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Clinical Safety Reviewer Jobs (NOW HIRING)

AstraZeneca

Director, Safety Scientist

Boston, MA · On-site

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 ...

Olema Oncology

Director, Safety Sciences

Boston, MA · On-site

Author and review integrated safety documents, including the Integrated Summary of Safety (ISS), Summary of Clinical Safety (SCS), benefit-risk assessments, and clinical overviews. * Collaborate and ...

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How much do clinical safety reviewer jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical safety reviewer in the United States is $35.92, according to ZipRecruiter salary data. Most workers in this role earn between $31.25 and $40.38 per hour, depending on experience, location, and employer.

What is a clinical safety reviewer?

Clinical Safety Reviewers are professionals responsible for evaluating and monitoring the safety of pharmaceutical products and medical devices during clinical trials. They review clinical data to identify potential safety concerns, assess adverse event reports, and ensure that all regulatory requirements regarding patient safety are met. Clinical Safety Reviewers collaborate with medical teams, regulatory agencies, and other stakeholders to ensure the safety and well-being of trial participants. Their work is crucial in minimizing risks and ensuring that treatments are safe before they reach the market.

How does a clinical safety reviewer typically collaborate with other teams during the drug development process?

Clinical Safety Reviewers work closely with cross-functional teams such as clinical operations, data management, medical monitors, and regulatory affairs. They regularly communicate findings from safety data analyses, contribute to safety review meetings, and provide input for safety sections in regulatory submissions. This collaborative approach ensures that safety signals are identified early and managed appropriately, supporting both patient wellbeing and project timelines. Strong teamwork and clear communication are essential for success in this role.

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

To thrive as a Clinical Safety Reviewer, you need a strong background in life sciences or pharmacy, experience in pharmacovigilance, and knowledge of regulatory requirements such as ICH guidelines. Familiarity with safety databases (like Argus or ArisGlobal), MedDRA coding, and case processing systems is typically required. Attention to detail, critical thinking, and effective communication are standout soft skills in this role. These capabilities ensure accurate safety assessment, regulatory compliance, and the protection of patient well-being in clinical trials.

What is the difference between Clinical Safety Reviewer vs Pharmacovigilance Associate?

AspectClinical Safety ReviewerPharmacovigilance Associate
Required CredentialsBachelor's degree, life sciences background, possibly certification in drug safetyBachelor's degree, life sciences background, often entry-level
Work EnvironmentPharmaceutical companies, CROs, clinical trial settingsPharmaceutical companies, CROs, regulatory agencies
Employer & Industry UsageFocuses on safety data review during clinical trials and post-marketingSupports safety data processing, case entry, and reporting
Common Search & Comparison IntentUnderstanding safety review roles in clinical trialsEntry-level safety data support roles

The Clinical Safety Reviewer primarily evaluates safety data during clinical trials and post-marketing, requiring specialized safety knowledge. In contrast, the Pharmacovigilance Associate handles data entry, case processing, and supports safety reporting. Both roles are essential in drug safety but differ in responsibilities and experience levels.

More about Clinical Safety Reviewer jobs

What job categories do people searching Clinical Safety Reviewer jobs look for?

The top searched job categories for Clinical Safety Reviewer jobs are:

Clinical Safety Reviewer jobs near you
Infographic showing various Clinical Safety Reviewer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 17% Part Time, 1% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $74,707 per year, or $35.9 per hour.

Remote Senior Medical Reviewer-Rheumatology

Medical Devices and Supplies

Great Lakes, IL • On-site

$50 - $80/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

New

Job description

Medical Reviewer / Safety Reviewer III

The Medical Reviewer / Safety Reviewer III will provide medical and scientific oversight to support Medical Affairs activities within the immunology and rheumatology space. This role will review and approve promotional and medical materials while ensuring alignment with medical strategy, regulatory requirements, and industry standards. The position will collaborate closely with cross functional teams and provide medical expertise to support product and commercial initiatives.

Key Responsibilities:

  • Provide medical oversight for the scientific review and approval of promotional and medical materials in accordance with corporate standards and applicable regulations.
  • Collaborate with medical leads to ensure promotional and non promotional materials align with established medical strategy.
  • Provide medical and scientific expertise to support promotional claims, target audiences, product expertise, and related initiatives.
  • Partner with cross functional teams to incorporate current medical and scientific information into departmental resources.
  • Support Medical Affairs teams with medical review activities related to immunology and rheumatology.
  • Apply strong clinical and scientific judgment when evaluating medical content and supporting materials.

Required Qualifications:

  • Demonstrated experience working as a Medical Reviewer.
  • Strong experience in Immunology, with particular preference for Rheumatology experience.
  • Experience with medical review processes and promotional material review.
  • Experience using Veeva PromoMats or a comparable medical content review platform.
  • Advanced degree such as PharmD, Doctor of Medicine, or a master's degree in Biology or Chemistry.
  • Strong understanding of medical, scientific, regulatory, and industry requirements applicable to promotional and medical materials.

Preferred Qualifications:

  • Experience supporting Medical Affairs within the pharmaceutical or biotechnology industry.
  • Previous experience supporting rheumatology focused medical or commercial teams.
  • Strong cross functional collaboration and communication skills.

Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, and paid holidays annually – as applicable.

Pay Range: $50/hr to $80/hr

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