lead interdisciplinary teams.

In-depth knowledge of medical and drug terminology, as well as the clinical development process.

Familiarity with MedDRA and safety databases; Proficient with Windows applications, and ability to learn new programs / databases.

Required/Preferred Education and Licenses

  • Requires a degree (e.g., BS, BA, MSc or PhD) or professional qualification in a life science field (e.g., nursing or pharmacy) or a relevant scientific/technical discipline.

#LI-Remote

Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.

The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits