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Medical Safety Jobs (NOW HIRING)

Revolution Medicines

Safety Scientist

Redwood City, CA · Hybrid

Additional safety related activities will involve medical review of individual case safety reports (ICSRs), safety surveillance of assigned products and active member of cross-functional teams. The ...

Lancesoft

Director, Medical Reviewer

Cambridge, MA · On-site

$139.86 - $145/hr

Responsible for overseeing high quality medical assessment of individual case safety reports in the Global Safety Database to ensure compliance with domestic and international regulations. * Ensure ...

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How much do medical safety jobs pay per year?

As of Jun 11, 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 Safety Director or Chief Safety Officer typically have the highest salaries, often exceeding six figures annually. These positions require extensive experience, certifications like RAC or CSP, and oversight of safety protocols across organizations.

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 can you 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 manager. These positions involve developing safety protocols, conducting risk assessments, and ensuring compliance with regulations in various industries, often requiring certifications like OSHA or NEBOSH.

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 and promotes a culture of safety within healthcare facilities.

What does a health and safety specialist do?

A health and safety specialist is responsible for developing, implementing, and monitoring safety protocols to ensure a safe work environment. They conduct inspections, investigate accidents, and ensure compliance with regulations such as OSHA, often requiring certifications like CSP or CIH. Their work involves risk assessment, training employees, and maintaining safety records.
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 June 2026, with employment types broken down into 1% As Needed, 79% Full Time, 19% Part Time, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $162,390 per year, or $78.1 per hour.
Global Safety Program Lead/Sr Medical Director

Global Safety Program Lead/Sr Medical Director

AstraZeneca

Boston, MA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 14 days ago

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 71 rated pharmaceutical

Job description

This is what you will do:
The Global Safety Program Lead, Senior Director is accountable to the Global Safety Head for the safety strategy, delivery, and oversight of the assigned asset(s); the professional will work with safety physicians and scientists responsible for the development, implementation, and application of safety strategy at asset and study level. Acts strategically to generate opportunity and value for the asset or indication to optimize benefit risk and maintain a competitive advantage. Line manages a team of safety physicians and / or scientists. They will be required at times to deputise for the Global Safety Head.
The Global Safety Program Lead, Senior Director will operate according to the highest ethical, quality and compliance standards in compliance as provided by global and local regulations, GxP practice and AZ procedures.
You will be responsible for:
Safety Expert
  • Accountable for the overall scientific and clinical safety content for the assigned asset(s) or indications.
  • Accountable for the implementation and the high quality delivery of the Safety & Strategy Management Team (SSaMT) and Safety Surveillance Team for assigned asset(s).
  • Responsible for overall safety content for the product or indication(s) aligned to GPT strategy. Sets safety team goals aligned to TA and product strategy.
  • For the assigned asset(s), accountable for safety TPP, Safety Go/No Go criteria, safety communication/messaging and the guidelines for toxicity management of the asset
  • Is accountable for project representation for Global Patient Safety at governance and other forums where safety is involved, eg DRC, eCRC, SARB, FSIRB, and DSMB/DMC, Medical Affairs Review Committees (MARC), product teams such CPT and GPT and Advisory Board meetings in partnership with GSH.
  • Accountable for the quality of key safety deliverables e.g., Risk Management Plans (RMPs) and Periodic Safety Reports (PSRs), compliance and adherence to PV regulations of the assigned asset(s).
  • Leads response to complex technical issues for specific safety aspects for the assigned asset(s).
  • Is accountable for safety contribution to study designs and study concept delivery within their assigned program
  • Through integrated understanding of the product strategy, provides strategic safety knowledge and support to the safety medical directors and scientists through initiation, execution, and completion of the clinical programs for the assigned asset(s).
  • Leads the safety physicians and scientists to support the safety strategy and input into the program design, monitoring, and data interpretation from pre-clinical and clinical studies, communication and post-marketing surveillance, epidemiology, pre-clinical and literature, epidemiology for each asset.
  • Ensures that own work and work of team is compliant with Safety Health and Environment (SHE) standards and all other relevant internal and external regulations and standards.
  • Represents the Company and accountable for the quality of safety delivery e.g., regulatory submissions, answers to Health Authority Queries, Ethic Committees, Marketing Companies, investigators/sites, and provides clarifications as well as solves safety issues in the study team.
  • May be required to support in-licensing opportunities.

  • Promotes and enables cross-functional, proactive and solutions-orientated team actions and behaviours
  • Accountable for implementation of new processes, systems and learning, including new ways of working.
  • Prioritizes risk mitigation strategies and effective trouble shooting.
  • Line manages a team of safety physicians and / or scientists.

Scientific clinical safety analytical accountabilities
  • Maintains up-to-date knowledge of the relevant safety scientific literature, and is able to clearly communicate key impactful information,
  • Accountable for proper data collection and interpretation for determination of the risks and inform the label in markets globally
  • Delivers analyses of clinical safety data in a balanced and statistically robust manner, to drive interpretations and develop novel proposals.
  • Serves as a source of scientific and clinical safety knowledge for the Product Team, in the analyses and interpretation of scientific and clinical safety data.

You will need to have:
  • Medical degree or equivalent degree in biomedicine or science
  • 5 years extensive relevant clinical, safety and risk management experience in the pharmaceutical, biotech, CRO industry, academia or Health Authorities
  • Proven track record of successful clinical safety delivery with demonstrated examples of strategic influence to clinical studies/programs.
  • Ability to collaborate across a matrixed environment and influence cross-functional- leaders on decision-making (e.g. Clinical Development, Medical Affairs, Regulatory Affairs).
  • Thorough knowledge and understanding of pharmacovigilance & safety deliverables, standards and processes at a global level; including pre and post launch experience.
  • Experience of global regulatory submissions and interacting with major regulatory agencies.
  • Demonstrated ability to successfully lead, coach, and mentor other safety medical directors/scientists.
  • Available to travel domestically and internationally
  • Demonstrated ability to present complex topics to senior leaders at safety and development governances for alignment and endorsement.

We would prefer for you to have:
  • PhD (or other complementary degree) in scientific discipline.
  • Excellent, independent judgment based on leading-edge knowledge and expertise.
  • Excellent speaking skills, industry conference speaking experience.
  • Excellent, independent judgment based on knowledge and expertise.
  • Demonstrated clinical safety and research expertise in an appropriate disease area.

The annual base pay (or hourly rate of compensation) for this position ranges from $280,895 to $421,342. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Date Posted
26-May-2026
Closing Date
29-Jun-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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