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Clinical Events Adjudication Jobs (NOW HIRING)

Shifamed

Sr. Clinical Safety Specialist

Los Gatos, CA · On-site

$120K - $150K/yr

Direct experience working with a Clinical Events Committee (CEC) or adjudication committee, including case preparation and presentation. * Working knowledge of FDA device safety reporting ...

Shifamed

Sr. Clinical Safety Specialist

Los Gatos, CA · On-site

$125 - $150/hr

Direct experience working with a Clinical Events Committee (CEC) or adjudication committee, including case preparation and presentation. * Working knowledge of FDA device safety reporting ...

Socket.dev

Sr. Clinical Safety Specialist

Los Gatos, CA · On-site

$125 - $150/hr

Direct experience working with a Clinical Events Committee (CEC) or adjudication committee, including case preparation and presentation. * Working knowledge of FDA device safety reporting ...

BD Mexico

Clinical Safety Specialist

Tempe, AZ · On-site

$100 - $125/hr

... Event Trending Meetings, CEC Adjudication/Meetings, DMC Meetings, safety-related study team ... Mentor Clinical Safety personnel and conduct evaluations for other Clinical Safety personnel, as ...

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All JobsClinical Events Adjudication Jobs

Clinical Events Adjudication information

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How much do clinical events adjudication jobs pay per hour?

As of Sep 8, 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.

Specialist, Clinical Safety (US Remote)

MicroVention

Aliso Viejo, CA • On-site, Remote

$105K - $131K/yr

Full-time

Re-posted yesterday

Key responsibilities

  • Provide clinical safety support to assigned clinical studies, including safety documentation, adverse event review, safety investigations, and management of safety committees.

  • Draft, review, and contribute to clinical safety documentation such as study protocols, reports, manuals, CRFs, and related materials.

  • Review and triage adverse events, prepare documentation for independent review, and manage the proceedings of physician safety committees and related activities.

Job description


Support clinical safety aspects of MicroVention clinical studies. Job duties:
  • Provide all required clinical safety support to assigned clinical studies, including study safety documentation development, adverse events (AE) review, safety investigations, and startup/management of independent safety committees/ adjudicators.
  • Draft, review, and provide input to the clinical safety components of clinical study protocols, study reports, safety manuals, safety CRFs, study supporting materials, and other related documentation.
  • Review and triage study adverse events and prepare for independent physician or committee review by preparing/tabulating these events, gathering relevant source documentation, and preparing narratives.
  • Schedule and manage the proceedings of physician safety committees including Clinical Events Committees (CECs) and Data Safety Monitoring Boards (DSMBs), as well as the activities of independent Clinical Events Adjudicators (CEAs).
  • Support the selection of physician partners, including CEA/CEC/DSMB delegates and other committee members, and provide all required training.
  • Generate and present reports to physician safety committees as well as reports of committee findings and results.
  • Partner with clinical research project managers and Medical Affairs and Safety Manager to ensure safety startup activities and pace of events adjudication aligns with study timeline and milestones and to provide regular progress updates.
  • Support clinical science and regulatory affairs functions by utilizing medical expertise to provide input to study design, clinical evaluation reports, clinical study reports, literature review, risk management, regulatory submissions, questions from regulatory authorities, scientific analyses, and other scientific documentation.
  • Support clinical project management function by utilizing medical expertise to provide input to protocol development, risk/benefit analyses, adverse events review, adverse events reporting, investigator questions, investigator meetings, clinical study reports, and other related documentation/activities.
  • Minimal domestic travel required (1 - 3 trips per year).
  • Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
  • Perform additional duties as assigned.

Qualifications
  1. RN/BSN or equivalent.
  2. Minimum one (1) to three (3) years of experience providing clinical safety support to regulated clinical device studies or relevant clinical research experience, academic experience, or experience in a hospital setting.
  3. Ability to produce high-quality scientific communications and narratives.
  4. Strong written and verbal communication skills.
  5. Strong interpersonal skills to build effective relationships with geographically diverse physicians and internal business partners.
  6. Strong detail-orientation and organizational/time management skills.
  7. Proficiency in standard computer programs including MS Office (Word, Excel, PowerPoint, Outlook, Teams, etc.).
  8. Ability to maintain strict confidentiality.
Desired Qualifications
  1. MD or foreign equivalent.
  2. Clinical, academic, CRO, or industry experience in a relevant field (neurology, neuroradiology, or neurosurgery).
  3. Knowledge of GCP, FDA, and ICH regulations and guidelines.
  4. Knowledge and experience in the detection, understanding, review, investigation, and assessment of adverse events.
  5. Class III medical device safety experience.
Physical
  • Extended periods of computer use.
  • Extended periods of sitting or standing.
  • Light lifting, up to 25 lbs.
  • May be required within the position to be in an environment that can include radiation exposure (such as in Cathlabs).
  • Minimal domestic travel required (1 - 3 trips per year).
EEO
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, veteran status, marital status or any other characteristics protected by law.
Fair Chance Ordinance
If you are applying to perform work for Terumo Neuro in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Terumo Neuro reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Terumo Neuro will consider for employment qualified job applicants with arrest or conviction records in accordance with the California Fair Chance Act, Los Angeles County Fair Chance Ordinance for Employers, Fair Chance Initiative for Hiring Ordinance, and San Francisco Fair Chance Ordinance.
Salary Range
$105,067 - $131,333 (Financial compensation packages may be higher/lower than listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand)

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