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Clinical Events Adjudication Jobs (NOW HIRING)

NAMSA

Safety Associate

$75K/yr

Gathers member documents, develops member contracts, tracks events for adjudication, prepares ... with clinical research experience. Experience and use in EDC database and / or Safety database ...

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Clinical Events Adjudication information

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How much do clinical events adjudication jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for clinical events adjudication in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What is the difference between Clinical Events Adjudication vs Clinical Data Coordinator?

AspectClinical Events AdjudicationClinical Data Coordinator
CredentialsTypically requires clinical or research experience, sometimes certifications in clinical researchOften requires a degree in health sciences or related field, with data management certifications
Work EnvironmentResearch settings, clinical trials, healthcare organizationsHospitals, clinics, research institutions, data management departments
Job FocusReviewing and confirming clinical events in trialsCollecting, managing, and ensuring accuracy of clinical data

Clinical Events Adjudication specialists focus on reviewing and confirming clinical events in research studies, ensuring data accuracy for trial outcomes. Clinical Data Coordinators handle data collection and management, supporting the integrity of clinical trial data. While both roles work within clinical research, their responsibilities and focus areas differ significantly.

What are popular job titles related to Clinical Events Adjudication jobs?

For Clinical Events Adjudication jobs, the most frequently searched job titles are:

Infographic showing various Clinical Events Adjudication job openings in the United States as of September 2026, with employment types broken down into 3% As Needed, 74% Full Time, 16% Part Time, and 7% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Safety Monitor

Maple Grove, MN • On-site

Arnex Solutions LLC
IT Services • 11 - 50 employees
Learn more about Arnex Solutions LLCexternal

Other

This job post has expired today. Applications are no longer accepted.

Job description

Monitor, Maplegrove, MN Role Summary    

The Safety Monitor ensures that clinical studies are planned and conducted in compliance with applicable regulations, Good Clinical Practices, and standard operating procedures. The primary focus of this role is the processing and review of adverse events, ensuring the consistency, completeness, and regulatory compliance of safety data for assigned studies.

Key Responsibilities    

•       Processes all adverse events per the Clinical Investigational Plan (CIP) and applicable Work Instructions, ensuring regulatory and CIP compliance in safety data processing.

•       Reviews adverse events in a timely manner for consistency and completeness of safety data.

•       Ensures source documents related to submitted adverse events are reviewed per the Safety Plan; confirms consistency between source documents and safety data points; creates and processes safety data queries for inconsistent or ambiguous data.

•       Collaborates with study-specific Safety CRAs to ensure comprehensive information is available for Clinical Event Committee (CEC) review and adjudication.

•       Assists in drafting the Safety Plan for assigned studies.

•       Assists in reconciliation between submitted adverse events and product complaints, and between adverse events and other related forms per the Safety Plan.

•       Acts as the safety representative for the Clinical Study team; serves as a liaison to project management and site personnel on safety-related issues.

•       Reviews and provides comments on safety-related study documents.

•       Supports follow-up and resolution of safety data findings from monitoring visits and audits.

•       Develops and maintains knowledge of regulations and guidelines for classifying and reporting adverse events.

•       May contribute to the development of safety documents and guidance for the safety team.

Required Qualifications    

•       Bachelor’s degree in medicine, pre-medicine, nursing, life science, bioengineering, or a related field.

•       Minimum 2 years of clinical research experience.

•       Understanding of medical terminology.

•       Ability to interpret basic safety data and communicate findings effectively across all levels.

•       Strong written and verbal communication, interpersonal, presentation, and organizational skills.

•       Ability to work independently while seeking guidance when appropriate.

•       Proficiency in Microsoft Office Suite and relevant clinical applications.

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