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Clinical Safety Scientist Jobs (NOW HIRING)

Viridian Therapeutics, Inc.

Safety Scientist

Waltham, MA · On-site +1

$127K - $155K/yr

This role involves monitoring, analyzing, and assessing adverse events and other safety data from clinical trials and other sources, to identify and validate safety signals. The Safety Scientist ...

Argenx

Safety Scientist

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 ...

Merck & Co.

Principal Scientist, Nonclinical Drug Safety Program Discovery - Equivalent in level to Scientific Director We are seeking a Discovery Program Leader (DPL) to represent Nonclinical Drug Safety (NDS ...

Merck & Co.

Principal Scientist, Nonclinical Drug Safety Program Discovery - Equivalent in level to Scientific Director We are seeking a Discovery Program Leader (DPL) to represent Nonclinical Drug Safety (NDS ...

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Clinical Safety Scientist information

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How much do clinical safety scientist jobs pay per hour?

As of Aug 1, 2026, the average hourly pay for clinical safety scientist in the United States is $54.75, according to ZipRecruiter salary data. Most workers in this role earn between $40.14 and $68.27 per hour, depending on experience, location, and employer.

How does a Clinical Safety Scientist typically collaborate with cross-functional teams during a clinical trial?

Clinical Safety Scientists work closely with medical monitors, data management teams, regulatory affairs, and clinical operations to ensure participant safety throughout a clinical trial. They are often responsible for reviewing and analyzing safety data, preparing safety reports, and contributing to risk management strategies. Regular communication and collaboration are essential, as Clinical Safety Scientists must provide timely updates on safety findings and coordinate responses to emerging safety issues. This teamwork helps ensure regulatory compliance and the overall success of the trial.

What are Clinical Safety Scientists?

Clinical Safety Scientists are professionals in the pharmaceutical and biotechnology industries who are responsible for monitoring and evaluating the safety of drugs and medical products during clinical trials and after they reach the market. They analyze safety data, identify potential risks, and ensure that any adverse effects are properly reported to regulatory authorities. Their work is crucial in ensuring patient safety and compliance with global health regulations.

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

A Clinical Safety Scientist should have a solid background in life sciences, pharmacovigilance, and drug safety, often supported by a relevant degree and experience in clinical research. Familiarity with safety databases (like Argus or ArisG), MedDRA coding, and regulatory reporting systems is typically required, along with certifications such as those from DIA or RQA being advantageous. Excellent analytical skills, attention to detail, and strong communication abilities are essential soft skills for interpreting safety data and collaborating with cross-functional teams. These competencies ensure accurate safety assessments, regulatory compliance, and the protection of patient well-being throughout clinical development.

What is the difference between Clinical Safety Scientist vs Pharmacovigilance Specialist?

AspectClinical Safety ScientistPharmacovigilance Specialist
Required CredentialsLife sciences degree, safety certificationsLife sciences degree, safety certifications
Work EnvironmentPharmaceutical companies, clinical trial settingsPharmaceutical companies, safety monitoring teams
Employer & Industry UsageUsed in clinical development and safety assessmentUsed in drug safety monitoring and adverse event reporting

The Clinical Safety Scientist and Pharmacovigilance Specialist roles share similar credentials and work environments, often overlapping in pharmaceutical companies. The main difference lies in focus: Clinical Safety Scientists primarily assess safety data during clinical trials, while Pharmacovigilance Specialists monitor and report adverse events post-approval. Both roles are essential for ensuring drug safety throughout the product lifecycle.

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Clinical Safety Scientist jobs near you
Infographic showing various Clinical Safety Scientist job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $113,877 per year, or $54.7 per hour.

Senior Director, Clinical Safety Scientist

Daiichi Sankyo, Inc.

Basking Ridge, NJ • On-site

$242K - $404K/yr

Full-time

Re-posted 4 days ago

Job description

Senior Director, Clinical Safety Scientist
Job Requisition ID: 1430
Posting Start Date: 4/28/26
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary
The Senior Director, Clinical Safety Science is a key leadership role responsible for shaping and advancing global safety strategy across the product lifecycle-from early development through post-marketing. This position oversees a team of Safety Scientists who partner with Safety Physicians and cross-functional stakeholders to ensure proactive safety surveillance, benefit-risk assessment, and risk mitigation planning for a group of assets. The Senior Director plays a pivotal role in influencing safety governance, driving innovation in safety science, and ensuring regulatory and compliance excellence. In addition to operational oversight, this role contributes to the development of global safety processes, talent capability building, and strategic alignment across the broader Clinical Safety and Pharmacovigilance (CSPV) function and the enterprise.
Job Description
Responsibilities
  • Strategic Safety Leadership: Provide scientific and strategic leadership for safety surveillance and risk management for a group of assets. Lead scientist team to collaborate with safety physicians, regulatory affairs, clinical development, other functions and external partners to deliver high-quality safety assessments, regulatory submissions, aggregate reports, and responses to health authority queries.
  • Team and Talent Development: Lead, mentor, and develop a high-performing team of safety scientists supporting a group of assets. Champion a culture of scientific rigor, continuous learning, and collaboration. Ensure strategic alignment of talent to pipeline priorities, provide performance feedback, and guide professional growth to build future leadership.
  • Innovation and Process Excellence: Maintain strong knowledge of the evolving safety science and regulatory landscape. Drive initiatives to enhance scientific methods, tools, and systems supporting safety surveillance and signal detection. Lead cross-functional and global projects to evolve safety science capabilities. Contribute to strategic planning and operating model design for CSPV.
  • Compliance and Quality Oversight: Ensure all safety deliverables by the scientist team meet internal quality standards and are compliant with GCP/GVP and relevant global regulations. Support audits and inspections, contribute to CAPA development, and foster a culture of quality and accountability.
  • Resource Planning: Partner with CSPV portfolio management and product leads to forecast resource needs for a group of assets and align capacity with business priorities. Leverage metrics to inform decision-making and improve operational efficiency.

Qualifications
Education Qualifications
  • PharmD or PhD degree in relevant discipline required

Experience Qualifications
  • At least 10 years of experience in clinical development, medical affairs or clinical safety/post marketing safety in the pharmaceutical industry required
  • At least 5 years of experience in clinical safety/post marketing safety in the pharmaceutical industry preferred
  • At least 5 years of people management experience required
  • Experience in leading safety scientist teams in clinical studies, regulatory submissions, aggregate reports and post-marketing surveillance and risk management
  • Excellent communication, project management, writing and analytic skills
  • Demonstrated strong organizational leadership skills
  • Extensive knowledge of the latest technical and regulatory development

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range:
USD$242,700.00 - USD$404,500.00
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