1

Clinical Safety Analyst Jobs (NOW HIRING)

$28 - $34/hr

QUALITY & SAFETY ANALYST Substance Use Disorder Treatment CRI-Help is a substance use disorder ... clinicians and clients about how to improve the experience of working in and receiving care from ...

Authoring or reviewing safety sections of clinical documents including but not limited to the clinical study protocol, informed consent form, Investigator's Brochure, statistical analysis plan ...

Preparing aggregate safety reports and conducting signal surveillance clinical development including risk/benefit analysis and safety assessment Risk management and minimization programs Proven skill ...

Showing results 21-40

Clinical Safety Analyst information

See salary details

$18

$39

$62

How much do clinical safety analyst jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for clinical safety analyst in the United States is $39.80, according to ZipRecruiter salary data. Most workers in this role earn between $31.49 and $45.67 per hour, depending on experience, location, and employer.

What is a clinical safety analyst?

Clinical Safety Analysts are healthcare professionals who focus on monitoring, evaluating, and improving patient safety within clinical settings. They analyze data related to adverse events, medication errors, and other safety incidents to identify trends and root causes. Their goal is to develop strategies and protocols that reduce risks and enhance the quality of patient care. Clinical Safety Analysts often collaborate with medical staff, quality improvement teams, and regulatory bodies to ensure compliance with safety standards and promote a culture of safety in healthcare organizations.

What are the main challenges clinical safety analysts face when working with multidisciplinary teams?

Clinical Safety Analysts often collaborate with clinicians, data scientists, regulatory affairs, and quality assurance teams. One common challenge is ensuring clear communication across disciplines, as each group may use different terminology or focus on different priorities. Balancing regulatory compliance with real-world clinical needs can also require strong negotiation and problem-solving skills. Building strong relationships and maintaining a proactive approach to information sharing are essential for success in this collaborative environment.

What are the key skills and qualifications needed to thrive as a clinical safety analyst, and why are they important?

To thrive as a Clinical Safety Analyst, you need a strong background in clinical research, pharmacovigilance principles, and data analysis, often supported by a degree in life sciences or a related field. Familiarity with safety databases (such as Argus or ARISg), regulatory reporting systems, and relevant certifications like Certified Clinical Research Professional are commonly required. Attention to detail, analytical thinking, and effective communication are vital soft skills for identifying and reporting safety concerns. These skills ensure accurate safety monitoring, regulatory compliance, and the protection of patient well-being in clinical settings.
More about Clinical Safety Analyst jobs

What cities are hiring for Clinical Safety Analyst jobs?

Cities with the most Clinical Safety Analyst job openings:

What are popular job titles related to Clinical Safety Analyst jobs?

For Clinical Safety Analyst jobs, the most frequently searched job titles are:

Infographic showing various Clinical Safety Analyst job openings in the United States as of September 2026, with employment types broken down into 2% As Needed, 76% Full Time, 20% Part Time, 1% Contract, and 1% Nights. Highlights an 98% Physical, and 2% Remote job distribution, with an average salary of $82,791 per year, or $39.8 per hour.

Distinguished Scientist. Nonclinical Safety Leader

Cambridge, MA โ€ข On-site

Full-time

Retirement, PTO

Posted 9 days ago


Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Discovery & Pre-Clinical/Clinical Development

Job Sub Function:

Nonclinical Safety

Job Category:

Scientific/Technology

All Job Posting Locations:

Cambridge, Massachusetts, United States of America, Spring House, Pennsylvania, United States of America

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

Johnson & Johnson Innovative Medicine R&D is recruiting for a Distinguished Scientist, Nonclinical Safety Leader within Preclinical Sciences and Translational Safety (PSTS). This position is a hybrid role and can be located in Spring House, PA or Cambridge, MA.

As a Distinguished Scientist, Nonclinical Safety (NCS) Leader, you will collaborate with innovative and diverse scientists to support projects in our large and varied portfolio that spans multiple therapeutic areas and includes innovative modalities. In this vital role you will provide toxicology leadership for all aspects of discovery and development projects, with flexibility to specialize or work across stages of development, therapy areas, and modalities. You will also collaborate with discovery scientists to identify and nominate candidate molecules, and with development teams to bring these molecules to humans and ultimately through global registration.

Principal Responsibilities:

  • Lead PSTS project teams of nonclinical safety and Pharmacokinetic (PK) scientists, ensuring efficient information transfer within the team and interfacing with senior management.

  • Serve as NCS representative for global project teams, providing strategic leadership, toxicology expertise, and matrix leadership to ensure high-quality, data-driven decisions that enable efficient progression of portfolio assets from target assessment through commercialization.

  • Create target risk assessments and develop plans to screen for and mitigate potential risks; analyze toxicology and safety pharmacology studies, contextualizing results for human safety and preparing nonclinical safety assessments.

  • Contribute to issue-resolution teams by generating hypotheses and investigative strategies.

  • Accountable for global regulatory nonclinical documents and health authority responses to support clinical trials and compound registrations.

  • Participate in medical safety teams, signal detection analyses, and risk mitigation strategies.

  • Engage in nonclinical safety risk assessments for due diligence of potential Licensing and Acquisition (L&A) opportunities.

  • Collaborate proactively with Chemistry, Manufacturing and Controls (CMC) functions to assure drug substance quality.

  • Actively participate in external academic or industry societies and consortia to enhance toxicology strategies and capabilities.

  • Maintain scientific depth and knowledge in competitive intelligence and regulatory landscapes for assigned projects.

  • Communicate effectively with stakeholders, including regulatory authorities, leveraging drug development experience.

  • Provide leadership and mentorship within the PSTS organization.

  • Lead strategic initiatives as required.

  • This role may have future-facing people leadership responsibilities, as needed.

Qualifications:

  • A minimum of a Master's degree in Toxicology, Pharmacology or a related discipline is required. Doctoral level degree (PhD, DVM, MD or equivalent) in Toxicology, Pharmacology or related discipline is preferred.

  • A minimum of 15 years of relevant pharmaceutical/biotech industry experience with a Master's degree or a minimum of 10 years of relevant pharmaceutical/biotech industry experience with a doctoral level degree (PhD, DVM, MD or equivalent) is required.

  • Proven experience in representing toxicology/nonclinical safety on multi-disciplinary project teams is required.

  • Strong understanding of the drug discovery and development process is required.

  • Experience in conducting due diligence activities is preferred.

  • Previous experience as a Study Director/Study Monitor under Good Laboratory Practice (GLP) regulations is preferred.

  • Familiarity with diverse and emerging/specialized therapeutic modalities is preferred.

  • Board certification (e.g. Diplomate of the American Board of Toxicology (DABT)) is preferred.

  • Must have excellent oral and written communication skills.

  • The ability to collaborate with all levels in a cross-functional team environment is required.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.

#LI-Hybrid

Required Skills:

Preferred Skills:

Consulting, Design Mindset, Drug Discovery Development, EHS Compliance, Emergency Planning, Performance Measurement, Process Hazard Analysis (PHA), Process Optimization, Program Management, Regulatory Affairs Management, Research and Development, Risk Management, Safety Audits, Safety Investigations, Safety-Oriented, Scientific Research, Stakeholder Engagement, Strategic Thinking, Technical Writing

The anticipated base pay range for this position is :

$164,000.00 - $282,900.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company's long-term incentive program.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation -120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year
Holiday pay, including Floating Holidays -13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave - 80 hours in a 52-week rolling period10 days
Volunteer Leave - 32 hours per calendar year
Military Spouse Time-Off - 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits