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Safety Scientist Jobs (NOW HIRING)

Argenx

Safety Scientist

The Safety Scientist is responsible for the ongoing safety surveillance of assigned investigational and/or marketed products. The safety scientist directs a cross functional team comprised of and ...

Viridian Therapeutics, Inc.

Safety Scientist

Waltham, MA · On-site +1

$127K - $155K/yr

The Safety Scientist collaborates primarily with the Product Safety Lead/Safety Physician for assigned products, and also with cross-functional team members to ensure active safety surveillance of ...

BeiGene, Inc.

Director, Safety Scientist

The Director, Safety Scientist supports assigned compounds in conjunction with Product Safety Leads (PSLs) and leverages clinical and scientific expertise to lead the detection of safety signals ...

AstraZeneca

Director, Safety Scientist

Boston, MA · On-site

$175K - $263K/yr

The Director, Safety Scientist plays a leadership role within Global Patient Safety organizing and mentoring safety scientists to actively evaluate, manage and strategize risk in collaboration with ...

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How much do safety scientist jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for safety scientist in the United States is $61.42, according to ZipRecruiter salary data. Most workers in this role earn between $42.55 and $73.80 per hour, depending on experience, location, and employer.

How does a safety scientist typically collaborate with other departments to ensure drug safety throughout a product's lifecycle?

A Safety Scientist works closely with clinical development, regulatory affairs, and medical teams to monitor and assess the safety profile of pharmaceutical products. They regularly participate in cross-functional meetings, review safety data from clinical trials or post-marketing sources, and communicate findings to internal and external stakeholders. This collaborative approach ensures that potential risks are identified early and that appropriate risk mitigation strategies are implemented and documented throughout the product's lifecycle.

What is a safety scientist?

Safety Scientists are professionals who monitor, assess, and manage the safety of pharmaceuticals, medical devices, or other products to ensure they do not pose undue risks to patients or consumers. They analyze data from clinical trials, post-marketing reports, and scientific literature to identify potential safety concerns. Additionally, Safety Scientists help develop risk management strategies and communicate findings to regulatory authorities and stakeholders.

What are the key skills and qualifications needed to thrive as a safety scientist?

To thrive as a Safety Scientist, you need a strong background in pharmacovigilance, drug safety regulations, and data analysis, typically supported by a degree in life sciences or a related field. Familiarity with safety databases (such as Argus or ARISg), signal detection tools, and compliance standards like GVP or FDA regulations is crucial. Strong attention to detail, analytical thinking, and effective communication are essential soft skills for assessing risks and collaborating with cross-functional teams. These skills ensure accurate safety assessments, regulatory compliance, and the protection of patient wellbeing throughout the drug lifecycle.

What is the difference between Safety Scientist vs Safety Engineer?

AspectSafety Scientist
Required Credentials
Bachelor's or higher in safety, environmental science, or related field; certifications like ASP or CSP often preferred
Work Environment
Research labs, corporate safety departments, or regulatory agencies
Employer & Industry Usage
Used across manufacturing, healthcare, and chemical industries focusing on safety research and policy development
Comparison Summary

Safety Scientists focus on researching and developing safety protocols, policies, and compliance strategies, often working in labs or policy settings. Safety Engineers, on the other hand, are more involved in designing and implementing safety systems on the ground, such as safety equipment and procedures. Both roles require safety certifications and work within similar industries, but Safety Scientists emphasize research and policy, while Safety Engineers focus on practical safety system implementation.

More about Safety Scientist jobs
What cities are hiring for Safety Scientist jobs? Cities with the most Safety Scientist job openings:
What states have the most Safety Scientist jobs? States with the most job openings for Safety Scientist jobs include:
What job categories do people searching Safety Scientist jobs look for? The top searched job categories for Safety Scientist jobs are:
Safety Scientist jobs near you
Infographic showing various Safety Scientist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $127,745 per year, or $61.4 per hour.

Safety Scientist

Argenx

Remote

Full-time

Medical, Retirement

Posted 19 days ago

Job description

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases.
We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company, our partnerships, our science, and our people, because when we do, we deliver more for patients.
The Safety Scientist is responsible for the ongoing safety surveillance of assigned investigational and/or marketed products. The safety scientist directs a cross functional team comprised of and Medical Safety, Clinical Development, Regulatory Affairs, Biostatistics, and Safety Operations to ensure timely evaluation of safety data, identification of safety signals, and preparation of high-quality safety deliverables. The Safety Scientist contributes to proactive benefit-risk assessment and compliance with global safety reporting requirements. Effective communication and influence with internal and external stakeholders are essential. This role represents GPS Safety Science internally and externally at a global level and functions. The role also applies digital and data fluency - using analytics, visualization, and AI-supported outputs, with sound scientific judgment and awareness of their limitations - to strengthen signal detection and benefit-risk assessment.
ROLES AND RESPONSIBILITIES
  • Conduct continuous review and analysis of aggregate safety data from clinical trials, post-marketing individual case safety reports (ICSRs), literature, registries, and external databases.
  • Identifies data, analytical, or process improvements that increase the likelihood of detecting a signal or decrease the time to signal detection.
  • Leverage data, analytics, visualization, and AI-supported outputs to enhance signal detection, aggregate safety review, and benefit-risk assessment.
  • Critically review and interpret outputs from safety databases, analytics, and AI-enabled tools, applying appropriate scientific judgment and awareness of data limitations, bias, and confounding.
  • Contribute to the design, testing, and continuous improvement of data-driven and automated safety-surveillance workflows, in alignment with quality, validation, and regulatory requirements.
  • In conjunction with safety physician team members, identifies opportunities to increase knowledge of patient treatment, drugs and interactions, and treatment pathways that drive actions and decisions to ensure the safe use of argenx medicines
  • Perform medical coding checks, case series reviews, and standardize MedDRA search strategies.
  • Define data acquisition strategy, methodology, and approach for safety evaluations.
  • Assist in the assessment and management of medical safety data, and in the development and execution of safety signal and benefit-risk management strategies.
  • Contribute and perform analysis and participate actively in safety governance meetings, including Safety Management Team (SMT) and Benefit-Risk Committee (BRC).
  • Lead and participate in the planning, preparation, drafting and review of periodic safety reports, including DSURs, PBRERs/PSURs and PADERs.
  • Facilitate cross-functional input collection from clinical, nonclinical, regulatory, and statistical teams
  • Support the end-to-end signal management process and perform signal detection activities through generation of routine outputs and initial trend evaluations using the appropriate tools and methodologies
  • Lead the identification, analysis, and evaluation of safety signals that arise from multiple internal and external data sources
  • Conduct regular literature reviews to identify new safety information related to company products
  • Assist in the development, maintenance, and execution of Risk Management Plans (RMPs) and Risk Evaluation and Mitigation Strategies (REMS)
  • Support updates to safety labelling sections and Core Data Sheets (CDS), including reviewing proposed safety language and references
  • Represent actively safety cross functionally
  • Support responses to regulatory safety inquiries
  • Partner with Safety Operations on case quality issues, MedDRA coding, and case processing convention
  • Contribute and collaborate with Clinical, Regulatory, and Biostatistics teams to development and review of clinical documents, including CSRs, IBs, protocols, and SAPs
  • Provide contributions at internal audits and regulatory inspections
  • Support the development of and updates to GPS Standard Operating Procedures (SOPs) and other controlled documents (e.g. work instructions, forms, templates)
  • Contribute to the maintenance of the safety databases and tools
  • Participate in cross-functional projects and initiatives
  • Perform other tasks as required to assist in departmental activities

SKILLS AND COMPETENCIES
  • Knowledge of pharmacovigilance as applies to safety signal management, safety data review in clinical and post-marketing settings
  • Ability to assemble, analyze and disseminate knowledge gathered from disparate data sources to drive benefit-risk decision making
  • Knowledge of relevant global pharmacovigilance regulations and guidelines
  • Ability to prepare and/or review high quality safety documents, including periodic aggregate safety reports, signal evaluation report, or risk management plans.
  • Ability to communicate complex issues effectively
  • Ability to influence and collaborate with multidisciplinary teams
  • Ability to prioritize and plan proactively
  • Excellent analytical and problem-solving skills, with sound autonomy and applied judgment
  • Experience with MedDRA, WHO Drug Dictionary
  • Understanding of the principles of databases, querying data sources as well as developing and applying search strategies
  • Strong digital literacy, including the ability to work with safety and real-world datasets and to interpret safety data from dashboards, analytics, and AI- or system-generated outputs, applying sound scientific judgment.
  • Familiarity with analytics, statistical, and visualization tools (e.g. Python, R, SQL, or SAS; Power BI, Tableau, or Spotfire) is an advantage.
  • Familiarity with AI/ML methods relevant to signal detection (e.g. classification, clustering, NLP) and experience automating routine safety-surveillance tasks is an advantage.
  • Fluency in written and spoken English

EDUCATION, EXPERIENCE AND QUALIFICATIONS
  • Master's or doctoral degree in pharmacy, nursing, healthcare or other life sciences or technical fields (MS, PharmD. or PhD)
  • Minimum of 5-7 years of pharmacovigilance/safety risk management experience
  • Experience working with quantitative or real-world safety data and, ideally, with signal-detection or benefit-risk analytics; grounding in statistics or epidemiology is a plus.
  • Experience using GenAI or analytics tools to support drafting of safety documents and data exploration, with a clear understanding of their limitations and the requirement for scientific oversight, is a plus.
  • Familiarity with structured, reproducible, and traceable analysis workflows (e.g. version control or notebooks-as-code) supporting transparent and auditable safety analyses is a plus.

#LI-Remote
For applicants in the United States: The annual base salary hiring range for this position is $164,000.00 - $225,500.00 USD. This range reflects our good faith estimate at the time of posting. Individual compensation is determined using objective, inclusive, and job-related criteria such as relevant experience, skills, demonstrated competencies and internal equity. This means actual pay may differ from the posted range when justified by these factors. Because market conditions evolve, pay ranges are reviewed regularly and may be adjusted to remain aligned with external benchmarks.
This job is eligible to participate in our short-term and long-term incentive programs, subject to the terms and conditions of those plans and applicable policies. It also includes a comprehensive benefits package, including but not limited to retirement savings plans, health benefits and other benefits subject to the terms of the applicable plans and program guidelines.
At argenx, all applicants are welcomed in an inclusive environment. They will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics. argenx is proud to be an equal opportunity employer.
Before you submit your application, CV or any other personal details to us, please review our argenx Privacy Notice for Job Applicants to learn more about how argenx B.V. and its affiliates ("argenx") will handle and protect your personal data. If you have any questions or you wish to exercise your privacy rights, please contact our Global Privacy Office by email at privacy@argenx.com.
If you require reasonable accommodation in completing your application, interviewing, or otherwise participating in the candidate selection process please contact us at hr.us@argenx.com. Only inquiries related to an accommodation request will receive a response.

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