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Clinical Trial Report Reviewer Jobs (NOW HIRING)

Actalent

Clinical Trial Associate

Bala Cynwyd, PA · On-site

$31.50 - $43/hr

Clinical Trial Associate The Clinical Trial Associate (CTA) supports the Director of Clinical ... Review Boards (IRBs) as needed to support submissions, approvals, and ongoing reporting. * Assist ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... This could include a review of monitoring reports and source document review. * Maintain study ...

Actalent

Clinical Trial Associate

Bala Cynwyd, PA · On-site

$31.50 - $43/hr

Clinical Trial Associate The Clinical Trial Associate (CTA) supports the Director of Clinical ... Review Boards (IRBs) as needed to support submissions, approvals, and ongoing reporting. * Assist ...

Verastem

Clinical Trial Manager

Boston, MA · On-site

$100K - $125K/yr

Summary: We are seeking a Clinical Trial Manager with experience in managing a global Phase 3 ... Oversee monitoring activities at clinical CROs by reviewing monitoring visit reports, protocol ...

Aerogen Ltd

Clinical Trial Manager

Morrisville, NC · On-site

... and reports to senior management on request. • Participate in ongoing study data reviews and ... clinical trial staff on study specific processes. • Other responsibilities as assigned. What ...

Frontier Medicines

Clinical Trial Manager

Boston, MA · Hybrid

$120K - $150K/yr

Monitor study performance metrics, timelines, and deliverables, and review CRO trip reports for ... Coordinate Clinical Trial Team meetings and drive action item follow-up. Maintain clinical ...

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Clinical Trial Report Reviewer information

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How much do clinical trial report reviewer jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for clinical trial report reviewer in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What does a clinical trial report reviewer do?

A Clinical Trial Report Reviewer is responsible for evaluating and ensuring the accuracy, completeness, and compliance of clinical trial reports before submission to regulatory authorities. They review documents for clarity, consistency, and adherence to regulatory guidelines like ICH-GCP. This role is crucial for maintaining the integrity of clinical data and supporting the drug approval process. Reviewers often collaborate with clinical researchers, medical writers, and regulatory teams to address any issues or discrepancies found during the review.

What are the key skills and qualifications needed to thrive as a clinical trial report reviewer?

To thrive as a Clinical Trial Report Reviewer, a strong background in clinical research, scientific writing, and regulatory guidelines such as ICH-GCP, often supported by a relevant life sciences degree, is essential. Familiarity with tools like electronic data capture (EDC) systems, document management platforms, and experience with regulatory submission standards are typically required. Attention to detail, critical thinking, and effective communication are key soft skills for ensuring accuracy and clarity in reports. These competencies are crucial for maintaining compliance, ensuring data integrity, and supporting successful regulatory submissions.

What are some common challenges faced by clinical trial report reviewers, and how can they be addressed?

Clinical Trial Report Reviewers often encounter challenges such as tight deadlines, managing complex data sets, and ensuring regulatory compliance. Staying current with evolving guidelines and collaborating closely with cross-functional teams, such as statisticians and medical writers, can help address these challenges. Good organizational skills, attention to detail, and clear communication are essential for meeting quality standards and supporting successful trial submissions.

What is the difference between Clinical Trial Report Reviewer vs Clinical Research Associate?

AspectClinical Trial Report ReviewerClinical Research Associate
Required CredentialsBachelor's degree, knowledge of regulatory guidelinesBachelor's degree, often with clinical research certification
Work EnvironmentReviewing clinical trial reports, data analysisMonitoring clinical sites, coordinating trials
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, academic institutions
Common Search & Comparison IntentUnderstanding report review roles, responsibilitiesUnderstanding trial monitoring, site management

The Clinical Trial Report Reviewer primarily focuses on analyzing and reviewing clinical trial reports to ensure accuracy and compliance. In contrast, the Clinical Research Associate is involved in monitoring clinical trial sites and coordinating data collection. Both roles are essential in clinical research, often working together within the same industry environments, but they have distinct responsibilities and skill sets.

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Clinical Trial Report Reviewer jobs near you
Infographic showing various Clinical Trial Report Reviewer job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Clinical Trial Manager (contract)

ALX Oncology Inc.

South San Francisco, CA

$90/hr

Contractor

Posted 14 days ago

Job description

Reporting to the Executive Director, Clinical Operations, the contract Clinical Trial Manager (CTM) will manage the day-to-day operational execution of global clinical trials from study start-up through closeout. The contract CTM will be responsible for coordinating study activities, managing timelines and vendors, monitoring study and site performance, and working across functions to ensure study milestones and deliverables are achieved on time and to a high standard of quality.

This is a 6- to 12-month contract assignment offering approximately 40 hours per week. The anticipated pay rate is approximately $90 per hour for candidates in the San Francisco Bay Area. Candidates who can work onsite in South San Francisco on Mondays and Tuesdays as part of the company's hybrid work model will be given preference. ADC clinical trial experience strongly preferred.

Qualified contractors should have experience that includes:

  • Managing day-to-day global clinical trial activities from study start-up through conduct and closeout, including timelines, milestones, enrollment, and study performance.
  • Supporting protocol review, feasibility assessments, site selection and activation, and protocol amendment activities.
  • Managing CROs, sites, and clinical vendors, including oversight of plans, deliverables, timelines, budgets, and quality.
  • Overseeing monitoring activities, including monitoring report review, U.S. co-monitoring, site performance, protocol deviations, data queries, and follow-up of significant issues.
  • Identifying operational risks and working cross-functionally to develop and implement mitigation strategies.
  • Leading study team meetings and communicating study progress, risks, decisions, and action items to internal and external stakeholders.
  • Ensuring study conduct and TMF quality are consistent with study protocols, ICH/GCP, applicable regulatory requirements, and inspection-readiness expectations.
  • Clinical operations experience in biotechnology, pharmaceutical, or CRO environments; ADC clinical trial experience strongly preferred.
  • Strong project management, communication, problem-solving, and organizational skills; proficiency with EDC, IRT, CTMS, and eTMF.
  • Ability to work effectively in a small, fast-paced biotech environment.

 

About ALX Oncology

ALX Oncology (Nasdaq: ALXO) is a clinical-stage biotechnology company advancing a pipeline of novel therapies designed to treat cancer and extend patients' lives. ALX Oncology's lead therapeutic candidate, evorpacept, has demonstrated potential to serve as a cornerstone therapy upon which the future of immuno-oncology can be built. Evorpacept is currently being evaluated across multiple ongoing clinical trials in a wide range of cancer indications. ALX Oncology's second pipeline candidate, ALX2004, is a novel EGFR-targeted antibody-drug conjugate with a differentiated mechanism of action. A Phase 1, dose-escalation trial of ALX2004 is ongoing in patients with EGFR-expressing solid tumors. More information is available at www.alxoncology.com and on LinkedIn @ALX Oncology.

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