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Clinical Trial Adjudication Jobs (NOW HIRING)

ICON

Adjudication Project Manager

Blue Bell, PA · On-site

The Adjudication Project Manager is primarily responsible for managing all endpoint adjudication processes for a clinical trial. Location: United States (Remote) What you will be doing: * Manages ...

Icon plc

Adjudication Project Manager

Blue Bell, PA · Remote

The Adjudication Project Manager is primarily responsible for managing all endpoint adjudication processes for a clinical trial. Location: United States (Remote) What you will be doing: * Manages ...

ICON

Clinical Adjudication Project Lead

Blue Bell, PA · On-site +1

Clinical Adjudication Project Lead ICON is a global healthcare intelligence and clinical research ... Proficient in trial management systems and MS Project (or equivalent PM software). * Knowledge of ...

ICON

Clinical Adjudication Project Lead

Blue Bell, PA · On-site +1

Clinical Adjudication Project Lead ICON is a global healthcare intelligence and clinical research ... Proficient in trial management systems and MS Project (or equivalent PM software). * Knowledge of ...

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Clinical Trial Adjudication information

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How much do clinical trial adjudication jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for clinical trial adjudication in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What is clinical trial adjudication?

Clinical trial adjudication is a process in which an independent committee reviews and evaluates specific events or outcomes reported during a clinical trial to ensure consistency, accuracy, and impartiality. This process helps minimize bias and ensures that endpoints, such as adverse events or diagnoses, are assessed according to predefined criteria. Adjudication is particularly important in trials where outcomes may be subjective or require expert interpretation, such as cardiovascular events or cancer diagnoses. The results from adjudication are used to support the credibility and reliability of the trial findings.

What are the key skills and qualifications needed to thrive in clinical trial adjudication, and why are they important?

To thrive in Clinical Trial Adjudication, you need a strong background in clinical research, medical terminology, and regulatory compliance, often supported by a degree in medicine, pharmacy, or life sciences. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and knowledge of Good Clinical Practice (GCP) guidelines and relevant certifications are typically required. Attention to detail, critical thinking, and effective communication are essential soft skills for reviewing complex case data and collaborating with cross-functional teams. These skills ensure accurate, unbiased event adjudication, maintaining data integrity and regulatory compliance throughout clinical trials.

What are some common challenges faced in a clinical trial adjudication role, and how can they be addressed?

A common challenge in Clinical Trial Adjudication is ensuring consistent and unbiased evaluation of clinical events across multiple adjudicators and sites. This often involves navigating complex medical data and adhering strictly to protocol-specific criteria, which can vary between studies. Effective communication, standardized training, and robust documentation processes are essential to maintain objectivity and data integrity. Collaborating closely with clinical operations, biostatistics, and regulatory teams also helps streamline the adjudication process and resolve discrepancies efficiently.

What is the difference between Clinical Trial Adjudication vs Clinical Research Coordinator?

AspectClinical Trial AdjudicationClinical Research Coordinator
CredentialsTypically requires clinical or medical background, certifications like CCRP or CCRCRequires research-related education, often a bachelor's degree in health or science
Work EnvironmentWorks closely with clinical data, medical teams, and regulatory bodiesManages study logistics, patient recruitment, and data collection at research sites
Industry UsageUsed mainly in clinical trial phases to determine patient eligibility and adverse eventsUsed across all phases for study coordination and participant management

While both roles are integral to clinical research, Clinical Trial Adjudication focuses on reviewing and confirming patient data and adverse events, often requiring medical expertise. Clinical Research Coordinators handle the operational aspects of trials, including patient recruitment and data collection. Understanding these differences helps in choosing the right career path or job focus within clinical research.

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Clinical Trial Adjudication jobs near you
Infographic showing various Clinical Trial Adjudication job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Trial Physician, Cell Therapy

Jobtailor

Princeton, NJ • On-site

$250/hr

Other

Posted 3 days ago

New

Job description


  • Manage evidence generation for the cell therapy portfolio, including Medical Affairs Sponsored studies (MAST)

  • Provide primary medical/clinical accountability and oversight for MAST aligned with Integrated Evidence Plans

  • Work with Worldwide Medical Cell Therapy Asset Lead, Cell Therapy MEG Lead, and study team members on day-to‑day oversight and conduct of clinical studies

  • Lead and participate in cross-functional matrix leadership teams

  • Source research concepts addressing critical evidence gaps for early and late assets in prioritized indications

  • Provide medical/clinical oversight for interventional and non-interventional medical affairs-sponsored studies

  • Collaborate on development of study protocols and informed consent forms, authoring and providing medical input

  • Support study execution, including clinical database development, clinical data oversight, site activation, enrollment status, and adjudication of protocol violations and deviations

  • Assess key safety‑related serious adverse events with Worldwide Patient Safety and oversee safety narratives when applicable

  • Conduct medical data review, including eligibility assessment and interpretation of trial data results

  • Oversee study‑related work performed by external CRO partners, particularly medical monitoring activities

  • Provide continuous medical education and protocol‑specific training to study teams, investigators, CROs, and others

  • Provide medical expertise during Study Steering Committees, Investigators' Meetings, and other study‑related meetings

  • Build relationships with principal investigators and external stakeholders

  • Partner with Medical stakeholders, including Clinical Research Collaborations, to ensure portfolio cohesiveness and one MEG voice

  • Fulfill GCP and compliance obligations and maintain required training

  • Apply business acumen and fiscal stewardship to create reciprocal scientific value and allocate resources aligned with company priorities


Requirements

  • 5-10 years of established strategic leadership experience in a pharmaceutical industry setting

  • In-depth understanding of Clinical Development, Medical Affairs, and Commercial functions related to the drug development process

  • MD required (or x‑US equivalent)

  • 2-3 years of clinical trial experience in an industry or academic setting

  • Expertise in the drug development process and clinical research

  • Experience with implementation and conduction of medical affairs‑led studies and/or cell therapy clinical development desirable

  • Ability to build credibility with external investigators and collaborative partners

  • Strong leadership behaviors, authenticity, agility, and an enterprise mindset

  • Demonstrated ability to develop and sustain a high‑performing team and lead teams, including matrix colleagues

  • Proven track record of leadership in a complex, matrix environment

  • Exceptional communication and interpersonal skills to influence decision‑making at all organizational levels

  • Ability to fulfill GCP and compliance obligations and maintain required training

  • Expected travel of approximately 20%-30% within the US


Core Competencies

Demonstrates expertise in Clinical Development and Medical Affairs, with a strong focus on managing evidence generation for cell therapy portfolios and leading cross‑functional teams. Proven ability to oversee clinical studies, ensure compliance with GCP, and build relationships with external stakeholders.


Highest-signal resume keywords

  • Clinical Development Expertise

  • Medical Affairs Leadership

  • GCP Compliance

  • Clinical Trial Experience

  • Cell Therapy Knowledge


ATS Optimization Keywords
Hard Skills

  • Clinical Data Oversight

  • Study Protocol Development

  • Medical Monitoring

  • Safety Data Review

  • Evidence Generation Management

  • Clinical Database Development

  • Adjudication of Protocol Violations

  • Medical Input Authoring

  • Enrollment Management

  • Interventional Study Oversight


Soft Skills

  • Leadership

  • Interpersonal Skills

  • Communication

  • Collaboration

  • Agility


Certifications & Qualifications

  • MD or x‑US Equivalent


Industry Keywords

  • Pharmaceutical Industry

  • Clinical Research

  • Medical Affairs

  • Drug Development Process

  • Matrix Leadership

  • Principal Investigator Relationships

  • CRO Management

  • Study Steering Committees

  • Investigator's Meetings

  • Compliance Obligations

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