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How much do medical safety reviewer jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for medical safety reviewer in the United States is $25.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $28.61 per hour, depending on experience, location, and employer.

What are the typical challenges faced by medical safety reviewers when evaluating adverse event reports?

Medical Safety Reviewers often encounter challenges such as managing large volumes of complex safety data, interpreting ambiguous or incomplete case information, and staying current with evolving regulatory requirements. They must carefully assess the clinical relevance and potential impact of each adverse event while collaborating closely with cross-functional teams such as clinical operations, regulatory affairs, and pharmacovigilance. Effective communication, attention to detail, and strong critical thinking skills are essential to ensure patient safety and regulatory compliance.

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

To thrive as a Medical Safety Reviewer, you need a strong background in clinical medicine, pharmacovigilance, and drug safety, often supported by a medical degree (MD, PharmD, or equivalent) and relevant experience. Familiarity with safety databases (such as Argus or ArisG), regulatory guidelines (ICH, FDA, EMA), and safety signal detection tools is typically required. Attention to detail, analytical thinking, and effective communication are important soft skills for interpreting data and collaborating with cross-functional teams. These skills ensure accurate safety evaluations, regulatory compliance, and the protection of patient well-being in pharmaceutical development.

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

AspectMedical Safety ReviewerPharmacovigilance Associate
Required CredentialsMedical degree or related certification, pharmacovigilance trainingBachelor's degree, training in pharmacovigilance or drug safety
Work EnvironmentPharmaceutical companies, CROs, regulatory agenciesPharmaceutical companies, CROs, clinical research settings
Industry UsageFocuses on safety data review and assessmentSupports safety data collection and reporting
Common Search/ComparisonMedical Safety Reviewer vs Pharmacovigilance Associate

The Medical Safety Reviewer and Pharmacovigilance Associate roles both operate within the drug safety field but differ mainly in responsibilities and qualifications. Medical Safety Reviewers typically have medical degrees and focus on detailed safety data assessment, while Pharmacovigilance Associates often have a bachelor's degree and support data collection and reporting processes. Both roles are essential in ensuring drug safety and regulatory compliance.

What is a medical safety reviewer?

Medical Safety Reviewers are healthcare professionals who assess and monitor the safety of pharmaceutical products, medical devices, or clinical trial data. They review adverse event reports, analyze safety data, and ensure compliance with regulatory requirements to protect patient well-being. Their work is crucial in identifying potential risks and recommending actions to minimize harm, such as updating product information or implementing risk mitigation strategies. Medical Safety Reviewers typically collaborate with regulatory authorities, clinical teams, and pharmacovigilance departments.
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Medical Safety Reviewer jobs near you
Infographic showing various Medical Safety Reviewer job openings in the United States as of July 2026, with employment types broken down into 66% Full Time, 17% Part Time, and 17% Contract. Highlights an 83% In-person, and 17% Remote job distribution, with an average salary of $53,254 per year, or $25.6 per hour.

Senior Manager, Medical Safety

Gateway Recruiting

Minneapolis, MN • On-site

Full-time

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

Job description

Position Summary:

This role is responsible for the implementation of practices, policies, and processes for the Interventional Oncology and Embolization Medical Safety team to ensure medical expertise, objective oversight and safety vigilance throughout the total product lifecycle. The Senior Manager, Medical Safety provides oversight, manages and facilitates the completion of accurate, timely, and consistent medical assessments of adverse events and potential adverse events. The Senior Manager, Medical Safety provides leadership to Medical Safety Professionals (non-MDs) to provide high level medical/ therapeutic guidance to internal and external customers. This role may also include individual contributor responsibilities related to Medical Safety oversight of sustaining Interventional Oncology and Embolization therapies and new product development.

Responsibilities:

  • Ensure the processes and training curriculum are current to support medical safety oversight and input into Clinical (company sponsored clinical trials) and Quality (product complaint handling)
  • Support risk documentation creation and updates, post-market surveillance reports, clinical trial safety documents
  • Support the Quality organization and assist in the creation, implementation, and harmonization of standard policies and procedures
  • Recognize and direct organizational development needs and opportunities for continuous improvement within Medical Safety
  • In partnership with the Medical Director, this role aligns medical safety strategy, escalates emerging safety signals, and ensures consistent medical decision-making across the product lifecycle.
  • Drive comprehensive, integrated analysis of a potential safety issue throughout the product lifecycle
  • Ensure early medical review of clinical trial Adverse Events to identify unanticipated adverse device effects
  • Represent Medical Safety in cross functional working groups on matters affecting patient safety in functional areas such as clinical studies, post market surveillance and risk management
  • Serve as Acquisition Lead for Medical Safety, participating in integration work groups and identifying potential resourcing needs
  • Manage resourcing needs of the team by maintaining key metrics and allocating resources to achieve feasible workloads and meet deadlines. May also include completing financial reports
  • Leading through Change: With organizational change comes stress and uncertainty- provide support and leadership to analyst team through change and ongoing reorganization
  • Work with leadership to identify work process changes/improvements, convey information to analyst team as available/appropriate

Required Qualifications:

  • Holds current and active RN, NP, CRNP, DNP, or PA license
  • Minimum of 8 years of experience providing direct patient care, preferably in oncology or interventional radiology.
  • Minimum of 5 years of experience within the medical device, pharmaceutical, or related health care industry.
  • Minimum of 2 years of experience leading, managing, or supervising clinical or professional staff.
  • Demonstrated leadership skills, including communication, collaboration, strategic planning, innovation, and critical thinking

Preferred Qualifications:

  • Proven experience as an oncology, interventional radiology, critical care nurse, or advanced practice provider.
  • Demonstrated proficiency in staff leadership, coaching, and professional development.
  • Experience supporting operational safety activities for clinical studies and medical devices.
  • Knowledge of ISO standards, IMDRF coding, and MedDRA coding practices.