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Medical Safety Reviewer Jobs (NOW HIRING)

SPECTRAFORCE

Medical Safety Physician

Lincolnton, NC · Remote

Medical Safety Physician 6-month assignment 100% Remote What are the three most important ... Responsibilities Essential Functions Perform medical review and clarification of trial-related ...

Spectra force

Medical Safety Physician

Lincolnton, NC · On-site +1

Participates in all aspects of the Medical Safety activities as per scope of work, such as performing medical review and clarification of trial-related Adverse Events including review of analysis of ...

Argenx

Medical Safety Lead

The Medical Safety Lead provides strategic medical safety leadership, serving as the single point ... Knowledge of pharmacovigilance as applies to safety signal management, safety data review in ...

Jj

Medical Safety Officer, Immunology

Horsham, PA

Reviewing and approving (i.e., signatory) medical assessment reports (e.g., ad hoc safety reports). * Work across the GMS TAs to align and improve common processes including providing strong ...

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How much do medical safety reviewer jobs pay per hour?

As of Jul 17, 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 are Medical Safety Reviewers?

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 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $53,254 per year, or $25.6 per hour.
Medical Safety Physician

Medical Safety Physician

SPECTRAFORCE

Lincolnton, NC • Remote

Contractor

Re-posted 3 days ago

Job description

Job Description

Medical Safety Physician
6-month assignment
100% Remote
What are the three most important qualifications: Argus experience, self starter, experience in pharmacovigilance and infection disease vaccines

Licenses/Certifications: A Valid medical license (active or inactive), or equivalent, from the country or region in which he/she resides and works
Description
Delivers medical, clinical and scientific advisory expertise in clinical research studies and post marketing programs (RWI). Signal detection and aggregated reporting.
Provides medical, scientific and therapeutic expertise on pharmacovigilance services.
Participates in all aspects of the Medical Safety activities as per scope of work, such as performing medical review and clarification of trial-related Adverse Events including review of analysis of similar events, medical evaluation of post-marketing adverse drug reactions, review medical inputs for into signal management and benefit-risk evaluation of drugs in clinical trial and post marketing set up, safety aggregate report review, safety review of study protocol, investigators brochure and other reference safety information, clinical study report narrative review, providing medical assessment comments etc. and serving as an internal consultant for any medical support for pharmacovigilance operations.
Responsibilities
Essential Functions
Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary
Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements
Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported
Provide aggregate reviews of safety information, including clinical data, to maintain oversight of a product's safety profile
Provide coding review of AEs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data
Represent safety and clinical data review findings during client meetings
Provide medical review and edits to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports
Provide medical review and edits of Development Risk Management Plans, EU Risk Management Plans or US Risk
Evaluation and Mitigation Strategies
Provide medical oversight for label development, review and change
Provide medical support and attendance at Data Safety Monitoring Board Meetings
Attends and contributes medical safety evaluation on Safety Monitoring Committees
Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document
Provide medical review and edits to Drug Safety Reports or other benefit-risk assessments
Review and sign off on both the Project Safety Plan and the Medical Monitoring Plan per medical safety scope agreed in contract
Perform Medical Safety review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs) for appropriate safety content and data capture.
Act as Global Safety Physician or Assistant or Back-up on projects as assigned
Attend project meetings, medical safety team meetings, and client meetings as requested
Ensure coverage for all medical safety deliverables within regulatory or contracted timelines
Provide medical escalation support for medical information projects
Provide medical escalation support for EU Qualified Persons for Pharmacovigilance projects
24 hour medical support as required on assigned projects
Maintain awareness of medical-safety-regulatory industry developments
Experience
Typically requires 5 - 7 years of prior relevant experience.
Knowledge
Requires deep knowledge of one or more related job areas typically obtained through advanced education combined with experience.
Typically viewed as having a specialty within discipline.
Education: A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
Skills & Abilities:
Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including
knowledge of regulations and guidelines pertaining to safety and good clinical practice
Knowledge of clinical trials and pharmaceutical research process
Ability to establish and meet priorities, deadlines, and objectives.
Skills in providing consultation and advice on multiple assignments required, as well as initiative and flexibility
Ability to establish and maintain effective working relationships with coworkers, managers and clients
Physical Demands:
Sit at a desk or table with some walking, standing, bending, stooping, or carrying of light objects.
Perform continuous operation of a personal computer for four hours or more.
Use hands and fingers to handle and manipulate objects and/or operate equipment.

Additional Information

All your information will be kept confidential according to EEO guidelines.

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