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Safety Scientist Jobs (NOW HIRING)

AstraZeneca

Director, Safety Scientist

Boston, MA · On-site

$175K - $263K/yr

Organize, train and/or support junior safety scientists and fellows across multiple product portfolios and/or indications * Co-lead activities related to new drug applications and other regulatory ...

Grifols

Drug Safety Scientist

Clayton, CA · On-site

They must exhibit a solid knowledge of safety databases with regards to data entry, workflow ... Requirements: * BS in health science field, Pharmacy, CRA, biomedical sciences with 2 years of ...

BeiGene, Inc.

Associate Director, Safety Scientist

The Associate Director Safety Scientist is part of a team that performs high quality and timely scientific and operational safety analysis. This position works closely with the Safety Science group ...

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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.

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What cities are hiring for Safety Scientist jobs? Cities with the most Safety Scientist job openings:
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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.

Director, Drug Safety & Pharmacovigilance - Safety Scientist

Travere Therapeutics

San Diego, CA • On-site

Full-time

Medical, Life, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Department:
106750 Clinical Development
Location:
San Diego, USA- Remote
Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease.
At Travere Therapeutics, we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on meeting the unique needs of rare patients. Our work is rewarding - both professionally and personally - because we are making a difference. We are passionate about what we do.
We are seeking talented individuals who will thrive in our collaborative, diverse, fast-paced environment and share in our mission - to identify, develop and deliver life-changing therapies to people living with rare disease. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community.
At Travere Therapeutics, we are in rare for life. We continue to courageously forge new paths as we move toward a common goal of elevating science and service for rare patients.
Position Summary:
The Director, Drug Safety & Pharmacovigilance (DSPV) Safety Scientist will provide strategic and operational leadership for safety science activities across the company's clinical development and commercial product portfolio. This role is responsible for leading safety signal detection and management, aggregate safety reporting, benefit-risk evaluation, safety surveillance, risk management activities, and regulatory safety responses. The Director, DSPV Safety Scientist will serve as the safety science lead for assigned products and programs, providing expert medical and scientific guidance while ensuring compliance with global pharmacovigilance regulations and company policies.
Responsibilities:
  • Provides strategic leadership for safety surveillance and safety science activities across assigned development and commercial products, including development and implementation of safety monitoring strategies aligned with regulatory requirements and business objectives
  • Leads ongoing benefit-risk evaluations and recommends appropriate risk mitigation strategies for assigned products, programs, or therapeutic areas
  • Represents DSPV on cross-functional governance committees, development teams, and strategic initiatives
  • Performs medical review of ICSRs from clinical trials and postmarket reports (coding, expectedness, causality, seriousness, and narratives) to ensure quality and accuracy of reports
  • Participates in Medical Data Review, including coding review of clinical study data
  • Leads safety signal management activities of assigned products, and oversight of vendor delegated to conduct signal detection, if applicable
  • Leads and/or contributes to the planning, preparation, writing, review and QC of aggregate safety reports (e.g. PADER, PSUR/PBRER, DSUR)
  • Reviews and contributes to safety sections of key study documents such as Investigator Brochures, protocols, statistical analysis plans, informed consent forms, and CSRs
  • Reviews tables, figures, and listings, and safety analyses supporting regulatory submissions
  • Ensures ongoing assessment of risk minimization (such as REMS, RMPs, etc.) effectiveness and regulatory compliance
  • Serves as a subject matter expert during regulatory inspections, audits, and due diligence activities
  • Leads inspection readiness efforts for Safety Science and safety surveillance functions
  • Provides strategic oversight of pharmacovigilance vendor supporting safety science activities
  • Collaborates with Clinical Development, Biostatistics, Regulatory Affairs, Medical Affairs, Medical Writing, and Quality to ensure alignment on safety strategies and deliverables
  • May directly manage other Pharmacovigilance personnel
  • Contributes to the development of risk management plans and product labels (e.g., USPI, EU SmPC)
  • Leads development and continuous improvement of DSPV SOPs and/or Work Instructions
  • Additional duties assigned as needed

Education/Experience Requirements:
  • Bachelor's degree in healthcare professional or related field required. Equitable combination of skills and relevant experience are also considered. RN, PharmD, PA or NP, or equivalent preferred
  • Minimum 10+ years of experience in Drug Safety/Pharmacovigilance for a biotech/ pharmaceutical company in clinical and postmarketing environments
  • 8+ years of progressively increasing leadership responsibility within Safety Science or related field
  • Experience leading safety surveillance, signal detection, aggregate reporting, and benefit-risk assessments
  • Significant experience authoring and/or overseeing DSURs, PSURs/PBRERs, PADERs, and RMPs
  • Strong understanding of global pharmacovigilance regulations including FDA, EMA, ICH, MHRA, and other international requirements
  • Strong knowledge of MedDRA, WHO Drug Dictionary and safety databases (e.g ARGUS, ARISg, etc)

Additional Skills/Experience/Requirements:
  • The ideal candidate will embody Travere's core values: Courage, Community Spirit, Patient Focus and Teamwork
  • Driven, intelligent, passionate about making a difference for patients with rare diseases
  • Strong interpersonal and communication skills; proactive approach. Able to work both independently and in a team environment
  • Detail-oriented, with good organizational, prioritization, and time management proficiencies
  • Proven ability to manage multiple priorities in a fast-paced environment
  • Strong strategic thinking, problem-solving, and decision-making capabilities
  • Nephrology and/or rare disease experience preferred
  • Ability to work effectively across global time zones when necessary
  • Some travel (10-15%) may be required, with the potential for travel occurring over weekends
  • All positions have an essential job function to be able to perform face to face work with colleagues and/or onsite in San Diego.
  • No role is expected to be 100% remote.

Travere is an EEO/AA/Veteran/Disability Employer
Total Rewards Offerings:
Travere provides comprehensive total rewards offerings that demonstrate our commitment as a diverse, equitable, people-centric, and pay-for-performance organization.
Benefits: Our benefits include premium health, financial, work-life and well-being offerings for eligible employees and dependents, wellness and employee support programs, life insurance, disability, retirement plans with employer match and generous paid time off.
Compensation: Our competitive compensation package includes a combination of both cash compensation (base pay and short-term incentive) and long-term incentive compensation (company stock), designed to recognize, retain, and reward employees.
Target Base Pay Range:
$189,000.00 - $246,000.00
*This information is current as of the date of this posting and may be modified in the future. Actual pay offered to a candidate will depend on a variety of factors including the candidate's experience, education, skills, and location.
Travere will accept applications on an ongoing basis until a candidate is selected for the position.
Travere Therapeutics, Inc. is an EEO/AA/Veteran/Disability Employer.
If you require a reasonable accommodation to complete the application or interview process, please contact us by sending an email to accommodations@travere.com. Please note that this email address is to be used exclusively to request an accommodation with the online application, interview or hiring process only. Travere HR will not reply to emails sent to this address for any other reason.

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